Paracrine regulation of vascular tone, inflammation and insulin sensitivity by perivascular adipose tissue

被引:76
|
作者
Eringa, Etto C. [1 ]
Bakker, Wineke [1 ]
van Hinsbergh, Victor W. M. [1 ]
机构
[1] Vrije Univ Amsterdam Med Ctr, Inst Cardiovasc Res, Physiol Lab, Amsterdam, Netherlands
关键词
Adipose tissue; Endothelium; Insulin; Vasoregulation; Adipokines; PROTEIN-KINASE-C; NITRIC-OXIDE SYNTHASE; ENDOTHELIAL-CELLS; METABOLIC SYNDROME; FAT; RESISTANCE; EXPRESSION; ACTIVATION; ADIPONECTIN; DYSFUNCTION;
D O I
10.1016/j.vph.2012.02.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A small amount of adipose tissue associated with small arteries and arterioles is encountered both in mice and man. This perivascular adipose tissue (PVAT) has a paracrine effect on the vascular tone regulation. PVAT is expanded in obesity and in diabetes. This expansion not only involves enlargement of fat cells, but also the accumulation of inflammatory cells and a shift in the production of adipokines and cytokines. This effect is illustrated in this review by the effect of PVAT-derived factors of insulin-mediated vasoregulation in mouse resistance arteries. Insulin sensitivity of endothelial cells is also involved in the insulin-mediated regulation of muscle glucose uptake. Insulin affects vasoregulation by acting on different signaling pathways regulating NO and endothelin-1 release. This process is influenced by various adipokines and inflammatory mediators released from PVAT, and is affected by the degree of expansion and content of inflammatory cells. It is modulated by adiponectin (via 5' adenosine monophosphate-activated protein kinase, AMPK), TNF alpha (via c-jun N-terminal kinase) and free fatty acids (via protein kinase C-theta). PVAT thus provides an important site of control of vascular (dys)function in obesity and type 2 diabetes. An altered profile of adipokine and cytokine production by PVAT of resistance arteries may also contribute to or modulate hypertension, but a causal role in hypertension has still to be established. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:204 / 209
页数:6
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