Photocatalysis has emerged as an effective approach to sustainably convert biomass into value-added products.CoSe_(2)is a promising nonprecious,efficient cocatalyst for photooxidation,which can facilitate the separati...Photocatalysis has emerged as an effective approach to sustainably convert biomass into value-added products.CoSe_(2)is a promising nonprecious,efficient cocatalyst for photooxidation,which can facilitate the separation of photogenerated electron–holes,increase the reaction rates,and enhance photocatalytic efficiency.In this work,we synthesized a stable and efficient photocatalysis system of CoSe_(2)/g-C_(3)N_(4)through attaching CoSe_(2)on g-C_(3)N_(4)sheets,with a yield of 50.12%for the selective photooxidation of xylose to xylonic acid.Under light illumination,the photogenerated electrons were prone to migrating from g-C_(3)N_(4)to CoSe_(2)due to the higher work function of CoSe_(2),resulting in the accelerated separation of photogenerated electron–holes and the promoted photooxidation.Herein,this study reveals the unique function of CoSe_(2),which can significantly promote oxygen adsorption,work as an electron sink and accelerate the generation of ·O_(2)^(-),thereby improving the selectivity toward xylonic acid over other by-products.This work provides useful insights into the design of selective photocatalysts by engineering g-C_(3)N_(4)for biomass high-value utilization.展开更多
Background:Gallic acid(GA),a plant-derived polyphenol,possesses diverse biological functions such as reducing inflammation and against tumors.Currently,the influence of GA on the resistance of esophageal squamous cell...Background:Gallic acid(GA),a plant-derived polyphenol,possesses diverse biological functions such as reducing inflammation and against tumors.Currently,the influence of GA on the resistance of esophageal squamous cell carcinoma(ESCC)cells to cisplatin(DDP)is not well understood.Methods:Cell counting kit-8 assay examined how GA affected KYSE30 and TE-1 cell viability.5-Ethynyl-2′-deoxyuridine and TdT-mediated dUTP Nick-End labeling staining detected cell proliferation and apoptosis.Clone formation assay,flow cytometry,Carboxyfluorescein diacetate succinimidyl ester fluorescent probes,and Transwell assay determined cell biological properties,and 2′,7′-Dichlorofluorescin diacetate(DCFH-DA)fluorescent probes detected oxidative stress levels.Signal transducer and activator of transcription 3(STAT3)/Notch pathway protein levels after GA and/or Interleukin-6(IL-6)intervention were examined through Western blot.Furthermore,a model for subcutaneous graft tumors was established in nude mice.Results:GA exerted suppressive effects on cell proliferation,and caused apoptosis of KYSE30 and TE-1 cells.IL-6 intervention activated the STAT3/Notch pathway and promoted the malignant biological properties of ESCC cells.In contrast,GA attenuated the effects of IL-6,while STAT3 or Notch inhibitor further enhanced the effects of GA,suggesting that GA inhibited the IL-6/STAT3/Notch pathway.Not only that,GA promoted oxidative stress and enhanced cell sensitivity to DDP both in vitro and in vivo.Conclusion:GA suppresses the malignant progression of ESCC and enhances cell sensitivity to DDP by hindering the IL-6/STAT3/Notch pathway.展开更多
Dietary supplementation with plant-derivedα-linolenic acid(ALA)has the potential to alleviate the insufficient intake of global n-3 long-chain polyunsaturated fatty acids(n-3 LCPUFAs),but faces the bottleneck of high...Dietary supplementation with plant-derivedα-linolenic acid(ALA)has the potential to alleviate the insufficient intake of global n-3 long-chain polyunsaturated fatty acids(n-3 LCPUFAs),but faces the bottleneck of highβ-oxidation consumption,oxidative susceptibility,and low conversion efficiency.The current study investigated how flax lignans with different degrees of polymerization and glycosylation affect the conversion of ALA to n-3 LCPUFAs in mice over 35 days of administering sunflower phospholipid-stabilized flaxseed oil nanoemulsions.Results showed that flax lignan macromolecules(FLM)increased hepatic protein expression of elongase of very long chain fatty acid 5(Elovl5,24.2%)and fatty acid desaturase 2(Fads2,44.7%),thereby positively regulating ALA conversion pathways and raising serum eicosapentaenoic acid(EPA)levels(52.7%)via liver lipid re-efflux.Secoisolariciresinol diglucoside(SDG)enhanced ALA desaturation by upregulating hepatic protein expression of Fads1(30.4%)and Fads2(45.6%),increasing serum EPA levels(55.9%)and hepatic docosahexaenoic acid(DHA)levels(10%).Secoisolariciresinol(SECO)elevated hepatic protein expression of Elovl2(30.7%),Elovl5(11.7%),Fads1(37.9%),and Fads2(24.1%),but also increased carnitine palmitoyltransferase 1a(45.2%),leading to decreased ALA,EPA,and DHA levels in serum and liver.Therefore,in comparison,FLM and SDG emerge as the dominant structural units that positively regulate the conversion of ALA.These findings lay a groundwork for designing precise dietary delivery systems to enhance the conversion to n-3 LCPUFAs.展开更多
Patients with glioma have a very high mortality rate,thus improving the poor prognosis of glioma has been the goal in the therapeutic field.Searching for more effective drugs for gliomas from natural compounds is a pr...Patients with glioma have a very high mortality rate,thus improving the poor prognosis of glioma has been the goal in the therapeutic field.Searching for more effective drugs for gliomas from natural compounds is a promising strategy.In this study,both oleanonic acid and oleanolic acid inhibited proliferation of glioma cells and reduced expression of cyclin D1 and E1,but the former has a lower IC_(50)than the latter.Oleanonic acid reduced the expression of p-STAT3 but not p-STAT1 and 5,and also reducing the expression of STAT3 in the nucleus and its transcriptional activity in glioma cells.Furthermore,knockdown of STAT3 expression inhibited proliferation and migration of glioma cells.Next,the expressions of the upstream regulators such as SIRT6 and p-JAK2 but not SIRT1,p-ERK1/2,p300 were increased by oleanonic acid.The overexpression of SIRT6 not only reduced the expression of p-STAT3 and its transcriptional activity but also inhibited the proliferation and migration of glioma cells.In addition,the effects that oleanonic acid reduced the expression of p-STAT3 and its transcriptional activity and inhibited the proliferation and migration were attenuated by the knockdown of SIRT6.Furthermore,oleanonic acid effectively suppressed glioma growth and extended survival in nude mice bearing intracerebral U87 xenografts,but not in nude mice bearing intracerebral SIRT6-knockdown U87xenografts.In conclusion,oleanonic acid upregulates the expression of SIRT6 to inactivates STAT3 and then inhibits glioma growth.展开更多
Background Intestinal oxidative stress serves as an endogenous host defense against the gut microbiota by increas-ing energy expenditure and therefore decreasing feed efficiency(FE).Several systems coordinately regula...Background Intestinal oxidative stress serves as an endogenous host defense against the gut microbiota by increas-ing energy expenditure and therefore decreasing feed efficiency(FE).Several systems coordinately regulate redox bal-ance,including the mitochondrial respiratory chain,nicotinamide adenine dinucleotide phosphate(NADPH)oxidase,and different antioxidants.However,it remains unclear which redox balance compartments in the intestine are crucial for determining FE.Results In this study,we first screened the key targets of different metabolites and redox balance-related gene expression in broiler ceca.We then constructed a mouse colitis model to explore malic acid(MA)ability to allevi-ate intestinal inflammation.We further used controlled release technology to coat MA and investigated its effects on the intestinal redox status and FE in vivo.Finally,we examined the underlying mechanism by which MA modulated redox status using a porcine intestinal epithelial cell jejunum 2(IPEC-J2)cell model in vitro.Our results demonstrated that the MA/malic enzyme 3(ME3)pathway may play an important role in reducing oxidative stress in the broiler cecum.In addition,colon infusion of MA attenuated inflammatory phenotypes in the dextran sulfate sodium salt(DSS)induced mouse colitis model.Then,dietary supplementation with controlled-release MA pellet(MAP)reduced the feed to gain(F/G)ratio and promoted chicken growth,with reduced oxidative stress and increased bacterial diver-sity.Finally,the in vitro IPEC-J2 cell model revealed that ME3 mediated the effect of MA on cellular oxidative stress.Conclusion In summary,our study firstly revealed the important role of the MA/ME3 system in the hindgut of broiler chickens for improving intestinal health and FE,which may also be crucial for the implications of colon inflammation associated diseases.展开更多
Background:The purpose of this report is to summarize the evidence supporting supplementation of n-3 polyunsaturated fatty acids(n-3 PUFAs)in adult cancer patients,and to offer a better understanding of the appropriat...Background:The purpose of this report is to summarize the evidence supporting supplementation of n-3 polyunsaturated fatty acids(n-3 PUFAs)in adult cancer patients,and to offer a better understanding of the appropriate use of n-3 PUFAs in the clinical setting.Methods:Numerous databases were searched for guidelines,clinical decision-making documents,systematic reviews,expert consensus statements,and best evidence summaries about the use of n-3 PUFAs in cancer patients from the inception of the database to December 31,2023.Evidence grading and recommendation rating were conducted.The data extracted included the timing of supplementation,symptom management,disease prevention,cost-effectiveness,route of administration,application scenarios,dosage,and safety.Results:The collected data show that n-3 PUFAs are safe for patients receiving chemotherapy who are at risk of malnutrition and cachexia.Moreover,n-3 PUFA supplementation can alleviate the adverse symptoms associated with chemotherapy,extend survival,and improve the quality of life of patients with cancer.Conclusions:The administration of supplementary n-3 PUFAs should be considered based on the patient’s disease stage,treatment plan,nutritional status,and tolerance,as well as the dosage,route and application scenarios.Promoting the clinical use of n-3 PUFAs may improve the outcomes for patients with cancer.展开更多
Objective:To investigate the protective effect of ursolic acid(UA)on isoproterenol(ISO)-induced kidney injury in mice.Methods:Four groups of mice were used:GroupⅠ(Control)received phosphate-buffered saline i.p.for fo...Objective:To investigate the protective effect of ursolic acid(UA)on isoproterenol(ISO)-induced kidney injury in mice.Methods:Four groups of mice were used:GroupⅠ(Control)received phosphate-buffered saline i.p.for four weeks;GroupⅡ(ISO alone)was administered ISO(10 mg/kg i.p.)daily for four weeks to induce kidney injury;GroupⅢ(ISO+UA)was pretreated with UA(40 mg/kg i.p.)once daily,followed by ISO(10 mg/kg i.p.)once daily for four weeks;GroupⅣ(UA alone)received UA(40 mg/kg i.p.)daily for four weeks.Markers of oxidative stress,inflammation,and apoptosis were analyzed,and the protein expression of p-PI3K and p-Akt was determined.Results:UA treatment significantly alleviated ISO-induced kidney injury,evidenced by lowered levels of malondialdehyde,IL-6,TNF-αand IL-1β,downregulated expression of cleaved caspase-3 and PARP,and upregulated expression of Bcl-2 and Bcl-xL.It also activated the PI3K/Akt pathway.Conclusions:UA demonstrates renoprotective effects against ISO-induced kidney injury by reducing oxidative stress,inflammation,and apoptosis,likely through PI3K/Akt pathway activation.These findings suggest that UA may serve as a potential therapeutic agent for renal diseases linked to inflammation and oxidative stress,meriting further exploration for clinical applications.展开更多
The aim of this paper was to study the effect of combination of Lactobacillus strains and tryptophan(Trp)-rich diet on the intestinal barrier function of Balb/c mice exposed to a cocktail of antibiotics and dextran so...The aim of this paper was to study the effect of combination of Lactobacillus strains and tryptophan(Trp)-rich diet on the intestinal barrier function of Balb/c mice exposed to a cocktail of antibiotics and dextran sodium sulfate.Several Lactobacillus strains isolated from the healthy human fecal sample was found to utilize Trp to produce indole derivatives.The results of Trp metabolism indicated that the ability of Lactobacillus to metabolize Trp to produce indole-3-lactic acid(ILA),indole-3-carboxaldehyde(I3C),and indole-3-acetic acid varies in vitro and in vivo.The effect of Lactobacillus with high-yielding indole derivatives on disease activity index,colon length,and intestinal permeability was significantly better than that of Lactobacillus with low-yielding indole derivatives in a high Trp diet.And Lactobacillus combined with Trp intervention also had a certain regulatory effect on the intestinal flora of male BALB/c mice.Among them,Lactiplantibacillus plantarum DPUL-S164 produced more ILA both in vivo and in vitro,and the combination of L.plantarum DPUL-S164 and Trp significantly decreased the expression level of the serum pro-inflammatory cytokine interleukin(IL)-6 and increased the expression level of the anti-inflammatory cytokine IL-10,significantly improved the number of goblet cells in the mouse mucous layer and increased mucin and tight junction protein expression.Furthermore,L.plantarum DPUL-S164 combined with Trp intervention activated the aryl hydrocarbon receptors(Ah R)signaling pathway.Furthermore,we found that the expression of colonic tight junction protein was positively correlated with the expression of colonic Ah R,and the expression of Ah R was positively correlated with the concentrations of ILA and I3C in vivo.Therefore,we conclude that the ILA as Ah R ligand produced by L.plantarum DPUL-S164 regulated the Ah R pathway,thus up-regulating the expression of the tight junction protein and protecting the integrity of the epithelial barrier.展开更多
CALCINEURIN B-LIKE PROTEINS(CBLs)function in osmotic stress responses,root morphogenesis and ion uptake in various plants such as Arabidopsis.However,the roles of Os CBLs in regulating root growth in rice(Oryza sativa...CALCINEURIN B-LIKE PROTEINS(CBLs)function in osmotic stress responses,root morphogenesis and ion uptake in various plants such as Arabidopsis.However,the roles of Os CBLs in regulating root growth in rice(Oryza sativa),whose root morphology and growth environment strongly differ from those of Arabidopsis,are unknown.Here,we demonstrated that Os CBL3 functioned as a calcium sensor to regulate primary and lateral root development in rice.Os CBL3 interacted with Os CIPK31 in vivo and in vitro,and the loss of function of Os CBL3 or Os CIPK31 resulted in shorter roots and diminished lateral root growth.Overexpression of Os CIPK31 compensated for the root growth defects of Os CBL3 knockout mutants.These results demonstrated that the Os CBL3–Os CIPK31 module coordinated root development via the abscisic acid(ABA)and auxin pathways,as ABA inhibitors and low auxin concentrations partially rescued the short-root phenotype of their respective knockout lines.CYCLOPHYLIN 2(Os CYP2),a key factor in lateral root initiation and root growth maintenance,was phosphorylated by Os CIPK31,and knockout of Os CYP2 in Os CIPK31 overexpression lines resulted in a phenotype similar to that of Os CYP2 single knockout lines.Therefore,the Os CBL3–Os CIPK31 module functioned in ABA and auxin signal transduction,ensuring proper root growth.Os CIPK31,activated by Os CBL3,then phosphorylated Os CYP2,which drove primary and lateral root development.These results establish a new module regulating primary and lateral root development in rice.展开更多
Objective Tumour cells in a hypoxic state are more invasive,have stronger self-renewal capabilities,and are difficult to treat because of their ability to promote tumour recurrence and metastasis.The glycolysis inhibi...Objective Tumour cells in a hypoxic state are more invasive,have stronger self-renewal capabilities,and are difficult to treat because of their ability to promote tumour recurrence and metastasis.The glycolysis inhibitor 3-bromopyruvic acid(3-BrPA)can completely inactivate glycolytic enzymes at extremely low drug concentrations,thereby exerting a strong inhibitory effect on the glucose energy metabolism of tumor cells.Therefore,we tested the inhibitory effect of 3-BrPA on hepatocellular carcinoma cells(HepG2)in vitro;then,we used the VX2 liver cancer model to study the antitumour effect of 3-BrPA combined with interventional embolization on liver cancer.Methods In vitro,a CCK-8 assay was used to detect the inhibitory effect of different concentrations of 3-BrPA on HepG2 cells,and light microscopy confirmed that the HepG2 cells were completely dead.Western blotting was used to detect the expression of key proteins involved in apoptosis.A total of 30 New Zealand white rabbits were used to establish a liver cancer model and were randomly divided into 3 groups 2 weeks after tumor establishment:the control group was perfused with saline in the hepatic artery;the transcatheter arterial embolization(TAE)group was given TAE;and the experimental group was perfused with 3-BrPA combined with TAE.The tumor-bearing rabbits were killed one week after surgery.The tumor volume and tumor necrosis ratio were calculated via the histopathological examination.Results In vitro,the inhibitory effect of 3-BrPA on HepG2 cells increased with increasing concentration.3-BrPA(100μmol/L)could induce the necrosis of HepG2 cells.Stimulation with 50μmol/L 3-BrPA could activate the tumor cell apoptosis pathway.3-BrPA combined with TAE treatment could significantly inhibit tumor growth and cause more complete tumor necrosis.Conclusion 3-BrPA not only has antitumour effects in vitro but can also significantly improve antitumour effects in the hypoxic microenvironment after embolization in vivo.展开更多
Herein,a modified screen printed carbon electrode(SPCE)based on a composite material,graphene oxide-gold nanoparticles(GO-AuNPs),and poly(3-aminobenzoic acid)(P3ABA)for the detection of paraquat(PQ)is introduced.The m...Herein,a modified screen printed carbon electrode(SPCE)based on a composite material,graphene oxide-gold nanoparticles(GO-AuNPs),and poly(3-aminobenzoic acid)(P3ABA)for the detection of paraquat(PQ)is introduced.The modified electrode was fabricated by drop casting of the GO-AuNPs,followed by electropolymerization of 3-aminobenzoic acid to achieve SPCE/GO-AuNPs/P3ABA.The morphology and microstructural characteristics of the modified electrodes were revealed by scanning electron microscopy(SEM)for each step of modification.The composite GO-AuNPs can provide high surface area and enhance electroconductivity of the electrode.In addition,the presence of negatively charged P3ABA notably improved PQ adsorption and electron transfer rate,which stimulate redox reaction on the modified electrode,thus improving the sensitivity of PQ analysis.The SPCE/GOAuNPs/P3ABA offered a wide linear range of PQ determination(10^(−9)-10^(−4) mol/L)and low limit of detection(LOD)of 0.45×10^(−9) mol/L or 0.116μg/L,which is far below international safety regulations.The modified electrode showed minimum interference effect with percent recovery ranging from 96.5%to 116.1%after addition of other herbicides,pesticides,metal ions,and additives.The stability of the SPCE/GO-AuNPs/P3ABA was evaluated,and the results indicated negligible changes in the detection signal over 9 weeks.Moreover,this modified electrode was successfully implemented for PQ analysis in both natural and tapped water with high accuracy.展开更多
In order to reveal the effect of 2-hydroxy-3-naphthyl hydroxamic acid(H205)on the flotation behavior and action mechanism of bastnaesite,single-mineral flotation experiments of bastnaesite were conducted.The flotation...In order to reveal the effect of 2-hydroxy-3-naphthyl hydroxamic acid(H205)on the flotation behavior and action mechanism of bastnaesite,single-mineral flotation experiments of bastnaesite were conducted.The flotation recovery of bastnaesites can be achieved more than 90%when the aeration rate is 40 mL/min,the rotational speed is 200 r/min,the H205 dosage is 120 mg/L,and the pulp pH ranges from 7 to 9.The action mechanism of H205 on the surface of bastnaesite was studied by simultaneous thermogravimetry and differential scanning calorimetry(TG-DSC),Zeta potential measurements,Fourier transform-infrared spectra(FT-IR)and X-ray photoelectron spectroscopy(XPS).These analysis results show that under suitable flotation conditions,H205 has an obvious adsorption phenomenon on the surface of bastnaesite.The adsorption involves electrostatic interactions and chemical interactions,namely H205 has a strong collecting ability of bastnaesite due to the synergism of electrostatic adsorption and chemical adsorption.This study systematically reveals the flotation behavior and adsorption mechanism of H205 on the surface of bastnaesite,and provides useful theoretical guidance for efficient flotation separation of bastnaesite.展开更多
BACKGROUND The incidence of malignant tumors in the digestive system is increasing and is a threat to human health.However,the long duration from tumor detection to radical resection,stress responses due to surgical t...BACKGROUND The incidence of malignant tumors in the digestive system is increasing and is a threat to human health.However,the long duration from tumor detection to radical resection,stress responses due to surgical trauma,and insufficient nu-tritional intake increases the risk of malnutrition,immune function reduction,postoperative complications,and intestinal dysfunction among patients.AIM To systematically investigate the association of parenteral nutrition enriched with n-3 polyunsaturated fatty acids(PUFAs)with the nutritional status of patients after gastrointestinal treatment.METHODS Randomized controlled trials associated with PUFA-enriched parenteral nutrition administration in patients with digestive system malignancies were retrieved from online databases such as PubMed,EMBASE,ScienceDirect,Cochrane Li-brary,China Knowledge Network,China VIP,Wanfang,and China Biomedical Literature Database,with the retrieval time from database inception to present.Two researchers independently extracted data.Each article’s bias risk was ass-essed by referring to the Cochrane Handbook version 5.3 criteria and RevMan5.4 was used for data analysis.RESULTS This meta-analysis involved six randomized controlled trials involving a total of 505 cases.Random-effects model analysis indicated remarkably better impro-vements in various inflammatory factors in the study group(P<0.05).Meta-analysis of nutritional indicators revealed that the study group had higher total protein,albumin,and prealbumin levels,as well as lower transferrin levels compared to the control group(P<0.05).Meanwhile,meta-analysis of T-cell subsets revealed no remarkable inter-group difference in post-treatment CD8+cells(P>0.05).Moreover,the meta-analysis identified a notably lower incidence of adverse reactions in the study group(P<0.05).CONCLUSION Administration of PUFAs helps improve the nutritional status of patients with digestive malignancies in the perioperative period.It promotes immune function recovery,reduces the inflammatory response,and decreases the risk of adverse effects.These beneficial effects make it worth investigating and promoting their use in ap-propriate patient populations.However,further validation via high-quality studies with long intervention time and extended follow-up periods is required.展开更多
Background Colitis caused by bacterial infection is a major global health challenge.Unfortunately,current treatment options are limited.We previously disclosed that L.reuteri SXDT-32 was enriched in the feces of an an...Background Colitis caused by bacterial infection is a major global health challenge.Unfortunately,current treatment options are limited.We previously disclosed that L.reuteri SXDT-32 was enriched in the feces of an ancient diarrhearesistant pig breed(Mashen pig)in China over 2500 years old.As diarrhea is often closely associated with intestinal inflammation,L.reuteri SXDT-32 was identified as a potential beneficial bacterium to prevent intestinal inflammation.However,the precise mechanisms involved remained unclear.Results Our tests showed that L.reuteri SXDT-32 alleviated colonic damage induced by pathogenic E.coli SKLAN202302 in weaned pigs by enhancing barrier integrity and inhibiting inflammation.The transcriptomics revealed that L.reuteri SXDT-32 protected against inflammatory injury by inhibiting the PI3K-AKT signaling pathway.Metabolite analysis indicated that the content of shikimic acid(SA)was substantially elevated in the colonic mucosa of L.reuteri SXDT-32-fed piglets(P<0.05).In addition,Liquid Chromatography-Mass Spectrometer(LC-MS)analysis showed significant increases in SA content in both the colonic chyme of L.reuteri SXDT-32-fed piglets and the supernatant of in vitro grown cultures of L.reuteri SXDT-32(P<0.05).Polymerase chain reaction(PCR)analysis identified gene aroE from L.reuteri SXDT-32,which is a key gene directly linked to SA synthesis,and elevated shikimate dehydrogenase(SD,encoded by aroE)was also detected in both L.reuteri SXDT-32 and the colonic mucosa of piglets fed L.reuteri SXDT-32(P<0.01).In vitro Caco-2 cell experiments demonstrated that SA,L.reuteri SXDT-32,and the supernatant from in vitro grown cultures of L.reuteri SXDT-32 exhibited comparable inhibitory effects on the PI3K-Akt pathway to those of the PI3K inhibitor LY294002.Conclusions L.reuteri SXDT-32 alleviated intestinal inflammation in piglets by producing SA that inhibits the PI3K-Akt pathway.This study provides an innovative approach for the treatment and prevention of colitis caused by bacterial infection.展开更多
Objectives:Colorectal cancer(CRC)is one of the most common cancers all over the world.The progression of CRC is associated with inflammation and disruptions in intestinal flora.3-O-Acetyl-11-keto-β-boswellic acid(AKB...Objectives:Colorectal cancer(CRC)is one of the most common cancers all over the world.The progression of CRC is associated with inflammation and disruptions in intestinal flora.3-O-Acetyl-11-keto-β-boswellic acid(AKBA)has been noted for its potent anti-inflammatory properties.However,the effect of AKBA on colon cancer caused by inflammation and its mechanism are not unclear.The study is to explore the effect of AKBA on CRC and its mechanism.Materials and Methods:Cell proliferation,(5-ethynyl-2′-deoxyuridine,EdU)-DNA synthesis assay and colony formation were used to assess the effect of AKBA on the proliferation of CRC cells.Flow cytometry was employed to analyze the cell cycle and apoptosis rate of cells treated with AKBA.RNA sequencing was done to explore the underlying mechanisms of AKBA.Western blot was used to assess the expression of key proteins in the nuclear factor kappa-B(NF-κB)signaling pathway after the treatment of AKBA.Real-time quantitative PCR(RT-qPCR),enzyme-linked immunosorbent assay(ELISA),and Meso Scale Discovery(MSD)assays were employed to check the anti-inflammation effects of AKBA on Lipopolysaccharide(LPS)-induced RAW264.7 cells and LPS-induced mouse model.Additionally,the Azoxymethane/Dextran sulfate sodium(AOM/DSS)-induced colitis-associated CRC model was used to evaluate the anti-CRC effect of AKBA.Gut microbiota profiling of fecal samples from CRC mice,both with and without AKBA treatment,was conducted through metagenomic sequencing analysis.Results:Our results showed that AKBA reduced the proliferation of HCT116 and SW620 cells,increased apoptosis of cells,and arrested the cell cycle at the G2/M phase.Results from RNA-seq showed that AKBA inhibited CRC by inhibiting the NF-κB signaling pathway and reducing cellular inflammation.Furthermore,AKBA reduced the levels of inflammatory cytokines,including tumor necrosis factor-α(TNF-α),Interferon-γ(IFN-γ),Interleukin-IL-12p70(IL-12p70),Interleukin-1β(IL-1β),and tumor necrosis factor-α(TNF-α)in both the spleen and serum of LPS-induced acute inflammation mice.Additionally,AKBA inhibited the development of AOM/DSS-induced colitis-associated colon cancer in mice and positively influenced gut microbiota.Conclusion:This study highlights the inhibitory effect of AKBA on colitis-associated CRC and reveals a novel aspect of its role in the remodeling of gut microbiota.These findings suggest that AKBA may be used as a potential therapeutic agent for CRC.展开更多
BACKGROUND Gastric cancer(GC)is a type of cancer which causes high cancer-related mortality.Surgical operation and systematic chemical therapies are primary choices for the treatment of GC patients with advanced stage...BACKGROUND Gastric cancer(GC)is a type of cancer which causes high cancer-related mortality.Surgical operation and systematic chemical therapies are primary choices for the treatment of GC patients with advanced stages,however,the 5-year overall survival is only around 30%.AIM To investigate the role of mesenchymal stem cell(MSC)-derived long non-coding RNAs(lncRNA)NKILA in fatty acid oxidation and chemoresistance in GC cells,mediated through the miR-485-5p/STAT3 pathway.METHODS GC cell lines(AGS and MKN45)were co-cultured with human bone marrowderived MSCs were cultured.The MSC identity was confirmed by flow cytometry(CD73,CD90,CD105>95%positive,CD34,CD45 negative).Co-culture of GC cells and MSCs was performed in Transwell plates,where MSCs were placed in the upper chamber and GC cells in the lower chamber for 72 hours.For transfections,pcDNA-NKILA vectors,shSTAT3,and miR-485-5p mimics were utilized.Colony formation,apoptosis assays(Annexin V/PI staining),sphere formation,and flow cytometry were performed to evaluate cell proliferation,stemness,and chemoresistance.qPCR was used to analyze gene expression(Sox2,Oct4,CD133,LIN28,NKILA),and Western blotting assessed protein levels of stemness markers.Luciferase reporter assays were conducted to confirm miR-485-5p/STAT3 interactions,and biotin-labeled RNA pulldown was used to assess RNA-protein binding.Fatty acid oxidation was evaluated using a CPT1 activity assay andβ-oxidation rate detection.ATP levels were measured to assess the energetic status of GC cells.Clinical GC tissue samples were collected from patients at our hospital for validation.RESULTS MSCs were found to enhance the stemness and chemoresistance of GC cells.Co-culturing MKN45 and AGS cells with MSCs significantly increased sphere-forming ability and the expression of key cancer stem cell markers(SOX2,Oct4,LIN28,CD133),indicating that MSCs promote stem-like properties.Flow cytometry confirmed an enrichment of CD44+and CD133+subpopulations in MSC-treated GC cells.Additionally,MSC co-culture reduced chemotherapy-induced apoptosis and enhanced cell proliferation,suggesting a protective role in chemotherapy resistance.MSC-derived lncRNA NKILA further promoted stemness and chemoresistance,enhancing expression of stem cell markers and protecting cells from oxaliplatin and 5-FU-induced apoptosis.MSC co-culture also induced fatty acid oxidation in GC cells,as shown by increased CPT1 activity,β-oxidation rates,and ATP levels.NKILA mediated these effects by upregulating STAT3,which was confirmed to regulate fatty acid oxidation and chemoresistance.NKILA’s interaction with miR-485-5p further promoted STAT3 expression and fatty acid oxidation,reinforcing its role in maintaining stemness and enhancing chemoresistance.CONCLUSION MSCs enhance the stemness and chemoresistance of GC cells by secreting lncRNA NKILA,which promotes fatty acid oxidation through STAT3 activation.NKILA modulates the miR-485-5p/STAT3 axis,thereby increasing energy metabolism and supporting cancer stem cell properties.Targeting NKILA or the miR-485-5p/STAT3 pathway offers potential therapeutic strategies to overcome chemoresistance in GC.展开更多
BACKGROUND Diabetic retinopathy(DR)is the leading cause of vision loss in patients with diabetes.The vascular endothelial growth factor(VEGF)pathway plays a critical role in the pathogenesis of DR,and ranibizumab,an a...BACKGROUND Diabetic retinopathy(DR)is the leading cause of vision loss in patients with diabetes.The vascular endothelial growth factor(VEGF)pathway plays a critical role in the pathogenesis of DR,and ranibizumab,an anti-VEGF agent,has shown promise in its treatment.Signal transducer and activator of transcription 3(STAT3)is involved in inflammatory processes and cellular signaling,while glial fibrillary acidic protein(GFAP)is a marker of glial cell activation,both contributing to retinal damage in DR.However,the mechanisms by which ranibizumab affect early-stage DR through the VEGF/STAT3/GFAP pathway are not fully understood.AIM To investigate the role of ranibizumab in early DR via the VEGF/STAT3/GFAP pathway.METHODS Adult retinal pigment epithelial 19(ARPE-19)cells and human retinal microvascular endothelial cells(HRMECs)were cultured under high-glucose conditions to simulate a diabetic environment.The effects of ranibizumab on cytokine mRNA and protein expression were analyzed by quantitative polymerase chain reaction and Western blot analysis.A diabetic rat model was induced with streptozotocin(60 mg/kg).Retinal changes,including retinal ganglion cell(RGC)apoptosis,vascular alterations,and cytokine expression,were evaluated using fundus fluorescein angiography,hematoxylin and eosin and periodic acid Schiff staining,immunofluorescence,confocal imaging,and Western blot analysis.RESULTS High-glucose conditions significantly increased the mRNA and protein levels of VEGF,STAT3,GFAP,and other cytokines in ARPE-19 and HRMECs.However,these levels were partially suppressed by ranibizumab.RGC apoptosis,vascular leakage,and elevated cytokine expression were observed during early-stage DR in diabetic rats.Ranibizumab treatment in diabetic rats reduced cytokine expression,restored RGCs,and repaired vascular networks.CONCLUSION Intravitreal ranibizumab modulates the VEGF/STAT3/GFAP pathway,suppresses cytokine expression,and promotes retinal repair,effectively delaying or preventing early DR progression.展开更多
BACKGROUND Improving our understanding of whether increased dietary intake ofω-3 polyunsaturated fatty acids(PUFAs)is beneficial for increasing skeletal muscle mass in patients with metabolic dysfunction-associated f...BACKGROUND Improving our understanding of whether increased dietary intake ofω-3 polyunsaturated fatty acids(PUFAs)is beneficial for increasing skeletal muscle mass in patients with metabolic dysfunction-associated fatty liver disease(MAFLD)could provide an important clinical evidence base for the development of relevant nutritional guidelines.AIM To investigate the effect of total dietaryω-3 PUFAs and their subtypes on skeletal muscle mass in MAFLD.METHODS This cross-sectional study involved 2316 participants from four National Health and Nutrition Examination Survey cycles between 2011 and 2018.Dietary intake ofω-3 PUFAs was collected through 24-hour dietary recall interviews.Appendicular skeletal muscle mass index(ASMI)was calculated by dividing ASM in kilograms by height squared.RESULTS The multiple linear regression model showed significant relationships for dietary intake of totalω-3 PUFAs with higher ASMI(β:0.06,95%CI:0.01-0.11)in MAFLD patients.Dietary a-linolenic acid(ALA)(β:0.06,95%CI:0.01-0.12),docosapentaenoic acid(β:1.28,95%CI:0.01-2.54),and docosahexaenoic acid(DHA)(β:0.19,95%CI:0.01-0.37)were significantly associated with higher ASMI,while intake of stearidonic acid and eicosapentaenoic acid did not improve ASMI.In patients with high probability of liver fibrosis,dietary intake of ALA was associated with higher ASMI(β:0.11,95%CI:0.03-0.18).Stratified analysis found that DHA was associated with higher ASMI in patients with obesity and higher metabolic risk.CONCLUSION Increasing dietary intake ofω-3 PUFAs improved skeletal muscle health in patients with MAFLD.Patient with obesity and higher metabolic risk were more likely to benefit from intake of DHA.展开更多
Triflumezopyrim(TFM)is a novel mesoionic pyrido[1,2-α]pyrimidinones insecticide,which acts on nicotinic acetylcholine receptors(n ACh Rs)and has no cross-resistance with other insecticides.Herein,we firstly developed...Triflumezopyrim(TFM)is a novel mesoionic pyrido[1,2-α]pyrimidinones insecticide,which acts on nicotinic acetylcholine receptors(n ACh Rs)and has no cross-resistance with other insecticides.Herein,we firstly developed a new continuous flow approach to synthesis 2-[3-(trifluoromethyl)phenyl]malonic acid,a key intermate of TFM,coupling with esterification,condensation,and hydrolysis.All three-step reactions were optimized and transformed into a continuous synthesis mode by three micro reaction units.Compared with the batch mode,the total reaction time and overall separation yield were improved from more than 12 h and 60%to 18 min and 73.38%,respectively.The solvent consumption and waste emission were significantly reduced,which also provides an eco-friendly and efficient potential tool for the development and production of mesoionic pyrido[1,2-α]pyrimidinones insecticide.展开更多
Ammonia Selective Catalytic Reduction(NHs-SCR)technology has been employed to eliminate NO_(x) from diesel engine exhaust,with Cu-SSZ-13 serving as the commercial catalyst.The greenhouse gas N_(2)O is produced as a by...Ammonia Selective Catalytic Reduction(NHs-SCR)technology has been employed to eliminate NO_(x) from diesel engine exhaust,with Cu-SSZ-13 serving as the commercial catalyst.The greenhouse gas N_(2)O is produced as a byproduct when using Cu-SSZ-13 as the NH_(3)-SCR catalyst.To achieve synergistic control of pollutants and greenhouse gases in diesel engine exhaust,rational design of Cu-SSZ-13 catalysts is required.In this study,the effect of Brønsted acid sites in Cu-SSZ-13 catalysts on the formation of N_(2)O was investigated.Mild thermal treatmentwas innovatively employed to prepare Cu-SSZ-13 catalysts with different amounts of Brønsted acid sites.EPR,H_(2)-TPR,NH_(3)-TPD,NMR were utilized to determine that the Brønsted acid sites were modified while the Cu species remained unchanged.Thereby an accurate assessment of the influence of Brønsted acid sites on N_(2)O formation could be achieved.Our results showed that Cu-SSZ-13 with more Brønsted acid sites produced less N_(2)O during the NH_(3)-SCR reaction.In the low-temperature region,the presence of framework acid sites facilitates the decomposition of the NH_(4)NO_(3)assisted by NO to form N_(2)and H_(2)O,reducing the formation of N_(2)O.In the high-temperature region,the Brønsted acid sites promote the decomposition of NH_(2)NO into N_(2)and H_(2)O.Meanwhile,the N_(2)O-SCR reaction can also be promoted by Brønsted acid sites,thereby decreasing N_(2)O emissions.This study suggests that in the future design and synthesis of Cu-SSZ-13 zeolites,attention should be paid to creating more Brønsted acid sites in Cu-SSZ-13 to reduce N_(2)O emissions.展开更多
基金financial support by National Key Research and Development Project(Grant No.2023YFE0109600)Guangzhou Key Research and Development Program(Grant No.2023B03J1330)+5 种基金National Program for Support of Topnotch Young Professionals(Grant No.x2qsA4210090)Guangzhou Basic and Applied Basic Research Foundation(Grant No.2024A04J3413)National Natural Science Foundation of China(Grant No.32201499)State Key Laboratory of Pulp and Paper Engineering(Grant Nos.2023PY01 and 202215)Guangdong Basic and Applied Basic Research Foundation(Grant Nos.2023A1515012519 and 2023B1515040013)China Postdoctoral Science Foundation(Grant No.2023M732021).
文摘Photocatalysis has emerged as an effective approach to sustainably convert biomass into value-added products.CoSe_(2)is a promising nonprecious,efficient cocatalyst for photooxidation,which can facilitate the separation of photogenerated electron–holes,increase the reaction rates,and enhance photocatalytic efficiency.In this work,we synthesized a stable and efficient photocatalysis system of CoSe_(2)/g-C_(3)N_(4)through attaching CoSe_(2)on g-C_(3)N_(4)sheets,with a yield of 50.12%for the selective photooxidation of xylose to xylonic acid.Under light illumination,the photogenerated electrons were prone to migrating from g-C_(3)N_(4)to CoSe_(2)due to the higher work function of CoSe_(2),resulting in the accelerated separation of photogenerated electron–holes and the promoted photooxidation.Herein,this study reveals the unique function of CoSe_(2),which can significantly promote oxygen adsorption,work as an electron sink and accelerate the generation of ·O_(2)^(-),thereby improving the selectivity toward xylonic acid over other by-products.This work provides useful insights into the design of selective photocatalysts by engineering g-C_(3)N_(4)for biomass high-value utilization.
基金Mechanistic Investigation into the Extraction,Purification,and Anti-Esophageal Cancer Effects of Gallic Acid Derived from Rhodiola crenulata(YLUKLM2023001).
文摘Background:Gallic acid(GA),a plant-derived polyphenol,possesses diverse biological functions such as reducing inflammation and against tumors.Currently,the influence of GA on the resistance of esophageal squamous cell carcinoma(ESCC)cells to cisplatin(DDP)is not well understood.Methods:Cell counting kit-8 assay examined how GA affected KYSE30 and TE-1 cell viability.5-Ethynyl-2′-deoxyuridine and TdT-mediated dUTP Nick-End labeling staining detected cell proliferation and apoptosis.Clone formation assay,flow cytometry,Carboxyfluorescein diacetate succinimidyl ester fluorescent probes,and Transwell assay determined cell biological properties,and 2′,7′-Dichlorofluorescin diacetate(DCFH-DA)fluorescent probes detected oxidative stress levels.Signal transducer and activator of transcription 3(STAT3)/Notch pathway protein levels after GA and/or Interleukin-6(IL-6)intervention were examined through Western blot.Furthermore,a model for subcutaneous graft tumors was established in nude mice.Results:GA exerted suppressive effects on cell proliferation,and caused apoptosis of KYSE30 and TE-1 cells.IL-6 intervention activated the STAT3/Notch pathway and promoted the malignant biological properties of ESCC cells.In contrast,GA attenuated the effects of IL-6,while STAT3 or Notch inhibitor further enhanced the effects of GA,suggesting that GA inhibited the IL-6/STAT3/Notch pathway.Not only that,GA promoted oxidative stress and enhanced cell sensitivity to DDP both in vitro and in vivo.Conclusion:GA suppresses the malignant progression of ESCC and enhances cell sensitivity to DDP by hindering the IL-6/STAT3/Notch pathway.
基金supported by grants from the National Natural Science Foundation of China(32072267)China Agriculture Research System(CARS-14)+1 种基金National Key Research and Development Program of China(2023YFD2100404)the Innovation Group Project of Hubei Province(2023AFA042).
文摘Dietary supplementation with plant-derivedα-linolenic acid(ALA)has the potential to alleviate the insufficient intake of global n-3 long-chain polyunsaturated fatty acids(n-3 LCPUFAs),but faces the bottleneck of highβ-oxidation consumption,oxidative susceptibility,and low conversion efficiency.The current study investigated how flax lignans with different degrees of polymerization and glycosylation affect the conversion of ALA to n-3 LCPUFAs in mice over 35 days of administering sunflower phospholipid-stabilized flaxseed oil nanoemulsions.Results showed that flax lignan macromolecules(FLM)increased hepatic protein expression of elongase of very long chain fatty acid 5(Elovl5,24.2%)and fatty acid desaturase 2(Fads2,44.7%),thereby positively regulating ALA conversion pathways and raising serum eicosapentaenoic acid(EPA)levels(52.7%)via liver lipid re-efflux.Secoisolariciresinol diglucoside(SDG)enhanced ALA desaturation by upregulating hepatic protein expression of Fads1(30.4%)and Fads2(45.6%),increasing serum EPA levels(55.9%)and hepatic docosahexaenoic acid(DHA)levels(10%).Secoisolariciresinol(SECO)elevated hepatic protein expression of Elovl2(30.7%),Elovl5(11.7%),Fads1(37.9%),and Fads2(24.1%),but also increased carnitine palmitoyltransferase 1a(45.2%),leading to decreased ALA,EPA,and DHA levels in serum and liver.Therefore,in comparison,FLM and SDG emerge as the dominant structural units that positively regulate the conversion of ALA.These findings lay a groundwork for designing precise dietary delivery systems to enhance the conversion to n-3 LCPUFAs.
基金supported by the National Natural Science Foundation of China(81560059,81760058,8160042,and 31800891)。
文摘Patients with glioma have a very high mortality rate,thus improving the poor prognosis of glioma has been the goal in the therapeutic field.Searching for more effective drugs for gliomas from natural compounds is a promising strategy.In this study,both oleanonic acid and oleanolic acid inhibited proliferation of glioma cells and reduced expression of cyclin D1 and E1,but the former has a lower IC_(50)than the latter.Oleanonic acid reduced the expression of p-STAT3 but not p-STAT1 and 5,and also reducing the expression of STAT3 in the nucleus and its transcriptional activity in glioma cells.Furthermore,knockdown of STAT3 expression inhibited proliferation and migration of glioma cells.Next,the expressions of the upstream regulators such as SIRT6 and p-JAK2 but not SIRT1,p-ERK1/2,p300 were increased by oleanonic acid.The overexpression of SIRT6 not only reduced the expression of p-STAT3 and its transcriptional activity but also inhibited the proliferation and migration of glioma cells.In addition,the effects that oleanonic acid reduced the expression of p-STAT3 and its transcriptional activity and inhibited the proliferation and migration were attenuated by the knockdown of SIRT6.Furthermore,oleanonic acid effectively suppressed glioma growth and extended survival in nude mice bearing intracerebral U87 xenografts,but not in nude mice bearing intracerebral SIRT6-knockdown U87xenografts.In conclusion,oleanonic acid upregulates the expression of SIRT6 to inactivates STAT3 and then inhibits glioma growth.
基金supported by the local innovative and research teams project of Guangdong province(2019BT02N630)national key research and development program(2022YFD1300401)+2 种基金Double first-class discipline promoting project(2023B10564001)National Natural Science Foundation of China(32272954)Natural Science Foundation of Guangdong Province,China(2024A1515013131).
文摘Background Intestinal oxidative stress serves as an endogenous host defense against the gut microbiota by increas-ing energy expenditure and therefore decreasing feed efficiency(FE).Several systems coordinately regulate redox bal-ance,including the mitochondrial respiratory chain,nicotinamide adenine dinucleotide phosphate(NADPH)oxidase,and different antioxidants.However,it remains unclear which redox balance compartments in the intestine are crucial for determining FE.Results In this study,we first screened the key targets of different metabolites and redox balance-related gene expression in broiler ceca.We then constructed a mouse colitis model to explore malic acid(MA)ability to allevi-ate intestinal inflammation.We further used controlled release technology to coat MA and investigated its effects on the intestinal redox status and FE in vivo.Finally,we examined the underlying mechanism by which MA modulated redox status using a porcine intestinal epithelial cell jejunum 2(IPEC-J2)cell model in vitro.Our results demonstrated that the MA/malic enzyme 3(ME3)pathway may play an important role in reducing oxidative stress in the broiler cecum.In addition,colon infusion of MA attenuated inflammatory phenotypes in the dextran sulfate sodium salt(DSS)induced mouse colitis model.Then,dietary supplementation with controlled-release MA pellet(MAP)reduced the feed to gain(F/G)ratio and promoted chicken growth,with reduced oxidative stress and increased bacterial diver-sity.Finally,the in vitro IPEC-J2 cell model revealed that ME3 mediated the effect of MA on cellular oxidative stress.Conclusion In summary,our study firstly revealed the important role of the MA/ME3 system in the hindgut of broiler chickens for improving intestinal health and FE,which may also be crucial for the implications of colon inflammation associated diseases.
文摘Background:The purpose of this report is to summarize the evidence supporting supplementation of n-3 polyunsaturated fatty acids(n-3 PUFAs)in adult cancer patients,and to offer a better understanding of the appropriate use of n-3 PUFAs in the clinical setting.Methods:Numerous databases were searched for guidelines,clinical decision-making documents,systematic reviews,expert consensus statements,and best evidence summaries about the use of n-3 PUFAs in cancer patients from the inception of the database to December 31,2023.Evidence grading and recommendation rating were conducted.The data extracted included the timing of supplementation,symptom management,disease prevention,cost-effectiveness,route of administration,application scenarios,dosage,and safety.Results:The collected data show that n-3 PUFAs are safe for patients receiving chemotherapy who are at risk of malnutrition and cachexia.Moreover,n-3 PUFA supplementation can alleviate the adverse symptoms associated with chemotherapy,extend survival,and improve the quality of life of patients with cancer.Conclusions:The administration of supplementary n-3 PUFAs should be considered based on the patient’s disease stage,treatment plan,nutritional status,and tolerance,as well as the dosage,route and application scenarios.Promoting the clinical use of n-3 PUFAs may improve the outcomes for patients with cancer.
文摘Objective:To investigate the protective effect of ursolic acid(UA)on isoproterenol(ISO)-induced kidney injury in mice.Methods:Four groups of mice were used:GroupⅠ(Control)received phosphate-buffered saline i.p.for four weeks;GroupⅡ(ISO alone)was administered ISO(10 mg/kg i.p.)daily for four weeks to induce kidney injury;GroupⅢ(ISO+UA)was pretreated with UA(40 mg/kg i.p.)once daily,followed by ISO(10 mg/kg i.p.)once daily for four weeks;GroupⅣ(UA alone)received UA(40 mg/kg i.p.)daily for four weeks.Markers of oxidative stress,inflammation,and apoptosis were analyzed,and the protein expression of p-PI3K and p-Akt was determined.Results:UA treatment significantly alleviated ISO-induced kidney injury,evidenced by lowered levels of malondialdehyde,IL-6,TNF-αand IL-1β,downregulated expression of cleaved caspase-3 and PARP,and upregulated expression of Bcl-2 and Bcl-xL.It also activated the PI3K/Akt pathway.Conclusions:UA demonstrates renoprotective effects against ISO-induced kidney injury by reducing oxidative stress,inflammation,and apoptosis,likely through PI3K/Akt pathway activation.These findings suggest that UA may serve as a potential therapeutic agent for renal diseases linked to inflammation and oxidative stress,meriting further exploration for clinical applications.
基金project was supported by the National Key Research and Development Program(2021YFD2100700)。
文摘The aim of this paper was to study the effect of combination of Lactobacillus strains and tryptophan(Trp)-rich diet on the intestinal barrier function of Balb/c mice exposed to a cocktail of antibiotics and dextran sodium sulfate.Several Lactobacillus strains isolated from the healthy human fecal sample was found to utilize Trp to produce indole derivatives.The results of Trp metabolism indicated that the ability of Lactobacillus to metabolize Trp to produce indole-3-lactic acid(ILA),indole-3-carboxaldehyde(I3C),and indole-3-acetic acid varies in vitro and in vivo.The effect of Lactobacillus with high-yielding indole derivatives on disease activity index,colon length,and intestinal permeability was significantly better than that of Lactobacillus with low-yielding indole derivatives in a high Trp diet.And Lactobacillus combined with Trp intervention also had a certain regulatory effect on the intestinal flora of male BALB/c mice.Among them,Lactiplantibacillus plantarum DPUL-S164 produced more ILA both in vivo and in vitro,and the combination of L.plantarum DPUL-S164 and Trp significantly decreased the expression level of the serum pro-inflammatory cytokine interleukin(IL)-6 and increased the expression level of the anti-inflammatory cytokine IL-10,significantly improved the number of goblet cells in the mouse mucous layer and increased mucin and tight junction protein expression.Furthermore,L.plantarum DPUL-S164 combined with Trp intervention activated the aryl hydrocarbon receptors(Ah R)signaling pathway.Furthermore,we found that the expression of colonic tight junction protein was positively correlated with the expression of colonic Ah R,and the expression of Ah R was positively correlated with the concentrations of ILA and I3C in vivo.Therefore,we conclude that the ILA as Ah R ligand produced by L.plantarum DPUL-S164 regulated the Ah R pathway,thus up-regulating the expression of the tight junction protein and protecting the integrity of the epithelial barrier.
基金the Sichuan Science and Technology Program(2023NSFSC1933,2022ZDZX0016,2021YFYZ0016)the Chengdu Science and Technology Bureau(2022-YF09-00036-SN)+1 种基金the free exploration project of the State Key Laboratory of Crop Gene Exploration and Utilization in Southwest China(SKL-ZY202214)the Changde Science and Technology Bureau(changkehan 2021–59)。
文摘CALCINEURIN B-LIKE PROTEINS(CBLs)function in osmotic stress responses,root morphogenesis and ion uptake in various plants such as Arabidopsis.However,the roles of Os CBLs in regulating root growth in rice(Oryza sativa),whose root morphology and growth environment strongly differ from those of Arabidopsis,are unknown.Here,we demonstrated that Os CBL3 functioned as a calcium sensor to regulate primary and lateral root development in rice.Os CBL3 interacted with Os CIPK31 in vivo and in vitro,and the loss of function of Os CBL3 or Os CIPK31 resulted in shorter roots and diminished lateral root growth.Overexpression of Os CIPK31 compensated for the root growth defects of Os CBL3 knockout mutants.These results demonstrated that the Os CBL3–Os CIPK31 module coordinated root development via the abscisic acid(ABA)and auxin pathways,as ABA inhibitors and low auxin concentrations partially rescued the short-root phenotype of their respective knockout lines.CYCLOPHYLIN 2(Os CYP2),a key factor in lateral root initiation and root growth maintenance,was phosphorylated by Os CIPK31,and knockout of Os CYP2 in Os CIPK31 overexpression lines resulted in a phenotype similar to that of Os CYP2 single knockout lines.Therefore,the Os CBL3–Os CIPK31 module functioned in ABA and auxin signal transduction,ensuring proper root growth.Os CIPK31,activated by Os CBL3,then phosphorylated Os CYP2,which drove primary and lateral root development.These results establish a new module regulating primary and lateral root development in rice.
基金National Natural Science Foundation of China(No.82202281)for the funding support,and Yu-miao Wei for his review of the manuscript.
文摘Objective Tumour cells in a hypoxic state are more invasive,have stronger self-renewal capabilities,and are difficult to treat because of their ability to promote tumour recurrence and metastasis.The glycolysis inhibitor 3-bromopyruvic acid(3-BrPA)can completely inactivate glycolytic enzymes at extremely low drug concentrations,thereby exerting a strong inhibitory effect on the glucose energy metabolism of tumor cells.Therefore,we tested the inhibitory effect of 3-BrPA on hepatocellular carcinoma cells(HepG2)in vitro;then,we used the VX2 liver cancer model to study the antitumour effect of 3-BrPA combined with interventional embolization on liver cancer.Methods In vitro,a CCK-8 assay was used to detect the inhibitory effect of different concentrations of 3-BrPA on HepG2 cells,and light microscopy confirmed that the HepG2 cells were completely dead.Western blotting was used to detect the expression of key proteins involved in apoptosis.A total of 30 New Zealand white rabbits were used to establish a liver cancer model and were randomly divided into 3 groups 2 weeks after tumor establishment:the control group was perfused with saline in the hepatic artery;the transcatheter arterial embolization(TAE)group was given TAE;and the experimental group was perfused with 3-BrPA combined with TAE.The tumor-bearing rabbits were killed one week after surgery.The tumor volume and tumor necrosis ratio were calculated via the histopathological examination.Results In vitro,the inhibitory effect of 3-BrPA on HepG2 cells increased with increasing concentration.3-BrPA(100μmol/L)could induce the necrosis of HepG2 cells.Stimulation with 50μmol/L 3-BrPA could activate the tumor cell apoptosis pathway.3-BrPA combined with TAE treatment could significantly inhibit tumor growth and cause more complete tumor necrosis.Conclusion 3-BrPA not only has antitumour effects in vitro but can also significantly improve antitumour effects in the hypoxic microenvironment after embolization in vivo.
基金supported by the ProgramManagement Unit on Area Based Development (PMUA),Thailand (No.4594393)the National Science and Technology Development Agency (NSTDA),Thailand (No.P2250367).
文摘Herein,a modified screen printed carbon electrode(SPCE)based on a composite material,graphene oxide-gold nanoparticles(GO-AuNPs),and poly(3-aminobenzoic acid)(P3ABA)for the detection of paraquat(PQ)is introduced.The modified electrode was fabricated by drop casting of the GO-AuNPs,followed by electropolymerization of 3-aminobenzoic acid to achieve SPCE/GO-AuNPs/P3ABA.The morphology and microstructural characteristics of the modified electrodes were revealed by scanning electron microscopy(SEM)for each step of modification.The composite GO-AuNPs can provide high surface area and enhance electroconductivity of the electrode.In addition,the presence of negatively charged P3ABA notably improved PQ adsorption and electron transfer rate,which stimulate redox reaction on the modified electrode,thus improving the sensitivity of PQ analysis.The SPCE/GOAuNPs/P3ABA offered a wide linear range of PQ determination(10^(−9)-10^(−4) mol/L)and low limit of detection(LOD)of 0.45×10^(−9) mol/L or 0.116μg/L,which is far below international safety regulations.The modified electrode showed minimum interference effect with percent recovery ranging from 96.5%to 116.1%after addition of other herbicides,pesticides,metal ions,and additives.The stability of the SPCE/GO-AuNPs/P3ABA was evaluated,and the results indicated negligible changes in the detection signal over 9 weeks.Moreover,this modified electrode was successfully implemented for PQ analysis in both natural and tapped water with high accuracy.
基金Project supported by the Natural Science Foundation Innovation Group Project of Hubei Province(2023AFA044)the National Natural Science Foundation of China(52222405)+1 种基金the Science and Technology Research Project of Education Department of Hubei Province(Q20221505)the China Postdoctoral Science(2023M731041)。
文摘In order to reveal the effect of 2-hydroxy-3-naphthyl hydroxamic acid(H205)on the flotation behavior and action mechanism of bastnaesite,single-mineral flotation experiments of bastnaesite were conducted.The flotation recovery of bastnaesites can be achieved more than 90%when the aeration rate is 40 mL/min,the rotational speed is 200 r/min,the H205 dosage is 120 mg/L,and the pulp pH ranges from 7 to 9.The action mechanism of H205 on the surface of bastnaesite was studied by simultaneous thermogravimetry and differential scanning calorimetry(TG-DSC),Zeta potential measurements,Fourier transform-infrared spectra(FT-IR)and X-ray photoelectron spectroscopy(XPS).These analysis results show that under suitable flotation conditions,H205 has an obvious adsorption phenomenon on the surface of bastnaesite.The adsorption involves electrostatic interactions and chemical interactions,namely H205 has a strong collecting ability of bastnaesite due to the synergism of electrostatic adsorption and chemical adsorption.This study systematically reveals the flotation behavior and adsorption mechanism of H205 on the surface of bastnaesite,and provides useful theoretical guidance for efficient flotation separation of bastnaesite.
基金Supported by the Guangxi Medical and Health Key(Cultivation)Discipline Construction ProjectGuilin Scientific Research and Technology Development Program Project,No.20210227-7-8.
文摘BACKGROUND The incidence of malignant tumors in the digestive system is increasing and is a threat to human health.However,the long duration from tumor detection to radical resection,stress responses due to surgical trauma,and insufficient nu-tritional intake increases the risk of malnutrition,immune function reduction,postoperative complications,and intestinal dysfunction among patients.AIM To systematically investigate the association of parenteral nutrition enriched with n-3 polyunsaturated fatty acids(PUFAs)with the nutritional status of patients after gastrointestinal treatment.METHODS Randomized controlled trials associated with PUFA-enriched parenteral nutrition administration in patients with digestive system malignancies were retrieved from online databases such as PubMed,EMBASE,ScienceDirect,Cochrane Li-brary,China Knowledge Network,China VIP,Wanfang,and China Biomedical Literature Database,with the retrieval time from database inception to present.Two researchers independently extracted data.Each article’s bias risk was ass-essed by referring to the Cochrane Handbook version 5.3 criteria and RevMan5.4 was used for data analysis.RESULTS This meta-analysis involved six randomized controlled trials involving a total of 505 cases.Random-effects model analysis indicated remarkably better impro-vements in various inflammatory factors in the study group(P<0.05).Meta-analysis of nutritional indicators revealed that the study group had higher total protein,albumin,and prealbumin levels,as well as lower transferrin levels compared to the control group(P<0.05).Meanwhile,meta-analysis of T-cell subsets revealed no remarkable inter-group difference in post-treatment CD8+cells(P>0.05).Moreover,the meta-analysis identified a notably lower incidence of adverse reactions in the study group(P<0.05).CONCLUSION Administration of PUFAs helps improve the nutritional status of patients with digestive malignancies in the perioperative period.It promotes immune function recovery,reduces the inflammatory response,and decreases the risk of adverse effects.These beneficial effects make it worth investigating and promoting their use in ap-propriate patient populations.However,further validation via high-quality studies with long intervention time and extended follow-up periods is required.
基金supported by National Natural Science Foundation of China(U22 A20515)National High-Level Talents Special Support Program of China(2021-WR-01)Agricultural Science and Technology Innovation Program(ASTIPIAS07).
文摘Background Colitis caused by bacterial infection is a major global health challenge.Unfortunately,current treatment options are limited.We previously disclosed that L.reuteri SXDT-32 was enriched in the feces of an ancient diarrhearesistant pig breed(Mashen pig)in China over 2500 years old.As diarrhea is often closely associated with intestinal inflammation,L.reuteri SXDT-32 was identified as a potential beneficial bacterium to prevent intestinal inflammation.However,the precise mechanisms involved remained unclear.Results Our tests showed that L.reuteri SXDT-32 alleviated colonic damage induced by pathogenic E.coli SKLAN202302 in weaned pigs by enhancing barrier integrity and inhibiting inflammation.The transcriptomics revealed that L.reuteri SXDT-32 protected against inflammatory injury by inhibiting the PI3K-AKT signaling pathway.Metabolite analysis indicated that the content of shikimic acid(SA)was substantially elevated in the colonic mucosa of L.reuteri SXDT-32-fed piglets(P<0.05).In addition,Liquid Chromatography-Mass Spectrometer(LC-MS)analysis showed significant increases in SA content in both the colonic chyme of L.reuteri SXDT-32-fed piglets and the supernatant of in vitro grown cultures of L.reuteri SXDT-32(P<0.05).Polymerase chain reaction(PCR)analysis identified gene aroE from L.reuteri SXDT-32,which is a key gene directly linked to SA synthesis,and elevated shikimate dehydrogenase(SD,encoded by aroE)was also detected in both L.reuteri SXDT-32 and the colonic mucosa of piglets fed L.reuteri SXDT-32(P<0.01).In vitro Caco-2 cell experiments demonstrated that SA,L.reuteri SXDT-32,and the supernatant from in vitro grown cultures of L.reuteri SXDT-32 exhibited comparable inhibitory effects on the PI3K-Akt pathway to those of the PI3K inhibitor LY294002.Conclusions L.reuteri SXDT-32 alleviated intestinal inflammation in piglets by producing SA that inhibits the PI3K-Akt pathway.This study provides an innovative approach for the treatment and prevention of colitis caused by bacterial infection.
基金financially supported by Beijing Natural Science Foundation[7252202,25JL008,China]from Beijing Natural Science Foundation CommitteeThis work was also supported by CAMS Innovation Fund for Medical Sciences[2021-I2M-1-029,2023-12M-2-006,China]and[2021-I2M-1-028,China]from Chinese Academy of Medical Science&Peking Union Medical College(CAMS&PUMC)+1 种基金National Natural Science Foundation of China[81703536 and 22278443,China]from Natural Science Foundation CommitteeInternational Cooperation Project of Qinghai Province[2020-HZ-803,China]from Science and Technology Department of Qinghai Province.
文摘Objectives:Colorectal cancer(CRC)is one of the most common cancers all over the world.The progression of CRC is associated with inflammation and disruptions in intestinal flora.3-O-Acetyl-11-keto-β-boswellic acid(AKBA)has been noted for its potent anti-inflammatory properties.However,the effect of AKBA on colon cancer caused by inflammation and its mechanism are not unclear.The study is to explore the effect of AKBA on CRC and its mechanism.Materials and Methods:Cell proliferation,(5-ethynyl-2′-deoxyuridine,EdU)-DNA synthesis assay and colony formation were used to assess the effect of AKBA on the proliferation of CRC cells.Flow cytometry was employed to analyze the cell cycle and apoptosis rate of cells treated with AKBA.RNA sequencing was done to explore the underlying mechanisms of AKBA.Western blot was used to assess the expression of key proteins in the nuclear factor kappa-B(NF-κB)signaling pathway after the treatment of AKBA.Real-time quantitative PCR(RT-qPCR),enzyme-linked immunosorbent assay(ELISA),and Meso Scale Discovery(MSD)assays were employed to check the anti-inflammation effects of AKBA on Lipopolysaccharide(LPS)-induced RAW264.7 cells and LPS-induced mouse model.Additionally,the Azoxymethane/Dextran sulfate sodium(AOM/DSS)-induced colitis-associated CRC model was used to evaluate the anti-CRC effect of AKBA.Gut microbiota profiling of fecal samples from CRC mice,both with and without AKBA treatment,was conducted through metagenomic sequencing analysis.Results:Our results showed that AKBA reduced the proliferation of HCT116 and SW620 cells,increased apoptosis of cells,and arrested the cell cycle at the G2/M phase.Results from RNA-seq showed that AKBA inhibited CRC by inhibiting the NF-κB signaling pathway and reducing cellular inflammation.Furthermore,AKBA reduced the levels of inflammatory cytokines,including tumor necrosis factor-α(TNF-α),Interferon-γ(IFN-γ),Interleukin-IL-12p70(IL-12p70),Interleukin-1β(IL-1β),and tumor necrosis factor-α(TNF-α)in both the spleen and serum of LPS-induced acute inflammation mice.Additionally,AKBA inhibited the development of AOM/DSS-induced colitis-associated colon cancer in mice and positively influenced gut microbiota.Conclusion:This study highlights the inhibitory effect of AKBA on colitis-associated CRC and reveals a novel aspect of its role in the remodeling of gut microbiota.These findings suggest that AKBA may be used as a potential therapeutic agent for CRC.
文摘BACKGROUND Gastric cancer(GC)is a type of cancer which causes high cancer-related mortality.Surgical operation and systematic chemical therapies are primary choices for the treatment of GC patients with advanced stages,however,the 5-year overall survival is only around 30%.AIM To investigate the role of mesenchymal stem cell(MSC)-derived long non-coding RNAs(lncRNA)NKILA in fatty acid oxidation and chemoresistance in GC cells,mediated through the miR-485-5p/STAT3 pathway.METHODS GC cell lines(AGS and MKN45)were co-cultured with human bone marrowderived MSCs were cultured.The MSC identity was confirmed by flow cytometry(CD73,CD90,CD105>95%positive,CD34,CD45 negative).Co-culture of GC cells and MSCs was performed in Transwell plates,where MSCs were placed in the upper chamber and GC cells in the lower chamber for 72 hours.For transfections,pcDNA-NKILA vectors,shSTAT3,and miR-485-5p mimics were utilized.Colony formation,apoptosis assays(Annexin V/PI staining),sphere formation,and flow cytometry were performed to evaluate cell proliferation,stemness,and chemoresistance.qPCR was used to analyze gene expression(Sox2,Oct4,CD133,LIN28,NKILA),and Western blotting assessed protein levels of stemness markers.Luciferase reporter assays were conducted to confirm miR-485-5p/STAT3 interactions,and biotin-labeled RNA pulldown was used to assess RNA-protein binding.Fatty acid oxidation was evaluated using a CPT1 activity assay andβ-oxidation rate detection.ATP levels were measured to assess the energetic status of GC cells.Clinical GC tissue samples were collected from patients at our hospital for validation.RESULTS MSCs were found to enhance the stemness and chemoresistance of GC cells.Co-culturing MKN45 and AGS cells with MSCs significantly increased sphere-forming ability and the expression of key cancer stem cell markers(SOX2,Oct4,LIN28,CD133),indicating that MSCs promote stem-like properties.Flow cytometry confirmed an enrichment of CD44+and CD133+subpopulations in MSC-treated GC cells.Additionally,MSC co-culture reduced chemotherapy-induced apoptosis and enhanced cell proliferation,suggesting a protective role in chemotherapy resistance.MSC-derived lncRNA NKILA further promoted stemness and chemoresistance,enhancing expression of stem cell markers and protecting cells from oxaliplatin and 5-FU-induced apoptosis.MSC co-culture also induced fatty acid oxidation in GC cells,as shown by increased CPT1 activity,β-oxidation rates,and ATP levels.NKILA mediated these effects by upregulating STAT3,which was confirmed to regulate fatty acid oxidation and chemoresistance.NKILA’s interaction with miR-485-5p further promoted STAT3 expression and fatty acid oxidation,reinforcing its role in maintaining stemness and enhancing chemoresistance.CONCLUSION MSCs enhance the stemness and chemoresistance of GC cells by secreting lncRNA NKILA,which promotes fatty acid oxidation through STAT3 activation.NKILA modulates the miR-485-5p/STAT3 axis,thereby increasing energy metabolism and supporting cancer stem cell properties.Targeting NKILA or the miR-485-5p/STAT3 pathway offers potential therapeutic strategies to overcome chemoresistance in GC.
基金Supported by the Natural Science Foundation of Jiangxi Province,No.20242BAB25489National Natural Science Foundation of China,No.82260211 and No.81460092+1 种基金Key Research and Development Project in Jiangxi Province,No.20203BBG73058Chinese Medicine Science and Technology Project in Jiangxi Province,No.2020A0166。
文摘BACKGROUND Diabetic retinopathy(DR)is the leading cause of vision loss in patients with diabetes.The vascular endothelial growth factor(VEGF)pathway plays a critical role in the pathogenesis of DR,and ranibizumab,an anti-VEGF agent,has shown promise in its treatment.Signal transducer and activator of transcription 3(STAT3)is involved in inflammatory processes and cellular signaling,while glial fibrillary acidic protein(GFAP)is a marker of glial cell activation,both contributing to retinal damage in DR.However,the mechanisms by which ranibizumab affect early-stage DR through the VEGF/STAT3/GFAP pathway are not fully understood.AIM To investigate the role of ranibizumab in early DR via the VEGF/STAT3/GFAP pathway.METHODS Adult retinal pigment epithelial 19(ARPE-19)cells and human retinal microvascular endothelial cells(HRMECs)were cultured under high-glucose conditions to simulate a diabetic environment.The effects of ranibizumab on cytokine mRNA and protein expression were analyzed by quantitative polymerase chain reaction and Western blot analysis.A diabetic rat model was induced with streptozotocin(60 mg/kg).Retinal changes,including retinal ganglion cell(RGC)apoptosis,vascular alterations,and cytokine expression,were evaluated using fundus fluorescein angiography,hematoxylin and eosin and periodic acid Schiff staining,immunofluorescence,confocal imaging,and Western blot analysis.RESULTS High-glucose conditions significantly increased the mRNA and protein levels of VEGF,STAT3,GFAP,and other cytokines in ARPE-19 and HRMECs.However,these levels were partially suppressed by ranibizumab.RGC apoptosis,vascular leakage,and elevated cytokine expression were observed during early-stage DR in diabetic rats.Ranibizumab treatment in diabetic rats reduced cytokine expression,restored RGCs,and repaired vascular networks.CONCLUSION Intravitreal ranibizumab modulates the VEGF/STAT3/GFAP pathway,suppresses cytokine expression,and promotes retinal repair,effectively delaying or preventing early DR progression.
基金Supported by The National Natural Science Foundation of China,No.82103356.
文摘BACKGROUND Improving our understanding of whether increased dietary intake ofω-3 polyunsaturated fatty acids(PUFAs)is beneficial for increasing skeletal muscle mass in patients with metabolic dysfunction-associated fatty liver disease(MAFLD)could provide an important clinical evidence base for the development of relevant nutritional guidelines.AIM To investigate the effect of total dietaryω-3 PUFAs and their subtypes on skeletal muscle mass in MAFLD.METHODS This cross-sectional study involved 2316 participants from four National Health and Nutrition Examination Survey cycles between 2011 and 2018.Dietary intake ofω-3 PUFAs was collected through 24-hour dietary recall interviews.Appendicular skeletal muscle mass index(ASMI)was calculated by dividing ASM in kilograms by height squared.RESULTS The multiple linear regression model showed significant relationships for dietary intake of totalω-3 PUFAs with higher ASMI(β:0.06,95%CI:0.01-0.11)in MAFLD patients.Dietary a-linolenic acid(ALA)(β:0.06,95%CI:0.01-0.12),docosapentaenoic acid(β:1.28,95%CI:0.01-2.54),and docosahexaenoic acid(DHA)(β:0.19,95%CI:0.01-0.37)were significantly associated with higher ASMI,while intake of stearidonic acid and eicosapentaenoic acid did not improve ASMI.In patients with high probability of liver fibrosis,dietary intake of ALA was associated with higher ASMI(β:0.11,95%CI:0.03-0.18).Stratified analysis found that DHA was associated with higher ASMI in patients with obesity and higher metabolic risk.CONCLUSION Increasing dietary intake ofω-3 PUFAs improved skeletal muscle health in patients with MAFLD.Patient with obesity and higher metabolic risk were more likely to benefit from intake of DHA.
基金the National Key Research and Development Program of China(Nos.2023YFD1700303,2022YFD17800)National Natural Science Foundation of China(Nos.21878088,21476077)for financial support。
文摘Triflumezopyrim(TFM)is a novel mesoionic pyrido[1,2-α]pyrimidinones insecticide,which acts on nicotinic acetylcholine receptors(n ACh Rs)and has no cross-resistance with other insecticides.Herein,we firstly developed a new continuous flow approach to synthesis 2-[3-(trifluoromethyl)phenyl]malonic acid,a key intermate of TFM,coupling with esterification,condensation,and hydrolysis.All three-step reactions were optimized and transformed into a continuous synthesis mode by three micro reaction units.Compared with the batch mode,the total reaction time and overall separation yield were improved from more than 12 h and 60%to 18 min and 73.38%,respectively.The solvent consumption and waste emission were significantly reduced,which also provides an eco-friendly and efficient potential tool for the development and production of mesoionic pyrido[1,2-α]pyrimidinones insecticide.
基金supported by the National Key R&D Program of China(Nos.2023YFC3707200 and 2022YFC3704400)the National Natural Science Foundation of China(Nos.52200136,22402220,and 52225004)Hangzhou Qianjiang Distinguished Experts Project.
文摘Ammonia Selective Catalytic Reduction(NHs-SCR)technology has been employed to eliminate NO_(x) from diesel engine exhaust,with Cu-SSZ-13 serving as the commercial catalyst.The greenhouse gas N_(2)O is produced as a byproduct when using Cu-SSZ-13 as the NH_(3)-SCR catalyst.To achieve synergistic control of pollutants and greenhouse gases in diesel engine exhaust,rational design of Cu-SSZ-13 catalysts is required.In this study,the effect of Brønsted acid sites in Cu-SSZ-13 catalysts on the formation of N_(2)O was investigated.Mild thermal treatmentwas innovatively employed to prepare Cu-SSZ-13 catalysts with different amounts of Brønsted acid sites.EPR,H_(2)-TPR,NH_(3)-TPD,NMR were utilized to determine that the Brønsted acid sites were modified while the Cu species remained unchanged.Thereby an accurate assessment of the influence of Brønsted acid sites on N_(2)O formation could be achieved.Our results showed that Cu-SSZ-13 with more Brønsted acid sites produced less N_(2)O during the NH_(3)-SCR reaction.In the low-temperature region,the presence of framework acid sites facilitates the decomposition of the NH_(4)NO_(3)assisted by NO to form N_(2)and H_(2)O,reducing the formation of N_(2)O.In the high-temperature region,the Brønsted acid sites promote the decomposition of NH_(2)NO into N_(2)and H_(2)O.Meanwhile,the N_(2)O-SCR reaction can also be promoted by Brønsted acid sites,thereby decreasing N_(2)O emissions.This study suggests that in the future design and synthesis of Cu-SSZ-13 zeolites,attention should be paid to creating more Brønsted acid sites in Cu-SSZ-13 to reduce N_(2)O emissions.
