Endogenous ACTH, not only {alpha}-melanocyte-stimulating hormone, reduces food intake mediated by hypothalamic mechanisms

1 Department of Internal Medicine I, Luebeck University, Luebeck; 2 General Hospital Stuttgart - Buergerhospital, Department of Endocrinology, Diabetology and Geriatrics, Stuttgart, Germany; and 3 Department of Physiology, School of Medicine, University of California, San Francisco, California Submitted 25 June 2009 ; accepted in final form 10 November 2009 ACTH and -melanocyte-stimulating hormone ( -MSH) are both consecutively processed from proopiomelanocortin (POMC), which is synthesized in hypothalamic arcuate neurons innervating the paraventricular nuclei (PVN). POMC secretion/synthesis is regulated by energy availability. ACTH and -MSH bind with equal affinity to melanocortin-4 receptors and elicit similar effects on signal transduction in-vitro. Endogenous -MSH thus far is believed to be the major physiological agonist and to act in an anorexigenic manner. Until now, it was fully unknown whether endogenous ACTH is also involved in the regulation of appetite and food intake. In this study in rats, we now show that icv ACTH as well as -MSH possess anorexigenic effects in the PVN or areas in close proximity in vivo and that the effect of ACTH is direct and not mediated via -MSH. We investigated the roles of endogenous ACTH and -MSH by PVN application of the respective antibodies under different physiological conditions. In satiated rats with high levels of ACTH and -MSH in the PVN, antibody administration increased food intake and body weight gain; hungry animals were unaffected. Finally, repeated injections of ACTH antibodies into PVN resulted in persistently increased food intake during the light period. These data now provide robust evidence that endogenous ACTH without further processing acts in the PVN or areas in close proximity to reduce food intake under conditions of feeding-induced satiety. adrenocorticotropic hormone; appetite; hypothalamus; paraventricular nucleus; melanocortin-4 receptor Address for reprint requests and other correspondence: C. Schulz, Dept. of Internal Medicine I, Luebeck Univ., Ratzeburger Allee 160, 23538 Luebeck, Germany (E-mail: carla.schulz{at}uk-sh.de ).