Activation of central neuropeptide Y Y1 receptors potently stimulates food intake in male rhesus monkeys

• Published in: The journal of clinical endocrinology and metabolism 1999-10, Vol.84 (10), p.3781-3791
• Main Authors: LARSEN, P. J, TANG-CHRISTENSEN, M, STIDSEN, C. E, MADSEN, K, SMITH, M. S, CAMERON, J. L
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; Brain - metabolism; Clonidine - pharmacology; Dose-Response Relationship, Drug; Eating - drug effects; Eating - physiology; Feeding. Feeding behavior; Fundamental and applied biological sciences. Psychology; Hydrocortisone - blood; Injections, Intraventricular; Insulin - blood; Macaca mulatta; Male; Neuropeptide Y - agonists; Neuropeptide Y - antagonists & inhibitors; Neuropeptide Y - pharmacology; Peptides, Cyclic - pharmacology; Receptors, Neuropeptide Y - antagonists & inhibitors; Receptors, Neuropeptide Y - physiology; Vertebrates: anatomy and physiology, studies on body, several organs or systems
• ISSN: 0021-972X; 1945-7197
• DOI: 10.1210/jc.84.10.3781

The orexigenic role of central neuropeptide Y (NPY) in nonhuman primates has been questioned. Therefore, we have studied the effect of central NPY on feeding in ad libitum-fed male rhesus macaques. NPY dose-dependently increased food intake, with the maximal effect obtained by 50 microg (960 min food intake +/- SEM, 104 +/- 5 to 188 +/- 11 g; vehicle vs. NPY; n = 6). Blood glucose levels were unaffected by intracerebroventricular administration of NPY, but animals receiving either 20 or 50 microg displayed increased plasma levels of insulin and cortisol at few time points. To assess the pharmacological specificity of this response, a novel Y1 antagonist, [(Ile,Glu,Pro,Daba,Tyr,Arg,Leu,Arg,Tyr-NH2)2 cyclic (2,4'),(2',4)-diamide] (Y1ANT), was synthesized. Receptor binding experiments demonstrated that Y1ANT preferentially binds to Y1 and Y4 receptors (pKi 10.12 +/- 0.06 and 9.11 +/- 0.05 nmol/L, respectively). Functional analysis revealed that Y1ANT is a Y1 antagonist and a partial Y4 agonist. Central administration of Y1ANT blocked NPY-induced feeding. In food-deprived monkeys, Y1ANT attenuated the feeding response. However, Y1ANT had no effect on food intake in satiated monkeys. Thus, endogenous NPY is likely to be involved in the regulation of food intake in the nonhuman primate, and this effect is at least partially mediated via Y1-like receptors.