Cited by 54Cardiovascular Disease and AdiposityAdipokines, Inflammation, and Metabolic DiseasesNitric Oxide and Endothelin Effects

Dysfunction of human subcutaneous fat arterioles in obesity alone or obesity associated with type 2 diabetes

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Georgescu, Adriana, Popov, Doina, Constantin, Anamaria, Nemecz, Miruna, Alexandru, Nicoleta, Cochior, Daniel, Tudor, Aura·2011·Clinical Science

Abstract

The aim of the present study was to examine the effects of obesity alone and obesity associated with Type 2 diabetes on the structure, vascular reactivity and response to insulin of isolated human subcutaneous fat arterioles; these effects were correlated with the expression of insulin signalling proteins. Periumbilical subcutaneous adipose tissue was explanted during surgery, small arterioles (internal diameter 220 ± 40 μm) were dissected out and investigated by electron microscopy, myography and immunoblotting. Compared with the subcutaneous arterioles of lean subjects, obesity activated the endothelium, enhanced the accumulation of collagen within vascular wall and increased the sensitivity of adrenergic response; obesity also diminished eNOS (endothelial NO synthase) protein expression, NO production, and endothelium-dependent and insulin-induced vasodilatation, as well as the protein expression of both IRS (insulin receptor substrates)-1 and IRS-2 and of the downstream molecules in the insulin signalling pathway, such as PI3K (phosphoinositide 3-kinase), phospho-Akt and Akt. When obesity was associated with Type 2 diabetes, these changes were significantly augmented. In conclusion, obesity alone or obesity associated with Type 2 diabetes alters human periumbilical adipose tissue arterioles in terms of structure, function and biochemsitry, including diminished eNOS expression and reduced levels of IRS-1, IRS-2, PI3K and Akt in the insulin signalling pathway.

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Crossref · 10.1042/cs20100355

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  • Lower NOS3 abundance is found in both adipose tissue and skeletal muscle of obese humans and rodents.

    “lower NOS3 abundance is found in both adipose tissue and skeletal muscle of obese humans and rodents [120-124].”

    From Regulation of obesity and insulin resistance by nitric oxide (2014) · cites this paper as [120]

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References 25 · Cited by 54

Authors
Georgescu, A., Popov, D., Constantin, A., Nemecz, M., Alexandru, N., Cochior, D., & Tudor, A.
Affiliations
  • Institutul de Chimie Macromoleculară Petru Poni (RO)
  • Romanian Academy (RO)
  • CFR 2 University Hospital, Bucharest, Romania
Corresponding author
  • Georgescu, Adriana
  • Alexandru, Nicoleta
Venue
Clinical Science
Published
2011-01-28
Volume
120
Issue
10
Pages
463-472
ISSN
  • 0143-5221 (ISSN-L)
  • 1470-8736
OpenAlex
W1976982043
Cited by
54
References
25
Citations by year
2026: 1 · 2024: 2 · 2022: 4 · 2021: 2 · 2020: 2 · 2019: 3 · 2018: 4 · 2017: 4 · 2016: 6 · 2015: 6 · 2014: 5 · 2013: 5 · 2012: 8
FWCI
3.29
Type
journal article
Language
en
Open access
Licence
other-oa
Locations
  • Clinical Science (publishedVersion)
  • PubMed (publishedVersion)
  • HAL (submittedVersion, other-oa)
  • Trinity's Access to Research Output (TARA) (Trinity College Dublin) (submittedVersion)
Funders
Universitatea din București
Topics
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiovascular Disease and Adiposity
  • Health Sciences › Medicine › Epidemiology › Adipokines, Inflammation, and Metabolic Diseases
  • Health Sciences › Medicine › Physiology › Nitric Oxide and Endothelin Effects
Keywords
obesity, type 2 diabetes, subcutaneous adipose tissue, vascular dysfunction, endothelial dysfunction, insulin signaling, IRS-1, insulin receptor substrate 2, PI3K/Akt signaling, endothelial nitric oxide synthase, nitric oxide, adrenergic vasoconstriction, collagen deposition
MeSH terms
Adult, Arterioles, Diabetes Mellitus, Type 2, Endothelium, Vascular, Female, Humans, Insulin, Male, Middle Aged, Myography, Nitric Oxide, Norepinephrine, Obesity, Vasoconstriction, Vasoconstrictor Agents, Signal Transduction, Case-Control Studies, Subcutaneous Fat, Nitric Oxide Synthase Type III

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