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Low macrophage accumulation in skeletal muscle of obese type 2 diabetics and elderly subjects.

Authors :
Tam CS
Sparks LM
Johannsen DL
Covington JD
Church TS
Ravussin E
Source :
Obesity (Silver Spring, Md.) [Obesity (Silver Spring)] 2012 Jul; Vol. 20 (7), pp. 1530-3. Date of Electronic Publication: 2012 Feb 08.
Publication Year :
2012

Abstract

In addition to adipose tissue, recent studies suggest that skeletal muscle may also be a source of low-grade inflammation, particularly in inactive and/or overweight individuals. The aim of this study was to examine the presence of macrophages in skeletal muscle from obese subjects with type 2 diabetes (T2D) before and after a 9-month exercise program (vs. a non-exercising control group) (Study 1) and in young vs. elderly subjects (Study 2). In both studies, CD68(+) macrophages in vastus lateralis biopsies were determined by immunohistochemistry and inflammation gene expression measured. Macrophage content (%) was calculated by the number of macrophages per 100 muscle fibers. In Study 1, we found relatively low numbers (2-3%) of CD68(+) macrophages in skeletal muscle in obese T2D subjects (BMI = 37.3 ± 5.2 kg/m(2)), which were unchanged after a 9-month exercise program (P = 0.42). Similarly, in Study 2 (BMI = 27.1 ± 2.5 kg/m(2)), CD68(+) macrophages were relatively low in muscle (4-5%) and were not different between young and elderly individuals (P = 0.42). However, elderly subjects had twofold higher CD68 and CD206 gene expression (both P < 0.002) than young participants. In both studies, CD68(+) muscle macrophages were not associated with BMI. In conclusion, we found little evidence of macrophage accumulation in skeletal muscle in obese T2D subjects or in elderly individuals. A 9-month exercise program was not associated with a decrease in macrophage content.

Details

Language :
English
ISSN :
1930-739X
Volume :
20
Issue :
7
Database :
MEDLINE
Journal :
Obesity (Silver Spring, Md.)
Publication Type :
Academic Journal
Accession number :
22314623
Full Text :
https://doi.org/10.1038/oby.2012.24