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Similarity of mouse perivascular and brown adipose tissues and their resistance to diet-induced inflammation

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TLDR
In this article, perivascular adipose tissue (PVAT) is a unique adipose depot that likely influences vascular function and susceptibility to pathogenesis in obesity and metabolic syndrome.
Abstract
Thoracic perivascular adipose tissue (PVAT) is a unique adipose depot that likely influences vascular function and susceptibility to pathogenesis in obesity and the metabolic syndrome. Surprisingly...

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Adipose Tissue Distribution, Inflammation and Its Metabolic Consequences, Including Diabetes and Cardiovascular Disease.

TL;DR: The mechanisms by which dysfunctional adipose tissue simultaneously promote T2DM and CVD, focusing on adipose tissues depot-specific adipokines, inflammatory profiles, and metabolism, will be the focus of this review.
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Control of brown and beige fat development

TL;DR: F Fate-mapping analyses have identified progenitor populations that give rise to brown and beige fat cells, and have revealed unanticipated cell-lineage relationships between vascular smooth muscle cells and bege adipocytes, and between skeletal Muscle cells and brown fat.
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Obesity-Induced Changes in Adipose Tissue Microenvironment and Their Impact on Cardiovascular Disease

TL;DR: This review focuses on the microenvironment of adipose tissue and how it influences cardiovascular disorders, including atherosclerosis and ischemic heart diseases, through the systemic actions of adipokines.
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What causes the insulin resistance underlying obesity

TL;DR: The need to better understand the mechanisms linking visceral adiposity with liver fat accumulation, the mechanisms by which ectopic fat accumulation cause insulin resistance, and the size of adipose tissue depots is determined is underscored.
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The Vascular Endothelium of the Adipose Tissue Gives Rise to Both White and Brown Fat Cells

TL;DR: It is found that murine endothelial cells of classic white and brown fat depots share ultrastructural characteristics with pericytes, which are pluripotent and can potentially give rise to preadipocytes, suggesting an endothelial origin of murine and human adipocytes.
References
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Journal ArticleDOI

Vascular-associated lymphoid tissue (VALT) involvement in aortic aneurysm.

TL;DR: The present observations show that in aortic aneurysm, VALT is involved in immune responses and its activation mostly occurs in the adventitia, which suggests that VALT might locally serve the entire complex of both cellular and humoral immune responses in theAneurysmal wall.
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Biochemical basis of fat cell insulin resistance in obese rodents and man

TL;DR: It is striking that fat cells from young, 4–7-wk-old obob mice actually exhibit increased responsiveness to the action of insulin on glucose transport and metabolism when their capacity for fatty acid synthesis is exceedingly high, and it seems possible that this amplified responsiveness to insulin in these very young Obob mice may be intimately involved in the etiology of this obese syndrome.
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Circulating retinol-binding protein 4 and subclinical cardiovascular disease in the elderly.

TL;DR: Circulating RBP4 concentrations were inversely associated with intima-media and plaque echogenicity in carotid arteries, implying that RBP 4 could be involved in the development of atherosclerosis.
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Impact of obesity on revascularization and restenosis rates after bare-metal and drug-eluting stent implantation (from the TAXUS-IV trial).

TL;DR: Obesity is an important risk factor for clinical and angiographic restenosis and for composite major adverse cardiac events in patients who receive bare-metal stents andPaclitaxel-eluting stents attenuate the increased risk associated with obesity, such that the intermediate-term prognosis after percutaneous coronary intervention is independent of weight.
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Estrogen Attenuates Integrin-β3–Dependent Adventitial Fibroblast Migration After Inhibition of Osteopontin Production in Vascular Smooth Muscle Cells

TL;DR: It is suggested that estrogen indirectly attenuates integrin-beta(3)-dependent adventitial fibroblast migration after inhibition of OPN expression in activated VSMCs.
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