The english version of the website is under development. Wherever text appears in Greek, it means it has not been translated yet.

Δημοσίευση

Should adipokines be considered in the choice of the treatment of obesity-related health problems?

TitleShould adipokines be considered in the choice of the treatment of obesity-related health problems?
Publication TypeJournal Article
Year of Publication2010
AuthorsAthyros, V. G., Tziomalos K., Karagiannis A., Anagnostis P., & Mikhailidis D. P.
JournalCurr Drug Targets
Volume11
Issue1
Pagination122-35
Date Published2010 Jan
ISSN1873-5592
KeywordsAdipokines, Animals, Biological Markers, Cardiovascular Diseases, Diabetes Mellitus, Type 2, Humans, Obesity
Abstract

White adipose tissue (WAT) is an important endocrine organ that secretes approximately 30 biologically active peptides and proteins, collectively termed "adipokines". These are either produced exclusively by WAT (mainly adiponectin, leptin and resistin) or also by other tissues [e.g. tumour necrosis factor (TNF)-alpha, interleukin (IL)-6, plasminogen activator inhibitor (PAI)-1, angiotensinogen]. Adipokines play a central role in body homeostasis including the regulation of food intake and energy balance, insulin action, lipid and glucose metabolism, angiogenesis and vascular remodelling, regulation of blood pressure and coagulation. Excess WAT, especially visceral obesity, is linked to obesity-related health problems through insulin resistance (IR) [leading to type 2 diabetes mellitus (T2DM)] and systemic low-grade inflammation [leading to cardiovascular disease (CVD)]. The adipokines are important mediators of these adverse effects. This review describes the role of proinflammatory adipokines in the pathogenesis of IR and of the chronic inflammatory state associated with visceral obesity. Moreover, it summarises treatment options for the normalisation of adipokine levels, which might confer an additional clinical benefit in the effort to prevent or treat obesity-related T2DM and CVD.

Alternate JournalCurr Drug Targets
PubMed ID20017725

Contact

Secretariat of the School of Medicine
 

Connect

School of Medicine's presence in social networks
Follow Us or Connect with us.