Chronic treatment with a carbon monoxide releasing molecule reverses dietary induced obesity in mice

被引:25
作者
Hosick, Peter A. [1 ,2 ]
AlAmodi, Abdulhadi A. [1 ,2 ]
Hankins, Michael W. [1 ,2 ]
Stec, David E. [1 ]
机构
[1] Univ Mississippi, Med Ctr, Ctr Excellence Cardiovasc Renal Res, Dept Physiol & Biophys, Jackson, MS 39216 USA
[2] Montclair State Univ, Dept Exercise Sci & Phys Educ, Montclair, NJ USA
关键词
metabolism; insulin resistance; inflammation; diabetes; carbon monoxide; IMPROVES INSULIN SENSITIVITY; CHRONIC ALLOGRAFT NEPHROPATHY; INCREASES ADIPONECTIN LEVELS; FATTY LIVER-DISEASE; MITOCHONDRIAL BIOGENESIS; HEME OXYGENASE; ADIPOSE-TISSUE; INDUCTION; PROTECTS; CO;
D O I
10.1080/21623945.2015.1038443
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Chronic, low level treatment with a carbon monoxide releasing molecule (CO-RM), CORM-A1, has been shown to prevent the development of obesity in response to a high fat diet. The objective of this study was to test the hypothesis that chronic, low level treatment with this CO-RM can reverse established obesity via a mechanism independent of food intake. Dietary induced obese mice were treated with CORM-A1, the inactive compound iCORM-A1, or saline every 48hours for 30 weeks while maintained on a high fat (60%) diet. Chronic treatment with CORM-A1 resulted in a 33% decrease from initial body weight over the 30 week treatment period while treatment with iCORM and saline were associated with 18 and 25% gain in initial body weight over the same time frame. Chronic treatment with CORM-A1 did not affect food intake or activity but resulted in a significant increase in metabolism. CORM-A1 treatment also resulted in lower fasting blood glucose, improvement in insulin sensitivity and decreased heptatic steatosis. Chronic treatment with CO releasing molecules can reverse dietary induced obesity and normalize insulin resistance independent of changes in food intake or activity. These findings are likely though a mechanism which increases metabolism.
引用
收藏
页码:1 / 10
页数:10
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