Suppr超能文献

葡萄籽原花青素提取物通过 5'-AMP 激活蛋白激酶/ SURT1-Krüpple 样因子 2 通路增强内皮型一氧化氮合酶表达,并调节哇巴因诱导的高血压大鼠的血压。

Grape seed proanthocyanidin extracts enhance endothelial nitric oxide synthase expression through 5'-AMP activated protein kinase/Surtuin 1-Krüpple like factor 2 pathway and modulate blood pressure in ouabain induced hypertensive rats.

机构信息

Department of Geriatrics, Qilu Hospital of Shandong University, Jinan, Shandong Province 250012, China.

出版信息

Biol Pharm Bull. 2012;35(12):2192-7. doi: 10.1248/bpb.b12-00598. Epub 2012 Sep 14.

Abstract

Grape seed proanthocyanidin extracts (GSPE) belonging to polyphenols, possess various biological effects including anti-inflammation, anti-oxidant, anti-aging, anti-atherosclerosis, etc. GSPE is potential in regulating endothelial function. However, the underlying mechanism is not clear yet. In this study, by small interfering RNA (siRNA) knocking down, we proved that GSPE increase endothelial nitric oxide synthase (eNOS) expression in human umbilical vessel cells (HUVECs) in vitro, which was attributed to its transcription factor Krüpple like factor 2 (KLF2) induction. Furthermore, GSPE activate 5'-AMP activated protein kinase (AMPK) and increase surtuin 1 (SIRT1) protein level, critical for KLF2 induction. We also illuminated the role of GSPE in hypertension treatment. By chronic administration of GSPE in ouabain induced hypertensive rats model, we access the effect of GSPE on blood pressure regulation and the possible mechanisms involved. After 5 weeks feeding, GSPE significantly block the ouabain induced blood pressure increase. The aortic NO production impaired by ouabain was improved. In conclusion, GSPE increase eNOS expression and NO production in an AMPK/SIRT1 dependent manner through KLF2 induction, and attenuate ouabain induced hypertension.

摘要

葡萄籽原花青素提取物(GSPE)属于多酚类物质,具有多种生物学效应,包括抗炎、抗氧化、抗衰老、抗动脉粥样硬化等。GSPE 可能在调节内皮功能方面发挥作用。然而,其潜在机制尚不清楚。在这项研究中,我们通过小干扰 RNA(siRNA)敲低,证明 GSPE 在体外可增加人脐静脉细胞(HUVEC)中的内皮型一氧化氮合酶(eNOS)表达,这归因于其转录因子 Krüpple 样因子 2(KLF2)的诱导。此外,GSPE 可激活 5'-AMP 激活蛋白激酶(AMPK)并增加 SIRT1 蛋白水平,这对于 KLF2 的诱导至关重要。我们还阐明了 GSPE 在高血压治疗中的作用。通过在哇巴因诱导的高血压大鼠模型中进行 GSPE 的慢性给药,我们评估了 GSPE 对血压调节的影响及其可能涉及的机制。经过 5 周的喂养,GSPE 显著阻断了哇巴因引起的血压升高。哇巴因引起的主动脉 NO 产生受损得到改善。总之,GSPE 通过诱导 KLF2 以 AMPK/SIRT1 依赖的方式增加 eNOS 表达和 NO 产生,并减轻哇巴因诱导的高血压。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验