Akoumianakis Ioannis, Antoniades Charalambos
Division of Cardiovascular Medicine, University of Oxford, UK.
Division of Cardiovascular Medicine, University of Oxford, UK.
Vascul Pharmacol. 2017 Sep;96-98:1-4. doi: 10.1016/j.vph.2017.07.001. Epub 2017 Jul 8.
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.
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。