CHOLECYSTOKININ-OCTAPEPTIDE ANALOGS SUPPRESS FOOD-INTAKE VIA CENTRAL CCK-A RECEPTORS IN MICE

To examine the mechanism of the satiety-producing effect of cholecysto kinin (CCK) in the central nervous system, we compared the potency of intraperitoneally (ip) or intracerebroventricularly (icv) administered CCK-8 and its analogues on food intake in fasted mice. The icv admini stration of a small dose of CCK-8 (0.03 nmol/brain) or of Suc-(Thr28, Leu29, MePhe 33)-CCK-7 (0.001 nmol/brain) suppressed food intake for 2 0 min, whereas CCK-8 (1 nmol/kg, which is equivalent to 0.03 nmol/brai n) or Suc-(Thr28, Leu29, MePhe33)-CCK-7 1 nmol/kg) had satiety effect after ip administration. Dose-response studies indicated the following rank order of potency: Suc-CCK-7 greater-than-or-equal-to Suc-(Thr28, Leu29, MePhe33)-CCK-7 greater-than-or-equal-to CCK-8 greater-than-or- equal-to (Nle28,31) -CCK-8 >> desulfated CCK-8 = CCK-4 = 0 in the case of ip administration and Suc-(Thr28, Leu29, Me-Phe33)-CCK-7 >> Suc-CC K-7 greater-than-or-equal-to CCK-8 greater-than-or-equal-to (Nle28,31) -CCK-8 >> desulfated CCK-8 = CCK-4 = 0 in the case of icv administrati on. The selective CCK-A receptor antagonist MK-329 reversed the inhibi tory effect of the centrally as well as peripherally administered CCK- 8, or of Suc-(Thr28, Leu29, MePhe33)-CCK-7, whereas the selective CCK- B receptor antagonist L-365260 did not. The icv administered CCK-8 did not appear in the peripheral circulation. These findings suggest the participation of CCK-A receptors in the brain in mediating the satiety effect of CCK and the difference in CCK-A receptors in the brain and peripheral tissues.