Role of leptin and melanocortin signaling in uremia-associated cachexia.

Cheung W, Yu PX, Little BM, Cone RD, Marks DL, Mak RH
J Clin Invest. 2005 115 (6): 1659-65

PMID: 15931394 · PMCID: PMC1136984 · DOI:10.1172/JCI22521

The pathogenesis of cachexia in patients with uremia is unknown. We tested the hypothesis that uremia-associated cachexia is caused by leptin signaling through the hypothalamic melanocortin receptor 4 (MC4-R). We performed either subtotal nephrectomy (N) or sham operations in WT, leptin receptor-deficient (db/db), and MC4-R knockout (MC4-RKO) mice. The animals were on 17% protein diets, and none of the uremic animals were acidotic. WT-N mice produced a classic syndrome of cachexia characterized by decreased food intake, increased metabolic rate, and loss of lean body mass. Corrected leptin levels were elevated. db/db mice and MC4-RKO mice resisted the cachexic effects of uremia on weight gain, body composition, and metabolic rate. Likewise, treatment of WT mice with intracranial agouti-related peptide reversed the cachexic effects of uremia on appetite, weight gain, body composition, and metabolic rate. Gene expression of ubiquitin C and proteasome subunits C2, C3, and C9 was not changed in the uremic animals, suggesting that other pathways are involved in this model of nonacidotic uremic cachexia. The results of this study suggest that elevated circulating levels of cytokines such as leptin may be an important cause of uremia-associated cachexia via signaling through the central melanocortin system.

MeSH Terms (18)

Agouti-Related Protein Animals Body Weight Cachexia Eating Gene Expression Regulation Humans Leptin Mice Mice, Knockout Peptide Fragments Proteasome Endopeptidase Complex Receptor, Melanocortin, Type 4 Receptors, Cell Surface Receptors, Leptin Signal Transduction Ubiquitin C Uremia

Connections (1)

This publication is referenced by other Labnodes entities: