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四氢呋喃葡萄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。

Tetrahydroxystilbene Glucoside Inhibits Excessive Autophagy and Improves Microvascular Endothelial Dysfunction in Prehypertensive Spontaneously Hypertensive Rats.

机构信息

* Department of Natural Medicine, School of Pharmacy, Fourth Military Medical University, Xi'an 710032, P.R. China.

† Department of Physiology, Fourth Military Medical University, Xi'an 710032, P.R. China.

出版信息

Am J Chin Med. 2016;44(7):1393-1412. doi: 10.1142/S0192415X16500786. Epub 2016 Oct 25.

Abstract

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.

摘要

自噬存在于血管内皮细胞中,但自噬与高血压血管功能障碍之间的关系仍不清楚。本研究旨在探讨自噬在高血压前期和高血压血管内皮功能障碍中的作用及其潜在机制。此外,我们还试图确定,白藜芦醇类似物和何首乌的有效成分二苯乙烯苷(TSG),是否以及如何影响血管内皮功能。二苯乙烯苷在传统中药中因其心血管保护特性而被使用。我们研究了 4 周龄(幼年期)和 12 周龄(成年期)的自发性高血压大鼠(SHR),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 京都大鼠(WKY)相比,幼年期和成年期 SHR 的主动脉和肠系膜动脉内皮功能障碍,微血管而非主动脉组织中 pAkt、pmTOR 和自噬标记蛋白 p62 减少,LC3 II/I 增加。14 天的 TSG 给药显著改善了肠系膜血管内皮功能,增加了 pAkt 和 pmTOR 的水平,并减少了自噬。用 mTOR 抑制剂雷帕霉素预处理幼年期 SHR 阻断了 TSG 的抗自噬和血管舒张作用。此外,TSG 显著激活了 HUVECs 中的 Akt-mTOR 信号通路,并减少了体外的自噬水平,而这一作用几乎被雷帕霉素完全阻断。综上所述,高血压前期 SHR 的肠系膜内皮功能障碍至少部分归因于血管组织中过度的自噬。TSG 通过激活 Akt/mTOR 通路部分恢复微血管内皮功能障碍,从而抑制自噬,表明 TSG 可能潜在地应用于保护血管功能,防止高血压前期的亚临床变化。

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