Abstract
The melanocortin system is a critical pathway in the regulation of energy balance. In this study, we analyzed the peripheral effects of the synthetic melanocortin agonist melanotan-II (MT-II) in rodents fed a low-fat or high-fat diet. MT-II-treated high-fat diet-induced obese (DIO) mice lost weight and body fat, whereas MT-II-treated low-fat-fed mice maintained their original body weight. Specifically, MT-II treatment led to a general reduction in both visceral and subcutaneous adipose tissue in high-fat-fed mice compared with Vehicle (ad libitum) controls. Vehicle-treated pair-fed DIO mice lost an equivalent amount of body weight compared with MT-II-treated mice but retained more adipose tissue. Pair-fed mice showed a reduction in visceral adipose tissue and no effect on subcutaneous adipose tissue compared with MT-II-treated mice. It is surprising that subcutaneous lean mass was significantly reduced in the pairfed mice. The data were replicated in DIO rats and indicated that MT-II treatment led to a generalized reduction in adipose tissue. These results indicate that peripheral MT-II treatment leads to weight loss that affects both the visceral and subcutaneous fat compartments. This finding illustrates the complexity of analyzing weight-reducing compounds. Although the present data suggest that the anorectic effect of MT-II is primarily a consequence of reduced food intake, the body composition data suggest that other mechanisms are involved.
Footnotes
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This work was supported by NIDDK, National Institutes of Health Grants DK54890 and DK56863 (to R.J.S.).
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Article, publication date, and citation information can be found at http://jpet.aspetjournals.org.
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doi:10.1124/jpet.107.123091.
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ABBREVIATIONS: MC3R, melanocortin-3; MC4R, melanocortin-4 receptor; MT-II, melanotan-II; DIO, diet-induced obese; PBS, phosphate-buffered saline; HF, high-fat; LF, low-fat; α-MSH, α-melanocyte-stimulating hormone; AgRP, agouti-related peptide; EWAT, epididymal white adipose tissue; IWAT, inguinal white adipose tissue; ANOVA, analysis of variance; bp, base pair; SHU9119, [Ac-Nle-c[Asp-His-d-Nal(2′)-Arg-Trp-Lys]-NH2].
- Received March 20, 2007.
- Accepted June 12, 2007.
- The American Society for Pharmacology and Experimental Therapeutics
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