Pectolinarigenin is a kind of flavonoid,which is an active ingredient in Eupatorium odoratum.Some studies have confirmed that pectolinarigenin has many biological activities,including anti-oxidation,anti-allergy,anti-...Pectolinarigenin is a kind of flavonoid,which is an active ingredient in Eupatorium odoratum.Some studies have confirmed that pectolinarigenin has many biological activities,including anti-oxidation,anti-allergy,anti-inflammation,anti-tumor and so on.In this paper,the biological activity and related mechanism of pectolinarigenin were summarized in order to provide theoretical basis and reference for the further development and utilization of pectolinarigenin.展开更多
Objective:To characterize the oxidative metabolic pathway(s)of pectolinarigenin(PEC)and reveal the effect of PEC oxidative metabolism on its biological activities including peroxisome proliferatoractivated receptors(P...Objective:To characterize the oxidative metabolic pathway(s)of pectolinarigenin(PEC)and reveal the effect of PEC oxidative metabolism on its biological activities including peroxisome proliferatoractivated receptors(PPAR)and nuclear factor erythroid 2-related factor 2(Nrf2)agonist effects,as well as the anti-oxidative and hepatoprotective activities.Methods:The oxidative metabolites of PEC were identified by liquid chromatography-time of flight-mass spectrometry(LC-TOF-MS/MS).The key enzymes involved in oxidative metabolism of PEC were assigned by P450 reaction phenotyping assays and enzymatic kinetics assays.Luciferase reporter assays and western blotting analysis were used to evaluate the Nrf2 and PPAR agonist effects of PEC and its oxidative metabolites.The intracellular levels of total reactive oxygen species(ROS),mitochondrial membrane potential(MMP),lactate dehydrogenase(LDH)and glutathione(GSH)in acetaminophen(APAP)-challenged hepatocytes were also tested.Results:PEC could be readily metabolized to form two O-demethylated metabolites including hispidulin(HIS,4′-O-demethylated PEC)and 6-O-demethylated PEC in human liver microsomes(HLM)in the presence of nicotinamide adenine dinucleotide phosphate(NADPH),while HIS was identified as the major oxidative metabolite of PEC.At least nine human cytochrome P450 enzymes(CYP)enzymes could catalyze PEC-4′-O-demethylation,while CYP1A2 and CYP2D6 showed the highest binding affinities and rapid metabolic clearance rates in the oxidative metabolism of PEC.Biological assays showed that PEC4′-O-demethylation slightly decreased the PPAR agonist effects of PEC,while HIS showed more potent Nrf2 agonist effect.Compared with PEC,HIS showed more efficacious hepatoprotective effect against APAP-induced hepatocyte injury,evidenced by more potent ability to reduce intracellular ROS and LDH levels,as well as more effective ability to elevate the intracellular levels of both MPP and GSH in APAP-challenged hepatocytes.Conclusion:CYPs catalyze PEC-4′-O-demethylation to generate a more active Nrf2 agonist(HIS),which shows more efficacious hepatoprotective effects against APAP-induced hepatocyte injury.展开更多
通过网络药理学和实验验证研究柳穿鱼黄素对宫颈癌HeLa和SiHa细胞增殖和迁移的影响。首先通过PharmMapper和SwissTargetPrediction数据库预测柳穿鱼黄素作用靶点,然后与来自GeneCards和OMIM等多个数据库的宫颈癌(CC)的疾病靶点进行交集...通过网络药理学和实验验证研究柳穿鱼黄素对宫颈癌HeLa和SiHa细胞增殖和迁移的影响。首先通过PharmMapper和SwissTargetPrediction数据库预测柳穿鱼黄素作用靶点,然后与来自GeneCards和OMIM等多个数据库的宫颈癌(CC)的疾病靶点进行交集分析,初步确定柳穿鱼黄素在CC治疗中的潜在作用靶点,进而构建靶蛋白相互作用网络,并依托基因本体论(GO)与京都基因和基因组百科全书(KEGG)筛选柳穿鱼黄素作用于CC的可能信号通路。以HeLa/SiHa细胞为模型,采用CCK-8、划痕、Transwell、集落形成和Western blotting等多种实验,研究柳穿鱼黄素对细胞增殖、迁移、克隆及JAK2/STAT3表达的作用。结果KEGG分析表明,柳穿鱼黄素作用于CC显著富集信号通路以Pathways in cancer、JAK2/STAT3通路、PI3K/Akt等为主。细胞实验结果显示,柳穿鱼黄素可显著抑制宫颈癌HeLa和SiHa细胞增殖和迁移的能力,且具有浓度依赖性(P<0.01),同时柳穿鱼黄素可降低宫颈癌HeLa和SiHa细胞p-JAK2和p-STAT3蛋白的表达水平(P<0.01)。柳穿鱼黄素可能通过调节JAK2/STAT3信号通路抑制宫颈癌细胞的增殖与迁移。展开更多
基金Heilongjiang Farms&Land Reclamation Administration Support Project for Key Seientifie Research(HKKYZD190705)Heilongjiang Bayi Agricultural University Support Program for"San Zong"(TDJH201905)Heilongjiang Touyan Innovation Team Program(2019HTY078).
文摘Pectolinarigenin is a kind of flavonoid,which is an active ingredient in Eupatorium odoratum.Some studies have confirmed that pectolinarigenin has many biological activities,including anti-oxidation,anti-allergy,anti-inflammation,anti-tumor and so on.In this paper,the biological activity and related mechanism of pectolinarigenin were summarized in order to provide theoretical basis and reference for the further development and utilization of pectolinarigenin.
基金supported by National Key Research and Development Program of China(No.2022YFC3502000)National Natural Science Foundation of China(No.U23A20516,82273897,82304616)+6 种基金Shanghai Science and Technology Innovation Action Plans(No.21S21900600)supported by Shanghai Science and Technology Committee,Shanghai Municipal Health Commission’s Traditional Chinese Medicine Research Project(No.2022CX005)Yangfan Program of Science and Technology Commission of Shanghai Municipality(No.23YF1447400)the Organizational Key Research and Development Program of Shanghai University of Traditional Chinese Medicine(No.2023YZZ02)Department of Science&Technology of Liaoning Province(No.2022JH2/20200056)New Quality Clinical Specialty Program of High-end Medical Disciplinary Construction in Shanghai Pudong New Area(No.2025-PWXZ-15)the Project for Inheritance,Innovation and Development of Traditional Chinese Medicine in Pudong New Area(No.YC-2023-0602)。
文摘Objective:To characterize the oxidative metabolic pathway(s)of pectolinarigenin(PEC)and reveal the effect of PEC oxidative metabolism on its biological activities including peroxisome proliferatoractivated receptors(PPAR)and nuclear factor erythroid 2-related factor 2(Nrf2)agonist effects,as well as the anti-oxidative and hepatoprotective activities.Methods:The oxidative metabolites of PEC were identified by liquid chromatography-time of flight-mass spectrometry(LC-TOF-MS/MS).The key enzymes involved in oxidative metabolism of PEC were assigned by P450 reaction phenotyping assays and enzymatic kinetics assays.Luciferase reporter assays and western blotting analysis were used to evaluate the Nrf2 and PPAR agonist effects of PEC and its oxidative metabolites.The intracellular levels of total reactive oxygen species(ROS),mitochondrial membrane potential(MMP),lactate dehydrogenase(LDH)and glutathione(GSH)in acetaminophen(APAP)-challenged hepatocytes were also tested.Results:PEC could be readily metabolized to form two O-demethylated metabolites including hispidulin(HIS,4′-O-demethylated PEC)and 6-O-demethylated PEC in human liver microsomes(HLM)in the presence of nicotinamide adenine dinucleotide phosphate(NADPH),while HIS was identified as the major oxidative metabolite of PEC.At least nine human cytochrome P450 enzymes(CYP)enzymes could catalyze PEC-4′-O-demethylation,while CYP1A2 and CYP2D6 showed the highest binding affinities and rapid metabolic clearance rates in the oxidative metabolism of PEC.Biological assays showed that PEC4′-O-demethylation slightly decreased the PPAR agonist effects of PEC,while HIS showed more potent Nrf2 agonist effect.Compared with PEC,HIS showed more efficacious hepatoprotective effect against APAP-induced hepatocyte injury,evidenced by more potent ability to reduce intracellular ROS and LDH levels,as well as more effective ability to elevate the intracellular levels of both MPP and GSH in APAP-challenged hepatocytes.Conclusion:CYPs catalyze PEC-4′-O-demethylation to generate a more active Nrf2 agonist(HIS),which shows more efficacious hepatoprotective effects against APAP-induced hepatocyte injury.
文摘通过网络药理学和实验验证研究柳穿鱼黄素对宫颈癌HeLa和SiHa细胞增殖和迁移的影响。首先通过PharmMapper和SwissTargetPrediction数据库预测柳穿鱼黄素作用靶点,然后与来自GeneCards和OMIM等多个数据库的宫颈癌(CC)的疾病靶点进行交集分析,初步确定柳穿鱼黄素在CC治疗中的潜在作用靶点,进而构建靶蛋白相互作用网络,并依托基因本体论(GO)与京都基因和基因组百科全书(KEGG)筛选柳穿鱼黄素作用于CC的可能信号通路。以HeLa/SiHa细胞为模型,采用CCK-8、划痕、Transwell、集落形成和Western blotting等多种实验,研究柳穿鱼黄素对细胞增殖、迁移、克隆及JAK2/STAT3表达的作用。结果KEGG分析表明,柳穿鱼黄素作用于CC显著富集信号通路以Pathways in cancer、JAK2/STAT3通路、PI3K/Akt等为主。细胞实验结果显示,柳穿鱼黄素可显著抑制宫颈癌HeLa和SiHa细胞增殖和迁移的能力,且具有浓度依赖性(P<0.01),同时柳穿鱼黄素可降低宫颈癌HeLa和SiHa细胞p-JAK2和p-STAT3蛋白的表达水平(P<0.01)。柳穿鱼黄素可能通过调节JAK2/STAT3信号通路抑制宫颈癌细胞的增殖与迁移。
