Selective melanocortin MC4 receptor blockage reduces immobilization stress-induced anorexia in rats.

We investigated the effects of selective melanocortin MC4 receptor blockage on immobilization stress-induced anorexia. Male rats were subjected to immobilization once a day for 4 days. Prior to each of the stress treatments, the rats were injected i.c.v. (intracerebroventricularly) with either saline or the melanocortin MC4 receptor antagonist HS014 (cyclic [AcCys11, D-Nal14, Cys18, Asp-(NH22)2]beta-MSH-(11-22) (melanocyte-stimulating hormone). Rats subjected to neither stress nor i.c.v. injections served as controls. The results showed that the cumulative food intake and body weight gain in the stressed group treated with HS014 was significantly higher than in the stressed group and significantly lower than in the control group. Repeated injections of the melanocortin MC4 receptor antagonist were effective and there were no signs of tachyphylaxis. This is the first report showing that melanocortin MC4 receptor blockage can relieve an anorectic condition, which may indicate that melanocortin MC4 receptor blockage is an effective way to treat anorectic disorders.

[1]  A. Vergoni,et al.  Corticotropin inhibits food intake in rats , 1986, Neuropeptides.

[2]  J. Wikberg,et al.  Differential influence of a selective melanocortin MC4 receptor antagonist (HS014) on melanocortin-induced behavioral effects in rats. , 1998, European journal of pharmacology.

[3]  J. Wikberg,et al.  Selective antagonist for the melanocortin 4 receptor (HS014) increases food intake in free-feeding rats. , 1998, Biochemical and biophysical research communications.

[4]  R. Adan,et al.  The role of central melanocortin receptors in the activation of the hypothalamus‐pituitary‐adrenal‐axis and the induction of excessive grooming , 1998, British journal of pharmacology.

[5]  S. Carr,et al.  Orexins and Orexin Receptors: A Family of Hypothalamic Neuropeptides and G Protein-Coupled Receptors that Regulate Feeding Behavior , 1998, Cell.

[6]  J. Wikberg,et al.  Evidence for involvement of the melanocortin MC4 receptor in the effects of leptin on food intake and body weight. , 1998, European journal of pharmacology.

[7]  V. Hruby,et al.  Potent and prolonged acting cyclic lactam analogues of alpha-melanotropin: design based on molecular dynamics. , 1989, Journal of medicinal chemistry.

[8]  R. Cone,et al.  Targeted Disruption of the Melanocortin-4 Receptor Results in Obesity in Mice , 1997, Cell.

[9]  G. Paxinos,et al.  The Rat Brain in Stereotaxic Coordinates , 1983 .

[10]  R. Seeley,et al.  Melanocortin receptors in leptin effects , 1997, Nature.

[11]  R. Cone,et al.  Cyclic lactam alpha-melanotropin analogues of Ac-Nle4-cyclo[Asp5, D-Phe7,Lys10] alpha-melanocyte-stimulating hormone-(4-10)-NH2 with bulky aromatic amino acids at position 7 show high antagonist potency and selectivity at specific melanocortin receptors. , 1995, Journal of medicinal chemistry.

[12]  A. Eberle The Melanotropins: Chemistry, Physiology and Mechanisms of Action , 1988 .

[13]  P. J. Larsen,et al.  Hypothalamic CART is a new anorectic peptide regulated by leptin , 1998, Nature.

[14]  R. Adan,et al.  Brain Melanocortin Receptors: From Cloning to Function , 1997, Peptides.

[15]  P. Prusis,et al.  Selectivity of Cyclic [d-Nal7] and [d-Phe7] Substituted MSH Analogues for the Melanocortin Receptor Subtypes , 1997, Peptides.

[16]  S. Gaillet,et al.  Central Regulation of ACTH Release in Stress a , 1995, Annals of the New York Academy of Sciences.

[17]  J. Wikberg,et al.  Evidence that orexigenic effects of melanocortin 4 receptor antagonist HS014 are mediated by neuropeptide Y. , 1998, Biochemical and biophysical research communications.

[18]  P. Prusis,et al.  Discovery of novel melanocortin4 receptor selective MSH analogues , 1998, British journal of pharmacology.

[19]  J. Wikberg,et al.  Characterisation of the melanocortin 4 receptor by radioligand binding. , 1996, Pharmacology & toxicology.

[20]  A. Vergoni,et al.  ACTH-(1–24) and α-MSH antagonize feeding behavior stimulated by kappa opiate agonists , 1986, Peptides.