[Objectives]To study the anti-inflammatory effect of Laggerae Alatae Herba extract and its mechanism.[Methods]Inflammation models of xylene-induced ear edema in mice,acetic acid-induced increased permeability of abdom...[Objectives]To study the anti-inflammatory effect of Laggerae Alatae Herba extract and its mechanism.[Methods]Inflammation models of xylene-induced ear edema in mice,acetic acid-induced increased permeability of abdominal capillaries in mice,and carrageenan-induced paw edema in mice were established;xylene-induced ear swelling model in bilateral adrenalectomized mice was established.The levels of MDA,NO and SOD in inflammatory tissues of paw were measured.[Results]Compared with the model group,the high and medium dose groups of Laggerae Alatae Herba extract had significant inhibitory effect on xylene-induced ear edema in mice,except for the low dose group(P>0.05);Laggerae Alatae Herba extract inhibited the increase of celiac capillary permeability induced by acetic acid and paw edema induced by carrageenan in mice.Compared with the model group,in the mice model with bilateral adrenal glands removed,the high and medium dose groups of Laggerae Alatae Herba extract could significantly inhibit the xylene induced ear swelling of the mice.The high and medium dose groups of Laggerae Alatae Herba extract could significantly decrease the levels of MDA and NO,and significantly increase the level of SOD in the paw tissue.[Conclusions]The Laggerae Alatae Herba extracts have anti-inflammatory activity,and the anti-inflammatory effect of the extracts does not depend on the hypothalamic-pituitary-adrenal axis(HPAA)system.In addition,the anti-inflammatory mechanism of Laggerae Alatae Herba extract is related to the decrease of MDA and NO and the increase of SOD.展开更多
[Objectives]Taking chlorogenic acid as index component,TLC and content determination method of Laggerae Alatae Herba were established.[Methods]TLC identification used silica gel G thin-layer plate,and butyl acetate∶f...[Objectives]Taking chlorogenic acid as index component,TLC and content determination method of Laggerae Alatae Herba were established.[Methods]TLC identification used silica gel G thin-layer plate,and butyl acetate∶formic acid∶water(7∶2.5∶2.5)was taken as developing agent,and it was inspected under ultraviolet lamp(365 nm).The content was determined by chromatographic column Inertsil ODS-3 C_(18)(4.60 mm×250 mm,5μm).Mobile phase:methanol-0.1%phosphoric acid(28∶72);detection wavelength:329 nm;flow speed:1.0 mL/min;column temperature:25℃;injection volume:10μL.[Results]Chlorogenic acid can be detected by TLC,with clear spots and good specificity.When injection volume of chlorogenic acid was between 0.099 and 0.990μg(R^(2)=0.9999),there was good linear relationship.In low,medium and high sample adding groups of Laggerae Alatae Herba,average recovery rates of chlorogenic acids were 98.80%(RSD=2.09%),98.24%(RSD=1.96%)and 99.65%(RSD=2.15%).[Conclusions]The method could effectively identify medicinal material Laggerae Alatae Herba,and accurately measure the content of chlorogenic acid in Laggerae Alatae Herba,thereby providing a scientific basis for developing and using medicinal resources of Laggerae Alatae Herba.展开更多
From the aerial part of Laggera alata, a novel eremophilanoid (1) as well as two new eudesmanoids (2-3) were isolated. Their structures were elucidated by 2D-NMR technique and X-ray diffraction studies. The cytotox...From the aerial part of Laggera alata, a novel eremophilanoid (1) as well as two new eudesmanoids (2-3) were isolated. Their structures were elucidated by 2D-NMR technique and X-ray diffraction studies. The cytotoxic activities of these sesquiterpenes were also investigated.展开更多
[Objectives] To establish a method for determining the content of Laggera alata( D. Don) Sch. Bip. Ex Oliv. using caffeic acid the target component,and to compare the content of caffeic acid in the medicinal materials...[Objectives] To establish a method for determining the content of Laggera alata( D. Don) Sch. Bip. Ex Oliv. using caffeic acid the target component,and to compare the content of caffeic acid in the medicinal materials of L. alata in different production areas of Guangxi.[Methods]The content was determined by Inertsil~ODS-3 chromatographic column C_(18)( 4. 60 mm × 250 mm,5 μm,mobile phase: acetonitrile-0. 1% phosphoric acid( 22∶ 78),detection wavelength: 320 nm,flow rate: 1. 0 m L/min,column temperature: 30℃,and injection volume: 10 μL. [Results] The caffeic acid showed a good linear relationship in the range of injection volume of 0. 025 92-0. 259 2 μg( R =0. 999 5). The average recovery rate was 98. 33%( RSD = 1. 85%). L. alata in different production areas of Guangxi contained the caffeic acid,and there was a great difference in the caffeic acid. L. alata in Baise had the highest content of caffeic acid,while that in Guilin had the lowest content of caffeic acid. [Conclusions]This method can accurately determine the content of caffeic acid and is expected provide a scientific basis for the development and utilization of herbal medicine L. alata.展开更多
[Objectives]This paper aims to establish thin-layer identification and content determination method for Laggera alata(D.Don)Sch.Bip.ex Oliv.with chlorogenic acid as the index component and compare the content of chlor...[Objectives]This paper aims to establish thin-layer identification and content determination method for Laggera alata(D.Don)Sch.Bip.ex Oliv.with chlorogenic acid as the index component and compare the content of chlorogenic acid in L.alata from different places in Guangxi.[Methods]Silica gel GF254 thin-layer plate was used for identification under an ultraviolet lamp(365 nm),with butyl acetate-formic acid-water(V∶V∶V=7∶2.5∶2.5)as a developing agent.The content of chlorogenic acid was determined under the following chromatographic conditions:column,Inertsil ODS-3 C18 column(4.60 mm×250 mm,5μm);mobile phase,methanol-0.1%phosphoric acid(28∶72);detection wavelength,329 nm;flow rate,1.0 mL/min;column temperature,25℃;and injection volume,10μL.[Results]Chlorogenic acid can be detected by thin layer chromatography with clear spot and good specificity.Chlorogenic acid showed a good linear relationship in the injection amount range of 0.099-0.99μg(R^(2)=0.9999).The content of chlorogenic acid in L.alata varied greatly among the 10 different producing areas in Guangxi.L.alata produced in Dee Township,Longlin,Baise,Guangxi showed the highest chlorogenic acid content,and that produced in Shangsi County and Pingle County showed the lowest chlorogenic acid content.[Conclusions]This method can effectively identify L.alata and accurately determine the content of chlorogenic acid,thereby providing a scientific basis for the development and utilization of L.alata resources.展开更多
[Objectives]To establish a method for quality analysis of Laggera alata.[Methods]The water content,total ash and alcohol-soluble extract of Laggera alata were determined according to the method of 2015 edition of Chin...[Objectives]To establish a method for quality analysis of Laggera alata.[Methods]The water content,total ash and alcohol-soluble extract of Laggera alata were determined according to the method of 2015 edition of Chinese Pharmacopoeia.[Results]Ten batches of Laggera alata from different producing areas and different collection time in Guangxi had the same plant morphology and medicinal properties.The experimental results were as follows:the water content was 5.19%-10.86%;the total ash content was 5.91%-10.74%;the acid-insoluble ash content was 0.44%-0.92%;the extract content was 14.64%-19.95%.[Conclusions]The experimental results can provide scientific basis for the development and utilization of Laggera alata and the establishment of its quality standard.展开更多
[Objectives]This study aimed to investigate the intervention effects of ethanol extract of Laggera alata(D.Don)Sch.Bip.ex Oliv on cirrhotic rats with ascites.[Methods]A total of 100 male SD rats of SPF grade were used...[Objectives]This study aimed to investigate the intervention effects of ethanol extract of Laggera alata(D.Don)Sch.Bip.ex Oliv on cirrhotic rats with ascites.[Methods]A total of 100 male SD rats of SPF grade were used.Rat models of cirrhosis and ascites were established.After the last administration,the amount of peritoneal fluid was measured,and the blood of each rat tested was collected for determination of serum AST,ALT and ALB levels,serum K+concentration and plasma Ald level.[Results]In ascitic cirrhotic rats,the livers showed obvious enlargement,the surface of the livers was uneven,and nodules were visible.Compared with the blank group,the amount of peritoneal fluid in the model group increased significantly(P<0.01);and compared with the model group,the amounts of peritoneal fluid in the high and medium-dose ethanol extract groups reduced significantly(P<0.01).Compared with the blank group,the serum ALT and AST levels in the model group increased significantly(P<0.01);and compared with the model group,the serum ALT and AST levels in the high-dose ethanol extract group decreased significantly(P<0.05).Compared with the blank group,the serum K+concentration in the positive group reduced(P<0.05);no significant difference was found in serum K+concentration between the ethanol extract administration groups and the blank group(P>0.05).Compared with the blank group,the plasma Ald levels in the high-dose ethanol extract group and the positive group reduced(P<0.05);and there was no significant difference in serum K+concentration between the rest groups and the blank group(P>0.05).[Conclusions]In the ethanol extract administration groups,the amounts of peritoneal fluid significantly reduced,the serum ALT and AST reduced,and the liver functions improved to a certain extent,indicating that the ethanol extract of L.alata(D.Don)Sch.Bip.ex Oliv has a better correction effect on electrolyte disturbances in cirrhotic rats with ascites.展开更多
The purpose of this study was to investigate the effect of Laggera alata flavonen （LAF） on the inhibit- ing effect of human ovarian cancer HO-8910 cells proliferation and its possible mechanism in vitro. Methods： H...The purpose of this study was to investigate the effect of Laggera alata flavonen （LAF） on the inhibit- ing effect of human ovarian cancer HO-8910 cells proliferation and its possible mechanism in vitro. Methods： Human ovarian cancer HO-8910 cells were cultured in vitro. Inhibitory effect of LAF on the viability of HO-8910 cells was evaluated by the MTT assay. Apoptotic effect of different concentrations of LAF on HO-8910 cells was assessed by AO/EB staining and FCM with propidium iodide （PI） staining. Expression of proteins related to apoptosis was analyzed by Western blot. Results： LAF significantly inhibited the viability of HO-8910 cells proliferation in a dose-dependent and time-dependent manner, there were statistical significance compared with NS group （P 〈 0.05）, and the ICso was 4.28 pg/mL for 48 h. The cells treated with LAF showed typical morphological change and apoptotic rate increased by FCM in a dose-dependent, and there was notable dif- ference compared with NS group （P 〈 0.05）. Western blot showed that expression of Fas, caspase-8, tBid and Cyto-c proteins were up-regulated after treatment with LAF for 48 h in a concentration dependent. Conclusion： LAF could inhibit HO-8910 cells proliferation and induce apoptosis, which may be through the pathway of death receptor in vitro.展开更多
基金Supported by State Administration of Traditional Chinese Medicine High-level Key Discipline Construction Project of Traditional Chinese Medicine-Ethnic Minority Pharmacy (Zhuang Pharmacy) (zyyzdxk-2023165)Cultivation Project of Guangxi International Zhuang Medicine Hospital (2023GZYJKT008)+6 种基金Youth Fund of Natural Science Foundation of Guangxi (2024GXNSFBA010302)Young Talent Cultivation Program of Guangxi International Zhuang Medicine Hospital (2022001)Key R&D Project of Guangxi Science and Technology Department (Guike AB21196057)Guangxi Traditional Chinese Medicine Interdisciplinary Innovation Team Project (GZKJ2309)Funding Project of High-level Talent Cultivation and Innovation Team of Guangxi University of Chinese Medicine (2022A008)The Third Batch of"Qihuang Project"High-Level Talent Team Training Project of Guangxi University of Chinese Medicine (202414)Three-year Action Plan for the Construction of High-level Talents Team of Guangxi International Zhuang Medicine Hospital in 2023 (GZCX20231203).
文摘[Objectives]To study the anti-inflammatory effect of Laggerae Alatae Herba extract and its mechanism.[Methods]Inflammation models of xylene-induced ear edema in mice,acetic acid-induced increased permeability of abdominal capillaries in mice,and carrageenan-induced paw edema in mice were established;xylene-induced ear swelling model in bilateral adrenalectomized mice was established.The levels of MDA,NO and SOD in inflammatory tissues of paw were measured.[Results]Compared with the model group,the high and medium dose groups of Laggerae Alatae Herba extract had significant inhibitory effect on xylene-induced ear edema in mice,except for the low dose group(P>0.05);Laggerae Alatae Herba extract inhibited the increase of celiac capillary permeability induced by acetic acid and paw edema induced by carrageenan in mice.Compared with the model group,in the mice model with bilateral adrenal glands removed,the high and medium dose groups of Laggerae Alatae Herba extract could significantly inhibit the xylene induced ear swelling of the mice.The high and medium dose groups of Laggerae Alatae Herba extract could significantly decrease the levels of MDA and NO,and significantly increase the level of SOD in the paw tissue.[Conclusions]The Laggerae Alatae Herba extracts have anti-inflammatory activity,and the anti-inflammatory effect of the extracts does not depend on the hypothalamic-pituitary-adrenal axis(HPAA)system.In addition,the anti-inflammatory mechanism of Laggerae Alatae Herba extract is related to the decrease of MDA and NO and the increase of SOD.
基金Supported by Key R&D Projects of Guangxi Science and Technology Department (GUIKE AB21196057)Basic Scientific Research Ability Improvement Project of Young and Middle-aged Teachers in Guangxi Universities and Colleges in 2019 (2019KY0341)+1 种基金Open Project of Guangxi Zhuang Yao Medicine Key Laboratory (GXZYKF2020A-08)Zhuang Pharmacy,a Key Discipline of Traditional Chinese Medicine (Ethnic Pharmacy) in the"12^th Five-year" Plan of the State Administration of Traditional Chinese Medicine
文摘[Objectives]Taking chlorogenic acid as index component,TLC and content determination method of Laggerae Alatae Herba were established.[Methods]TLC identification used silica gel G thin-layer plate,and butyl acetate∶formic acid∶water(7∶2.5∶2.5)was taken as developing agent,and it was inspected under ultraviolet lamp(365 nm).The content was determined by chromatographic column Inertsil ODS-3 C_(18)(4.60 mm×250 mm,5μm).Mobile phase:methanol-0.1%phosphoric acid(28∶72);detection wavelength:329 nm;flow speed:1.0 mL/min;column temperature:25℃;injection volume:10μL.[Results]Chlorogenic acid can be detected by TLC,with clear spots and good specificity.When injection volume of chlorogenic acid was between 0.099 and 0.990μg(R^(2)=0.9999),there was good linear relationship.In low,medium and high sample adding groups of Laggerae Alatae Herba,average recovery rates of chlorogenic acids were 98.80%(RSD=2.09%),98.24%(RSD=1.96%)and 99.65%(RSD=2.15%).[Conclusions]The method could effectively identify medicinal material Laggerae Alatae Herba,and accurately measure the content of chlorogenic acid in Laggerae Alatae Herba,thereby providing a scientific basis for developing and using medicinal resources of Laggerae Alatae Herba.
基金This work was financed in part by the Life Sciences Special Fund of Chinese Academy of Sciences supported by the Ministry of Finance (STZ-00-24) the Yunnan Province Foundation of Applied Basic Research (2000C0072M)+1 种基金 Chine-France PRA BT01-02 and the
文摘From the aerial part of Laggera alata, a novel eremophilanoid (1) as well as two new eudesmanoids (2-3) were isolated. Their structures were elucidated by 2D-NMR technique and X-ray diffraction studies. The cytotoxic activities of these sesquiterpenes were also investigated.
基金Supported by Project of National Natural Science Foundation(81660701&81260673)Project of Guangxi Graduate Education Innovation(YJS201625)+2 种基金Natural Science Foundation Project of Guangxi(2016GXNSFAA380148&2014GXNSFAA118208)Program of Key Laboratory for Purification and Quality Analysis of TCM Extraction in Guangxi Universities(Gui Jiao Ke Yan[2014]No.6)Laboratory of Chemistry and Quality Analysis in the Third Level Laboratory for Research of TCM(Zhuang)of State Administration of Traditional Chinese Medicine(Guo Zhong Yi Yao Fa[200]No.21)
文摘[Objectives] To establish a method for determining the content of Laggera alata( D. Don) Sch. Bip. Ex Oliv. using caffeic acid the target component,and to compare the content of caffeic acid in the medicinal materials of L. alata in different production areas of Guangxi.[Methods]The content was determined by Inertsil~ODS-3 chromatographic column C_(18)( 4. 60 mm × 250 mm,5 μm,mobile phase: acetonitrile-0. 1% phosphoric acid( 22∶ 78),detection wavelength: 320 nm,flow rate: 1. 0 m L/min,column temperature: 30℃,and injection volume: 10 μL. [Results] The caffeic acid showed a good linear relationship in the range of injection volume of 0. 025 92-0. 259 2 μg( R =0. 999 5). The average recovery rate was 98. 33%( RSD = 1. 85%). L. alata in different production areas of Guangxi contained the caffeic acid,and there was a great difference in the caffeic acid. L. alata in Baise had the highest content of caffeic acid,while that in Guilin had the lowest content of caffeic acid. [Conclusions]This method can accurately determine the content of caffeic acid and is expected provide a scientific basis for the development and utilization of herbal medicine L. alata.
基金Basic Research Ability Enhancement Project for Young and Middle-aged Teachers in Colleges and Universities of Guangxi in 2019(No.2019KY0341)National Traditional Chinese Medicine Special Technology Inheritance Talent Training Project 2016+1 种基金Open Project of Guangxi Zhuang Yao Pharmaceutical Engineering Technology Research Center(No.KJT1900105)Youth Foundation of Guangxi University of Chinese Medicine(No.2019QN036).
文摘[Objectives]This paper aims to establish thin-layer identification and content determination method for Laggera alata(D.Don)Sch.Bip.ex Oliv.with chlorogenic acid as the index component and compare the content of chlorogenic acid in L.alata from different places in Guangxi.[Methods]Silica gel GF254 thin-layer plate was used for identification under an ultraviolet lamp(365 nm),with butyl acetate-formic acid-water(V∶V∶V=7∶2.5∶2.5)as a developing agent.The content of chlorogenic acid was determined under the following chromatographic conditions:column,Inertsil ODS-3 C18 column(4.60 mm×250 mm,5μm);mobile phase,methanol-0.1%phosphoric acid(28∶72);detection wavelength,329 nm;flow rate,1.0 mL/min;column temperature,25℃;and injection volume,10μL.[Results]Chlorogenic acid can be detected by thin layer chromatography with clear spot and good specificity.Chlorogenic acid showed a good linear relationship in the injection amount range of 0.099-0.99μg(R^(2)=0.9999).The content of chlorogenic acid in L.alata varied greatly among the 10 different producing areas in Guangxi.L.alata produced in Dee Township,Longlin,Baise,Guangxi showed the highest chlorogenic acid content,and that produced in Shangsi County and Pingle County showed the lowest chlorogenic acid content.[Conclusions]This method can effectively identify L.alata and accurately determine the content of chlorogenic acid,thereby providing a scientific basis for the development and utilization of L.alata resources.
基金Project for Improving the Basic Scientific Research Ability of Young and Middle-aged Teachers in Colleges and Universities of Guangxi in 2019(2019KY0341)Key Research and Development Project of Guangxi Department of Science and Technology(AB19110003)+1 种基金2019 Youth Fund Project of Guangxi University of Chinese Medicine(2019QN036)Laboratory of Chemistry and Quality Analysis of Chinese(Zhuang)Medicine in the Third-level Scientific Research Laboratory of the State Administration of Traditional Chinese Medicine(Guo Zhong Yi Yao Fa 200921).
文摘[Objectives]To establish a method for quality analysis of Laggera alata.[Methods]The water content,total ash and alcohol-soluble extract of Laggera alata were determined according to the method of 2015 edition of Chinese Pharmacopoeia.[Results]Ten batches of Laggera alata from different producing areas and different collection time in Guangxi had the same plant morphology and medicinal properties.The experimental results were as follows:the water content was 5.19%-10.86%;the total ash content was 5.91%-10.74%;the acid-insoluble ash content was 0.44%-0.92%;the extract content was 14.64%-19.95%.[Conclusions]The experimental results can provide scientific basis for the development and utilization of Laggera alata and the establishment of its quality standard.
基金Guangxi Young and Middle-aged University Teachers'Scientific Research Ability Enhancement Project(No.2019KY0341)Foundation of Administration of Traditional Chinese Medicine of Guangxi Zhuang Autonomous Region(No.GZZC2019147)+2 种基金Youth Foundation of Guangxi University of Chinese Medicine(No.2019QN036)University-level Scientific Research Project of Youjiang Medical University for Nationalities(yy2018ky018)Scientific Research Laboratories of National Administration of Traditional Chinese Medicine(Level III):Chemistry and Quality Analysis Laboratory of Chinese(Zhuang)Medicine(Guo Zhong Yi Yao Fa 2009[21]).
文摘[Objectives]This study aimed to investigate the intervention effects of ethanol extract of Laggera alata(D.Don)Sch.Bip.ex Oliv on cirrhotic rats with ascites.[Methods]A total of 100 male SD rats of SPF grade were used.Rat models of cirrhosis and ascites were established.After the last administration,the amount of peritoneal fluid was measured,and the blood of each rat tested was collected for determination of serum AST,ALT and ALB levels,serum K+concentration and plasma Ald level.[Results]In ascitic cirrhotic rats,the livers showed obvious enlargement,the surface of the livers was uneven,and nodules were visible.Compared with the blank group,the amount of peritoneal fluid in the model group increased significantly(P<0.01);and compared with the model group,the amounts of peritoneal fluid in the high and medium-dose ethanol extract groups reduced significantly(P<0.01).Compared with the blank group,the serum ALT and AST levels in the model group increased significantly(P<0.01);and compared with the model group,the serum ALT and AST levels in the high-dose ethanol extract group decreased significantly(P<0.05).Compared with the blank group,the serum K+concentration in the positive group reduced(P<0.05);no significant difference was found in serum K+concentration between the ethanol extract administration groups and the blank group(P>0.05).Compared with the blank group,the plasma Ald levels in the high-dose ethanol extract group and the positive group reduced(P<0.05);and there was no significant difference in serum K+concentration between the rest groups and the blank group(P>0.05).[Conclusions]In the ethanol extract administration groups,the amounts of peritoneal fluid significantly reduced,the serum ALT and AST reduced,and the liver functions improved to a certain extent,indicating that the ethanol extract of L.alata(D.Don)Sch.Bip.ex Oliv has a better correction effect on electrolyte disturbances in cirrhotic rats with ascites.
文摘The purpose of this study was to investigate the effect of Laggera alata flavonen （LAF） on the inhibit- ing effect of human ovarian cancer HO-8910 cells proliferation and its possible mechanism in vitro. Methods： Human ovarian cancer HO-8910 cells were cultured in vitro. Inhibitory effect of LAF on the viability of HO-8910 cells was evaluated by the MTT assay. Apoptotic effect of different concentrations of LAF on HO-8910 cells was assessed by AO/EB staining and FCM with propidium iodide （PI） staining. Expression of proteins related to apoptosis was analyzed by Western blot. Results： LAF significantly inhibited the viability of HO-8910 cells proliferation in a dose-dependent and time-dependent manner, there were statistical significance compared with NS group （P 〈 0.05）, and the ICso was 4.28 pg/mL for 48 h. The cells treated with LAF showed typical morphological change and apoptotic rate increased by FCM in a dose-dependent, and there was notable dif- ference compared with NS group （P 〈 0.05）. Western blot showed that expression of Fas, caspase-8, tBid and Cyto-c proteins were up-regulated after treatment with LAF for 48 h in a concentration dependent. Conclusion： LAF could inhibit HO-8910 cells proliferation and induce apoptosis, which may be through the pathway of death receptor in vitro.
