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Perivascular Adipose Tissue as an Indication, Contributor to, and Therapeutic Target for Atherosclerosis.

作者信息

Liu Yan, Sun Yan, Hu Chengping, Liu Jinxing, Gao Ang, Han Hongya, Chai Meng, Zhang Jianwei, Zhou Yujie, Zhao Yingxin

机构信息

Department of Cardiology, Beijing Anzhen Hospital, Capital Medical University, Beijing Institute of Heart Lung and Blood Vessel Disease, Beijing, China.

出版信息

Front Physiol. 2020 Dec 18;11:615503. doi: 10.3389/fphys.2020.615503. eCollection 2020.


DOI:10.3389/fphys.2020.615503
PMID:33391033
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7775482/
Abstract

Perivascular adipose tissue (PVAT) has been identified to have significant endocrine and paracrine functions, such as releasing bioactive adipokines, cytokines, and chemokines, rather than a non-physiological structural tissue. Considering the contiguity with the vascular wall, PVAT could play a crucial role in the pathogenic microenvironment of atherosclerosis. Growing clinical evidence has shown an association between PVAT and atherosclerosis. Moreover, based on computed tomography, the fat attenuation index of PVAT was verified as an indication of vulnerable atherosclerotic plaques. Under pathological conditions, such as obesity and diabetes, PVAT shows a proatherogenic phenotype by increasing the release of factors that induce endothelial dysfunction and inflammatory cell infiltration, thus contributing to atherosclerosis. Growing animal and human studies have investigated the mechanism of the above process, which has yet to be fully elucidated. Furthermore, traditional treatments for atherosclerosis have been proven to act on PVAT, and we found several studies focused on novel drugs that target PVAT for the prevention of atherosclerosis. Emerging as an indication, contributor to, and therapeutic target for atherosclerosis, PVAT warrants further investigation.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5f1/7775482/1683efb01f94/fphys-11-615503-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5f1/7775482/1683efb01f94/fphys-11-615503-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5f1/7775482/1683efb01f94/fphys-11-615503-g001.jpg

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[1]
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[2]
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本文引用的文献

[1]
Anti-inflammatory and anti-proliferative action of adiponectin mediated by insulin signaling cascade in human vascular smooth muscle cells.

Mol Biol Rep. 2020-9

[2]
Modulation of Vascular Function by Perivascular Adipose Tissue: Sex Differences.

Curr Pharm Des. 2020

[3]
The Role of High-Density Lipoproteins in Endothelial Cell Metabolism and Diabetes-Impaired Angiogenesis.

Int J Mol Sci. 2020-5-21

[4]
Empagliflozin ameliorates endothelial dysfunction and suppresses atherogenesis in diabetic apolipoprotein E-deficient mice.

Eur J Pharmacol. 2020-5-15

[5]
Dietary Ethanolic Extract of Reduces VCAM-1, Perivascular Adipose Tissue and Aortic Intimal Medial Thickness in Hypercholesterolemic Rat Model.

Open Access Maced J Med Sci. 2019-10-10

[6]
Age-Dependent and -Independent Effects of Perivascular Adipose Tissue and Its Paracrine Activities during Neointima Formation.

Int J Mol Sci. 2019-12-31

[7]
Estrogenic and anti-inflammatory effects of pseudoprotodioscin in atherosclerosis-prone mice: Insights into endothelial cells and perivascular adipose tissues.

Eur J Pharmacol. 2019-12-23

[8]
B Lymphocytes and Macrophages in the Perivascular Adipose Tissue Are Associated With Coronary Atherosclerosis: An Autopsy Study.

J Am Heart Assoc. 2019-12-10

[9]
The Influence of Photoperiod on the Action of Exogenous Leptin on Gene Expression of Proinflammatory Cytokines and Their Receptors in the Thoracic Perivascular Adipose Tissue (PVAT) in Ewes.

Mediators Inflamm. 2019-11-12

[10]
Revisiting carotid imaging: integrating atherosclerosis, the adventitia, and perivascular adipose tissue.

Kardiol Pol. 2019-11-22

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