Key result
Perivascular adipose tissue regulates vascular tone by releasing vasoactive mediators, with its secretory profile altered in obesity and cardiovascular diseases to favor pro-contractile effects.
Perivascular adipose tissue plays an active role in vascular homeostasis, with its secretory profile shifting towards pro-contractile effects in obesity and cardiovascular diseases.
May contribute to vascular complications in obesity; leaves open whether PVAT-targeted therapies improve outcomes.
Perivascular adipose tissue (PVAT) is now recognized as an active player in vascular homeostasis. The expansion of PVAT in obesity and its possible role in vascular dysfunction have attracted much interest. In terms of the regulation of vascular tone and blood pressure, PVAT has been shown to release vasoactive mediators, for instance, angiotensin peptides, reactive oxygen species, chemokines and cytokines. The secretory profile of PVAT is altered by obesity, hypertension and other cardiovascular diseases, leading to an imbalance between its pro-contractile and anti-contractile effects. PVAT adipocytes represent an important source of the mediators, but infiltrating immune cells may become more important under conditions of hypoxia and inflammation. This review describes recent advances in the effects of PVAT on the regulation of vascular tone, highlighting the evidence for a pro-contractile action in health and disease. The role of the endothelium, vascular smooth muscle, immune cells and probably perivascular nerves in PVAT function is also discussed. LINKED ARTICLES: This article is part of a themed section on Molecular Mechanisms Regulating Perivascular Adipose Tissue - Potential Pharmacological Targets? To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v174.20/issuetoc.
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Ramirez et al. (2017) conducted a review in Obesity, hypertension, and cardiovascular diseases. Perivascular adipose tissue (PVAT) was evaluated. Perivascular adipose tissue regulates vascular tone by releasing vasoactive mediators, with its secretory profile altered in obesity and cardiovascular diseases to favor pro-contractile effects.
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