Interleukin-6-deficient mice develop mature-onset obesity

被引:972
作者
Wallenius, V
Wallenius, K
Ahrén, B
Rudling, M
Carlsten, H
Dickson, SL
Ohlsson, C
Jansson, JO [1 ]
机构
[1] Univ Gothenburg, Res Ctr Endocrinol & Metab, Sahlgrenska Acad, Gothenburg, Sweden
[2] Univ Gothenburg, Dept Rheumatol & Clin Immunol, Sahlgrenska Acad, Gothenburg, Sweden
[3] Lund Univ, Malmo Univ Hosp, Dept Med, Lund, Sweden
[4] Huddinge Univ Hosp, Karolinska Inst, Dept Gastroenterol, Stockholm, Sweden
[5] Univ Cambridge, Dept Physiol, Cambridge, England
基金
英国医学研究理事会;
关键词
D O I
10.1038/nm0102-75
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The immune-modulating cytokine interleukin-6 (IL-6) its expressed both in adipose tissue and centrally in hypothalamic nuclei that regulate body composition. We investigated the impact of loss of IL-6 on body composition in mice lacking the gene encoding IL-6 (116(-/-) mice) and found that they developed mature-onset obesity that was partly reversed by IL-6 replacement: The obese 116(-/-) mice had disturbed carbohydrate and lipid metabolism, increased leptin levels and decreased responsiveness to leptin treatment. To investigate the possible mechanism and site of action of the anti-obesity effect of IL-6, we injected rats centrally and peripherally with IL-6 at low doses. Intracerebroventricular, but not intraperitoneal IL-6 treatment increased energy expenditure. In conclusion, centrally acting IL-6 exerts anti-obesity effects in rodents.
引用
收藏
页码:75 / 79
页数:5
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