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二肽基肽酶IV抑制剂作为血管疾病的新型调节剂

Dipeptidyl peptidase IV inhibitors as novel regulators of vascular disease.

作者信息

Akoumianakis Ioannis, Antoniades Charalambos

机构信息

Division of Cardiovascular Medicine, University of Oxford, UK.

Division of Cardiovascular Medicine, University of Oxford, UK.

出版信息

Vascul Pharmacol. 2017 Sep;96-98:1-4. doi: 10.1016/j.vph.2017.07.001. Epub 2017 Jul 8.

Abstract

Dipeptidyl peptidase IV (DPP-IV) has been revealed as an adipokine with potential relevance in cardiovascular disease (CVD), while clinically used DPP-IV inhibitors have demonstrated beneficial cardiovascular effects in several experimental studies. Perivascular adipose tissue (PVAT) is a unique adipose tissue depot in close anatomical proximity and bidirectional functional interaction with the vascular wall, which is a source of DPP-IV and its biology may be influenced by DPP-IV inhibition. Recently, DPP-IV inhibition has been associated with decreased local inflammation and oxidative stress both in the vascular wall and the PVAT, potentially regulating atherogenesis progression in vivo. DPP-IV inhibition may thus be a promising target in cardiovascular disease. However, the exact pleiotropic mechanisms that underlie the cardiovascular effects of DPP-IV inhibition need to be clarified, while the in vivo benefit of DPP-IV inhibition in humans remains unclear.

摘要

二肽基肽酶IV(DPP-IV)已被证实是一种与心血管疾病(CVD)潜在相关的脂肪因子,而临床使用的DPP-IV抑制剂在多项实验研究中已显示出有益的心血管效应。血管周围脂肪组织(PVAT)是一种独特的脂肪组织库,在解剖学上与血管壁紧密相邻且存在双向功能相互作用,它是DPP-IV的来源,其生物学特性可能会受到DPP-IV抑制的影响。最近,DPP-IV抑制与血管壁和PVAT中局部炎症及氧化应激的降低相关,这可能在体内调节动脉粥样硬化的进展。因此,DPP-IV抑制可能是心血管疾病中一个有前景的靶点。然而,DPP-IV抑制产生心血管效应的确切多效性机制尚需阐明,同时DPP-IV抑制对人类的体内益处仍不明确。

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