Different Influence of CGRP(8-37), an Amylin and CGRP Antagonist, on the Anorectic Effects of Cholecystokinin and Bombesin in Diabetic and Normal Rats

Abstract

Lutz, T. A., T. R. Pieber, B. Walzer, E. Del Prete and E. Scharrer. Different influence of CGRP(8-37), an amylin and CGRP antagonist, on the anorectic effects of cholecystokinin and bombesin in diabetic and normal rats. Peptides 18(5) 643-649, 1997.—Because previous studies had suggested that the anorectic effects of cholecystokinin (CCK) and bombesin (BBS) depend partly on the release of amylin or calcitonin gene-related peptide (CGRP), we investigated the influence of the amylin and CGRP receptor antagonist CGRP(8-37) on the anorectic effects of CCK and BBS in streptozotocin (STZ)-diabetic and nondiabetic rats. STZ-diabetic rats had significantly lower plasma amylin and insulin concentrations than nondiabetic control rats. Amylin (5 μg/kg or 2.5 μg/rat) injected IP at dark onset after 24-h food deprivation elicited an anorectic effect of similar extent in STZ-diabetic and control rats. Under similar conditions, CCK (0.25 and 2 μg/kg) and BBS (5 μg/kg) reduced food intake in both STZ-diabetic and nondiabetic rats. These effects were markedly attenuated by CGRP(8-37) (10 μg/kg) in nondiabetics but not in STZ-diabetic rats. It is concluded that part of the anorectic effects of CCK and BBS depend on the release of amylin from pancreatic B-cells.