首页> 美国卫生研究院文献>other >Blood Pressure-Lowering Peptides from Neo-Fermented Buckwheat Sprouts: A New Approach to Estimating ACE-Inhibitory Activity
【2h】

Blood Pressure-Lowering Peptides from Neo-Fermented Buckwheat Sprouts: A New Approach to Estimating ACE-Inhibitory Activity

机译:新发酵的荞麦芽中降血压肽:一种估计ACE抑制活性的新方法

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Neo-fermented buckwheat sprouts (neo-FBS) contain angiotensin-converting enzyme (ACE) inhibitors and vasodilators with blood pressure-lowering (BPL) properties in spontaneously hypertensive rats (SHRs). In this study, we investigated antihypertensive mechanisms of six BPL peptides isolated from neo-FBS (FBPs) by a vasorelaxation assay and conventional in vitro, in vivo, and a new ex vivo ACE inhibitory assays. Some FBPs demonstrated moderate endothelium-dependent vasorelaxation in SHR thoracic aorta and all FBPs mildly inhibited ACE in vitro. Orally administered FBPs strongly inhibited ACE in SHR tissues. To investigate detailed ACE-inhibitory mechanism of FBPs in living body tissues, we performed the ex vivo assay by using endothelium-denuded thoracic aorta rings isolated from SHRs, which demonstrated that FBPs at low concentration effectively inhibited ACE in thoracic aorta tissue and suppressed angiotensin II-mediated vasoconstriction directly associated with BPL. These results indicate that the main BPL mechanism of FBP was ACE inhibition in living body tissues, suggesting that high FBP's bioavailability including absorption, tissue affinity, and tissue accumulation was responsible for the superior ACE inhibition in vivo. We propose that our ex vivo assay is an efficient and reliable method for evaluating ACE-inhibitory mechanism responsible for BPL activity in vivo.
机译:新发酵的荞麦芽(neo-FBS)含有自发性高血压(SHRs)具有降血压(BPL)特性的血管紧张素转换酶(ACE)抑制剂和血管扩张剂。在这项研究中,我们调查了通过血管舒张测定法和常规的体外,体内及新的离体ACE抑制测定法从neo-FBS(FBP)分离的六个BPL肽的降压机制。一些FBP在SHR胸主动脉中表现出中度内皮依赖性血管舒张作用,并且所有FBP在体外均轻度抑制ACE。口服FBP强烈抑制SHR组织中的ACE。为了研究FBPs在活体组织中的详细ACE抑制机制,我们通过使用从SHRs中分离的内皮剥脱的胸主动脉环进行了离体试验,这表明低浓度的FBPs有效抑制了胸主动脉组织中的ACE并抑制了血管紧张素II介导的血管收缩与BPL直接相关。这些结果表明,FBP的主要BPL机制是活体组织中的ACE抑制,这表明高FBP的生物利用度(包括吸收,组织亲和力和组织积累)是体内ACE抑制作用的原因。我们建议我们的离体测定是一种有效而可靠的方法,用于评估负责体内BPL活性的ACE抑制机制。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号