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Physical Exercise Reduces the Expression of RANTES and Its CCR5 Receptor in the Adipose Tissue of Obese Humans

Authors :
Engin Baturcam
Naser Elkum
Kazem Behbehani
Jehad Abubaker
Samia Warsame
Cynthia Lehe
Jeena John
Irina Al-Khairi
Ali Tiss
Said Dermime
Maha M. Hammad
Mohamed Abu-Farha
Mohammed Dehbi
Abdelkrim Khadir
Preethi Cherian
Sina Kavalakatt
Fahad Al-Ghimlas
Source :
Mediators of Inflammation, Vol 2014 (2014), BASE-Bielefeld Academic Search Engine, Mediators of Inflammation
Publication Year :
2014
Publisher :
Hindawi Limited, 2014.

Abstract

RANTES and its CCR5 receptor trigger inflammation and its progression to insulin resistance in obese. In the present study, we investigated for the first time the effect of physical exercise on the expression of RANTES and CCR5 in obese humans. Fifty-seven adult nondiabetic subjects (17 lean and 40 obese) were enrolled in a 3-month supervised physical exercise. RANTES and CCR5 expressions were measured in PBMCs and subcutaneous adipose tissue before and after exercise. Circulating plasma levels of RANTES were also investigated. There was a significant increase in RANTES and CCR5 expression in the subcutaneous adipose tissue of obese compared to lean. In PBMCs, however, while the levels of RANTES mRNA and protein were comparable between both groups, CCR5 mRNA was downregulated in obese subjects (P<0.05). Physical exercise significantly reduced the expression of both RANTES and CCR5 (P<0.05) in the adipose tissue of obese individuals with a concomitant decrease in the levels of the inflammatory markers TNF-α, IL-6, and P-JNK. Circulating RANTES correlated negatively with anti-inflammatory IL-1ra (P=0.001) and positively with proinflammatory IP-10 and TBARS levels (P<0.05). Therefore, physical exercise may provide an effective approach for combating the deleterious effects associated with obesity through RANTES signaling in the adipose tissue.

Details

Language :
English
ISSN :
14661861 and 09629351
Volume :
2014
Database :
OpenAIRE
Journal :
Mediators of Inflammation
Accession number :
edsair.doi.dedup.....ab7000f51f8b1fa3b423e37eba349125