Subcutaneous and visceral adipose tissue: structural and functional differences
- PMID: 19656312
- DOI: 10.1111/j.1467-789X.2009.00623.x
Subcutaneous and visceral adipose tissue: structural and functional differences
Abstract
Obesity is a heterogeneous disorder. Obese individuals vary in their body fat distribution, their metabolic profile and degree of associated cardiovascular and metabolic risk. Abdominal obesity carries greater risk of developing diabetes and future cardiovascular events than peripheral or gluteofemoral obesity. There are differences between adipose tissue present in subcutaneous areas (SCAT) and visceral adipose tissue (VAT) present in the abdominal cavity. These include anatomical, cellular, molecular, physiological, clinical and prognostic differences. Anatomically, VAT is present mainly in the mesentery and omentum, and drains directly through the portal circulaion to the liver. VAT compared with SCAT is more cellular, vascular, innervated and contains a larger number of inflammatory and immune cells, lesser preadipocyte differentiating capacity and a greater percentage of large adipocytes. There are more glucocorticoid and androgen receptors in VAT than in SCAT. VAT adipocytes are more metabolically active, more sensitive to lipolysis and more insulin-resistant than SCAT adipocytes. VAT has a greater capacity to generate free fatty acids and to uptake glucose than SCAT and is more sensitive to adrenergic stimulation, while SCAT is more avid in absorption of circulating free fatty acids and triglycerides. VAT carries a greater prediction of mortality than SCAT.
Similar articles
-
Depot-specific hormonal characteristics of subcutaneous and visceral adipose tissue and their relation to the metabolic syndrome.Horm Metab Res. 2002 Nov-Dec;34(11-12):616-21. doi: 10.1055/s-2002-38256. Horm Metab Res. 2002. PMID: 12660870 Review.
-
Contributions of total body fat, abdominal subcutaneous adipose tissue compartments, and visceral adipose tissue to the metabolic complications of obesity.Metabolism. 2001 Apr;50(4):425-35. doi: 10.1053/meta.2001.21693. Metabolism. 2001. PMID: 11288037 Clinical Trial.
-
The fatty acid transporter FAT/CD36 is upregulated in subcutaneous and visceral adipose tissues in human obesity and type 2 diabetes.Int J Obes (Lond). 2006 Jun;30(6):877-83. doi: 10.1038/sj.ijo.0803212. Int J Obes (Lond). 2006. PMID: 16418758
-
Deep subcutaneous adipose tissue: a distinct abdominal adipose depot.Obesity (Silver Spring). 2007 Aug;15(8):1933-43. doi: 10.1038/oby.2007.231. Obesity (Silver Spring). 2007. PMID: 17712110
-
Impact of visceral adipose tissue on liver metabolism. Part I: heterogeneity of adipose tissue and functional properties of visceral adipose tissue.Diabetes Metab. 2008 Sep;34(4 Pt 1):317-27. doi: 10.1016/j.diabet.2008.04.001. Epub 2008 Jun 11. Diabetes Metab. 2008. PMID: 18550411 Review.
Cited by
-
High Subcutaneous Adipose Tissue Radiodensity Predicts Poor Prognosis in Patients With Gastric Cancer.Cancer Diagn Progn. 2024 Nov 3;4(6):754-761. doi: 10.21873/cdp.10392. eCollection 2024 Nov-Dec. Cancer Diagn Progn. 2024. PMID: 39502618 Free PMC article.
-
Functional Dentition and 12-Month Changes in Body Measurements among Thai Older Adults.Int J Environ Res Public Health. 2020 Jun 12;17(12):4200. doi: 10.3390/ijerph17124200. Int J Environ Res Public Health. 2020. PMID: 32545560 Free PMC article.
-
Lipofilling in Breast Oncological Surgery: A Safe Opportunity or Risk for Cancer Recurrence?Int J Mol Sci. 2021 Apr 3;22(7):3737. doi: 10.3390/ijms22073737. Int J Mol Sci. 2021. PMID: 33916703 Free PMC article. Review.
-
Co-methylated genes in different adipose depots of pig are associated with metabolic, inflammatory and immune processes.Int J Biol Sci. 2012;8(6):831-7. doi: 10.7150/ijbs.4493. Epub 2012 Jun 10. Int J Biol Sci. 2012. PMID: 22719223 Free PMC article.
-
Association between type 2 diabetes mellitus and body composition based on MRI fat fraction mapping.Front Public Health. 2024 Jan 23;12:1332346. doi: 10.3389/fpubh.2024.1332346. eCollection 2024. Front Public Health. 2024. PMID: 38322122 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical