Suppr超能文献

酸枣仁皂苷B通过增加钙离子内流和激活内皮型一氧化氮合酶降低血管张力。

Jujuboside B Reduces Vascular Tension by Increasing Ca2+ Influx and Activating Endothelial Nitric Oxide Synthase.

作者信息

Zhao Yixiu, Zhang Xin, Li Jiannan, Bian Yu, Sheng Miaomiao, Liu Bin, Fu Zidong, Zhang Yan, Yang Baofeng

机构信息

Department of Pharmacology, Harbin Medical University, Harbin, Heilongjiang, PR China.

Key Laboratory of Cardiovascular Medicine Research (Harbin Medical University), Ministry of Education, Harbin, Heilongjiang, PR China.

出版信息

PLoS One. 2016 Feb 22;11(2):e0149386. doi: 10.1371/journal.pone.0149386. eCollection 2016.

Abstract

Jujuboside B has been reported to have protective effect on many cardiovascular diseases. However, the effects of Jujuboside B on vascular tension and endothelial function are unknown. The present study investigated the effects of Jujuboside B on reducing vascular tension, protecting endothelial function and the potential mechanisms. The tension of isolated rat thoracic aorta ring was measured by Wire myograph system. The concentration of nitric oxide (NO) and the activity of endothelial nitric oxide synthase (eNOS) in human aortic endothelial cells (HAECs) were determined by Griess reagent method and enzyme-linked immune sorbent assay. The protein levels of eNOS and p-eNOS at Serine-1177 were determined by western blot analysis. Intracellular Ca2+ concentration in HAECs was measured by laser confocal imaging microscopy. Results showed that Jujuboside B reduced the tension of rat thoracic aorta rings with intact endothelium in a dose-dependent manner. L-NAME, KN93, EGTA, SKF96365, iberiotoxin and glibenclamide significantly attenuated Jujuboside B-induced vasodilation in endothelium-intact tissues. In contrast, indometacin and 4-DAMP had no such effects. Jujuboside B also promoted NO generation and increased eNOS activity, which were attenuated by L-NAME, EGTA and SKF96365. Moreover, Jujuboside B increased intracellular Ca2+ concentration dose-dependently, which was inhibited by EGTA and SKF96365. Besides, Jujuboside B induced a rapid Ca2+ influx instantaneously after depleting intracellular Ca2+ store, which was significantly inhibited by SKF96365. In conclusion, this study preliminarily confirmed that Jujuboside B reduced vascular tension endothelium-dependently. The underlying mechanisms involved that Jujuboside B increased extracellular Ca2+ influx through endothelial transient receptor potential cation (TRPC) channels, phosphorylated eNOS and promoted NO generation in vascular endothelial cells. In addition, Jujuboside B-induced vasodilation involved endothelium-dependent hyperpolarizaiton through endothelial potassium channels. Jujuboside B is a natural compound with new pharmacological effects on improving endothelial dysfunction and treating vascular diseases.

摘要

据报道,酸枣仁皂苷B对多种心血管疾病具有保护作用。然而,酸枣仁皂苷B对血管张力和内皮功能的影响尚不清楚。本研究探讨了酸枣仁皂苷B降低血管张力、保护内皮功能的作用及其潜在机制。采用线式肌张力测定系统测量大鼠离体胸主动脉环的张力。采用Griess试剂法和酶联免疫吸附测定法测定人主动脉内皮细胞(HAECs)中一氧化氮(NO)浓度和内皮型一氧化氮合酶(eNOS)活性。采用蛋白质免疫印迹分析测定eNOS和丝氨酸1177位点磷酸化eNOS(p-eNOS)的蛋白水平。通过激光共聚焦成像显微镜测量HAECs中的细胞内Ca2+浓度。结果表明,酸枣仁皂苷B以剂量依赖性方式降低了完整内皮大鼠胸主动脉环的张力。L-硝基精氨酸甲酯(L-NAME)、KN93、乙二醇双四乙酸(EGTA)、SKF96365、iberiotoxin和格列本脲显著减弱了酸枣仁皂苷B诱导的完整内皮组织血管舒张。相反,吲哚美辛和4-二甲基氨基吡啶(4-DAMP)没有这种作用。酸枣仁皂苷B还促进NO生成并增加eNOS活性,L-NAME、EGTA和SKF96365可减弱这种作用。此外,酸枣仁皂苷B剂量依赖性地增加细胞内Ca2+浓度,EGTA和SKF96365可抑制这种增加。此外,在耗尽细胞内Ca2+储存后,酸枣仁皂苷B可立即诱导快速Ca2+内流,SKF96365可显著抑制这种内流。总之,本研究初步证实酸枣仁皂苷B以内皮依赖性方式降低血管张力。其潜在机制包括酸枣仁皂苷B通过内皮瞬时受体电位阳离子(TRPC)通道增加细胞外Ca2+内流,使eNOS磷酸化并促进血管内皮细胞中NO生成。此外,酸枣仁皂苷B诱导的血管舒张涉及通过内皮钾通道的内皮依赖性超极化。酸枣仁皂苷B是一种对改善内皮功能障碍和治疗血管疾病具有新药理作用的天然化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/632c/4762982/33d10e294ccc/pone.0149386.g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验