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Swertiamarin通过抑制肠上皮细胞细胞凋亡改善TNBS诱导的实验性结肠炎
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作者 刘硕 李静 吴兴旺 《南方医科大学学报》 CAS CSCD 北大核心 2024年第8期1545-1552,共8页
目的本研究旨在探讨Swertiamarin(STM)通过拮抗肠上皮细胞凋亡改善CD样结肠炎的作用和机制。方法体外建立TNF-α刺激的Caco-2细胞凋亡模型,分为3组:对照组(Con)、TNF-α刺激组(TNF-α)和STM干预组(STM),通过Tunel染色、免疫印迹、免疫... 目的本研究旨在探讨Swertiamarin(STM)通过拮抗肠上皮细胞凋亡改善CD样结肠炎的作用和机制。方法体外建立TNF-α刺激的Caco-2细胞凋亡模型,分为3组:对照组(Con)、TNF-α刺激组(TNF-α)和STM干预组(STM),通过Tunel染色、免疫印迹、免疫荧光和上皮电阻检测等方法,评估STM对细胞凋亡和屏障功能的影响。体内建立TNBS诱导的CD样结肠炎小鼠模型,分为3组:WT、TNBS和STM组,利用小鼠体质量变化、疾病活动指数评分、炎症评分和黏膜组织中炎症因子含量分析STM对结肠炎的作用;通过通透性、细菌移位率和紧密连接蛋白表达与定位观察STM对肠屏障功能的影响;使用Tunel染色和免疫印迹检测凋亡相关蛋白水平评估STM对上皮细胞凋亡的作用。体内外研究验证PI3K/AKT通路在STM抗肠上皮细胞凋亡中的调控作用。结果体外研究中TUNEL染色结果显示,STM显著得减少TUNEL着色的Caco-2细胞的比例(P<0.05);免疫印迹数据显示,STM组中cleavedcaspase3和Bax的表达低于TNF-α组(P<0.05),而Bcl2的水平则增高(P<0.05);肠屏障完整性和功能检测显示,STM恢复了TEER值(P<0.05)、促进了紧密连接蛋白(ZO1和claudin 1)的定位正常化和表达水平的上调(P<0.05),以及抑制了促炎因子(IL-6和CCL3)的表达(P<0.05)。体内研究显示STM能缓解结肠炎和肠屏障功能障碍,具体表现为体重下降、疾病活动指数(DAI)评分、炎症评分和促炎因子(IL-6和CCL3)释放以及肠屏障通透性、结肠TEER、细菌移位和紧密连接蛋白(ZO1和Claudin-1)定位与表达均得到了改善(P<0.05)。机制上,STM在体和体外均抑制了p-PI3K和p-AKT的表达(P<0.05),且PI3K/AKT通路的激活剂(740YP)阻遏了STM抗TNF-α诱导的Caco-2凋亡作用(P<0.05)。结论STM至少部分是通过抑制PI3K/AKT通路的激活,拮抗肠上皮细胞细胞的凋亡,进而改善肠屏障功能障碍和实验性结肠炎。 展开更多
关键词 克罗恩病 肠屏障 肠上皮细胞凋亡 SWERTIAMARIN PI3K/AKT通路
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Lomatogonium rotatum extract alleviates diabetes mellitus induced by a high-fat,high-sugar diet and streptozotocin in rats
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作者 Li-Li Dai Sung-Bo Cho +7 位作者 Hui-Fang Li Li-Sha A Xiao-Ping Ji Sirigunqiqige Pan Ming-Lan Bao Laxinamujila Bai Gen-Na Ba Ming-Hai Fu 《World Journal of Diabetes》 SCIE 2023年第6期846-861,共16页
BACKGROUND Lomatogonium rotatum(LR)is traditionally used in Mongolian folk medicine as a hypoglycemic agent,but its evidence-based pharmacological effects and mechanisms of action have not been fully elucidated.AIM To... BACKGROUND Lomatogonium rotatum(LR)is traditionally used in Mongolian folk medicine as a hypoglycemic agent,but its evidence-based pharmacological effects and mechanisms of action have not been fully elucidated.AIM To emphasize the hypoglycemic action mechanism of LR in a type 2 diabetic rat model and examine potential biomarkers to obtain mechanistic understanding regarding serum metabolite modifications.METHODS A high-fat,high-sugar diet and streptozotocin injection-induced type 2 diabetic rat model was established.The chemical composition of the LR was identified by high performance liquid chromatography.LR extract administrated as oral gavage at 0.5 g/kg,2.5 g/kg,and 5 g/kg for 4 wk.Anti-diabetic effects of LR extract were evaluated based on histopathological examination as well as the measurement of blood glucose,insulin,glucagon-like peptide 1(GLP-1),and lipid levels.Serum metabolites were analyzed using an untargeted metabolomics approach.RESULTS According to a chemical analysis,swertiamarin,sweroside,hesperetin,coumarin,1.7-dihydroxy-3,8-dimethoxyl xanthone,and 1-hydroxy-2,3,5 trimethoxanone are the principal active ingredients in LR.An anti-diabetic experiment revealed that the LR treatment significantly increased plasma insulin and GLP-1 levels while effectively lowering blood glucose,total cholesterol,triglycerides,low-density lipoprotein cholesterol,and oral glucose tolerance test compared to the model group.Furthermore,untargeted metabolomic analysis of serum samples detected 236 metabolites,among which 86 were differentially expressed between the model and the LR group.It was also found that LR considerably altered the levels of metabolites such as vitamin B6,mevalonate-5P,Dproline,L-lysine,and taurine,which are involved in the regulation of the vitamin B6 metabolic pathway,selenium amino acid metabolic pathway,pyrimidine metabolic pathway,and arginine and proline metabolic pathways.CONCLUSION These findings indicated that LR may have a hypoglycemic impact and that its role may be related to changes in the serum metabolites and to facilitate the release of insulin and GLP-1,which lower blood glucose and lipid profiles. 展开更多
关键词 Mongolian medicine Lomatogonium rotatum Type 2 diabetes Metabolomics SWERTIAMARIN STREPTOZOTOCIN
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Pharmacokinetics of nitrogen-containing metabolites R-gentiandiol and S-gentiandiol in rat plasma after oral administration of swertiamarin
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作者 LI Peng-yu CUI Fu-yan +6 位作者 HUANG Jin-yue TANG Meng JIANG Jia-xin MA Ying XIA Nian-tong YANG Bo WANG Zhi-gang 《Journal of Hainan Medical University》 CAS 2023年第6期22-27,共6页
Objective:A chiral resolution method for enantiomers of two chiral nitrogen-containing metabolites R-gentiandiol and S-gentiandiol of swertiamarin in plasma was developed,and the pharmacokinetics of the metabolites we... Objective:A chiral resolution method for enantiomers of two chiral nitrogen-containing metabolites R-gentiandiol and S-gentiandiol of swertiamarin in plasma was developed,and the pharmacokinetics of the metabolites were studied.Methods:The metabolites of swertiamarin in vivo were detected by LC-MS/MS using Astec CyclobondⅡCyclodextrin column(4.6 mm×100 mm,5μm),gradient elution with acetonitrile-water as mobile phase,and monitored by multiple reaction monitoring(MRM)method in positive mode.The ion pairs for quantitative analysis are R-gentiandiol(m/z 210.04→192.06),S-gentiandiol(m/z 210.04→192.06)and gentianone(m/z 192.02→162.08).Results:The linear correlation coefficients of the method developed were greater than 0.999,the precision was less than 7.00%,the recovery was 99.57%-102.65%,and the matrix effect was 90.94%-91.34%.The peak t_(max)of R-gentiandiol and S-gentiandiol in rat plasma after oral administration of swertiamarin were(1.63±0.23)h and(1.58±0.21)h,t_(1/2)was(6.23±0.52)h and(5.46±0.38)h,C_(max)was(86.79±20.81)ng/mL and(60.72±18.95)ng/mL,and the AUC_(0-24)were(1094.58±86.37))(ng·h)/mL and(724.67±58.38)(ng·h)/mL,respectively.Conclusion:The method was highly sensitive with good accuracy and precision,and it was successfully applied for chiral resolution and pharmacokinetics study of R-gentiandiol and S-gentiandiol in plasma.The method developed and experimental results will provide scientific basis for the study of pharmacodynamics and pharmacodynamic material basis of swertiamarin,and lay a foundation for clinical application and resource development of TCM monomer. 展开更多
关键词 SWERTIAMARIN METABOLITE R-gentiandiol S-gentiandiol PHARMACOKINETICS
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Förster resonance energy transfer reveals phillygenin and swertiamarin concurrently target AKT on different binding domains to increase the anti-inflammatory effect
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作者 Xiaoyao Ma Jinling Zhang +5 位作者 Ge Fang He Gao Jie Gao Li Fu Yuanyuan Hou Gang Bai 《Chinese Chemical Letters》 SCIE CAS CSCD 2024年第5期207-212,共6页
The clinical benefit of combination therapy is significant,but it is not easy to define the mechanism of complexity and diversity.Previous studies illustrate that phillygenin(Phi)binds in the allosteric inhibit pocket... The clinical benefit of combination therapy is significant,but it is not easy to define the mechanism of complexity and diversity.Previous studies illustrate that phillygenin(Phi)binds in the allosteric inhibit pocket of protein kinase B(AKT),and swertiamarin(Swe)acts on the pleckstrin homology(PH)domain of AKT.However,the combined synergistic effect of relieving the inflammatory response has yet to be elucidated.Based on high sensitivity,specificity and fast-responsibility fluorescent sensors,the Förster resonance energy transfer(FRET)technique offers a route to provide clear insights into physiological and pathological processes.In the study,molecular docking,the fluorescent probes of Phi and Swe for FRET were designed and synthesized.FRET analysis shown that Swe and Phi concurrently acted on the PH domain and allosterically inhibited pocket of AKT,respectively.The combination of Swe and Phi significantly increased the heat stability of AKT and decreased protease-induced degeneration.In lipopolysaccharides(LPS)-induced mice and cells,the combination arrested AKT activation,nuclear factor kappa-B(NF-κB)phosphorylation,and the expression of tumor necrosis factor-α(TNF-α),interleukin(IL)-6 and IL-8.In conclusion,FRET revealed Phi and Swe concurrently targeted AKT on different domains and the combination of Phi and Swe enhanced the anti-inflammatory effect. 展开更多
关键词 FRET SWERTIAMARIN Phillygenin AKT ANTI-INFLAMMATION Combinatorial drug
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Chemical fingerprint analysis of Gentianae Radix et Rhizoma by high-performance liquid chromatography 被引量:8
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作者 Baozhong Duan Jianyong Hu +2 位作者 Linfang Huang Xianying Yang Fuying Chen 《Acta Pharmaceutica Sinica B》 SCIE CAS 2012年第1期46-52,共7页
Gentianae Radix et Rhizoma(also called "Longdan" in Chinese)is commonly used for eliminating damp-heat and quenching the fire of liver and gall bladder in traditional Chinese medicine.In this study,a novel a... Gentianae Radix et Rhizoma(also called "Longdan" in Chinese)is commonly used for eliminating damp-heat and quenching the fire of liver and gall bladder in traditional Chinese medicine.In this study,a novel and reliable method using high-performance liquid chromatography(HPLC)was developed both for quantitative analysis of four bioactive compounds(loganic acid,swertiamarin,gentiopicroside and sweroside)and chemical fingerprint analysis of "Longdan".In quantitative analysis,four compounds showed good regressions(R^(2)>40.9987)within the test ranges and the recovery of the method was in the range 97.61-102.49%.In fingerprint analysis,ten characteristic peaks were selected to evaluate the similarities of the crude drugs,and the HPLC chromatograms of twenty samples from different regions of China showed similar patterns.The results demonstrated that the combination of the quantitative and chromatographic fingerprint analyses offered an efficient way to evaluate the quality consistency of Gentianae Radix et Rhizoma. 展开更多
关键词 Gentianae Radix et Rhizoma Loganic acid SWERTIAMARIN GENTIOPICROSIDE Sweroside HPLC Quantitative determination FINGERPRINT Quality control
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Anti-mutagenicity of Swertiamarin and Its Metabolite in Incubated System of Human Intestinal Flora 被引量:4
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作者 Cheng-wang Tian Ya-ting Cheng +1 位作者 Tie-jun Zhang Xiu-wei Yang 《Chinese Herbal Medicines》 CAS 2017年第1期92-95,共4页
Objective To study the biotransformation regulation and pharmacological effect of swertiamarin and its metabolite in incubated system of human intestinal flora. Methods Incubated system of human intestinal flora was u... Objective To study the biotransformation regulation and pharmacological effect of swertiamarin and its metabolite in incubated system of human intestinal flora. Methods Incubated system of human intestinal flora was utilized to research the intestinal metabolism of swertiamarin. Furthermore, mutagenic test and anti-mutagenic test were carried out to research the activity relationship of swertiamarin and its metabolite. Results Gentianine was found in the metabolites of swertiamarin. The pharmacological experiment indicated that swertiamarin and its metabolite both had good anti-mutagenic effect. Conclusion Swertiamarin is partly metabolized to gentianine after oral administration. They show similar anti-mutagenicity effects. 展开更多
关键词 anti-mutagenicity BIOTRANSFORMATION human intestinal flora SWERTIAMARIN
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