首页> 外文期刊>The American journal of Chinese medicine >Tetrahydroxystilbene Glucoside Inhibits Excessive Autophagy and Improves Microvascular Endothelial Dysfunction in Prehypertensive Spontaneously Hypertensive Rats
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Tetrahydroxystilbene Glucoside Inhibits Excessive Autophagy and Improves Microvascular Endothelial Dysfunction in Prehypertensive Spontaneously Hypertensive Rats

机译:四羟苯乙烯二糖苷抑制高血压前期自发性高血压大鼠过度自噬并改善微血管内皮功能障碍

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摘要

Autophagy exists in vascular endothelial cells, but the relationship between autophagy and blood vessel dysfunction in hypertension remains elusive. This study aimed to investigate role of autophagy in vascular endothelial dysfunction in prehypertension and hypertension and the underlying mechanisms involved. Furthermore, we sought to determine if and how tetrahydroxystilbene glucoside (TSG), a resveratrol analogue and active ingredient of Polygonum multiflorum Thunb used for its cardiovascular protective properties in traditional Chinese medicine, influences vascular endothelial function. Male spontaneously hypertensive rats (SHRs) aged 4 weeks (young) and 12 weeks (adult) were studied and the vascular function of isolated aorta and mesenteric artery was assessed in vitro. Compared with Wistar Kyoto rats (WKY), young and adult SHRs showed endothelial dysfunction of the aorta and mesenteric artery, along with decreased pAkt, pmTOR, and autophagic marker protein p62 and increased LC3 II/I in microvascular but not aortic tissues. TSG administration for 14 days significantly improved mesenteric vascular endothelial function, increased levels of pAkt and pmTOR, and decreased autophagy. Pretreatment of young SHRs with the mTOR inhibitor rapamycin blocked the antiautophagic and vasodilative effects of TSG. Moreover, TSG significantly activated Akt-mTOR signaling in HUVECs and reduced the autophagic levels in vitro, which were almost completely blocked by rapamycin. In summary, mesenteric endothelial dysfunction in prehypertensive SHRs was at least partly attributable to excessive autophagy in vascular tissues. TSG partly restored microvascular endothelial dysfunction through activating the Akt/mTOR pathway, which consequently suppressed autophagy, indicating that TSG could be potentially applied to protect vascular function against subclinical changes in prehypertension.
机译:自噬存在于血管内皮细胞中,但是自噬与高血压中血管功能障碍之间的关系仍然难以捉摸。这项研究旨在调查自噬在高血压前期和高血压中的血管内皮功能障碍中的作用及其涉及的潜在机制。此外,我们试图确定在传统中药中具有心血管保护作用的何首乌白藜芦醇类似物和有效成分四羟基二苯乙烯葡萄糖苷(TSG)是否以及如何影响血管内皮功能。研究了雄性自发性高血压大鼠(SHR),其年龄为4周(年轻)和12周(成人),并在体外评估了离体主动脉和肠系膜动脉的血管功能。与Wistar Kyoto大鼠(WKY)相比,年轻和成年SHRs表现出主动脉和肠系膜动脉的内皮功能障碍,同时pAkt,pmTOR和自噬标记蛋白p62降低,LC3 II / I在微血管中升高,但在主动脉组织中升高。 TSG给药14天可显着改善肠系膜血管内皮功能,增加pAkt和pmTOR的水平,并减少自噬。用mTOR抑制剂雷帕霉素预处理年轻的SHR,可以​​阻断TSG的抗自噬和血管舒张作用。此外,TSG可显着激活HUVEC中的Akt-mTOR信号传导,并降低体外自噬水平,而雷帕霉素几乎完全阻断了该水平。总之,高血压前SHRs的肠系膜内皮功能异常至少部分归因于血管组织过度自噬。 TSG通过激活Akt / mTOR通路部分恢复了微血管内皮功能障碍,从而抑制了自噬,这表明TSG可能被潜在地用于保护血管功能免受高血压前亚临床变化的影响。

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