Baldwin B A, de la Riva C, Gerskowitch V P
AFRC Institute of Animal Physiology and Genetics Research, Cambridge Research Station, Babraham, UK.
Physiol Behav. 1994 Jan;55(1):175-9. doi: 10.1016/0031-9384(94)90027-2.
The effect of a novel CCKA receptor antagonist 2-naphthalene sulphonyl-L-aspartyl-2-(phenethyl)amide, sodium salt (2-NAP) on the reduction of food intake induced by exogenous CCK, administered centrally or peripherally, has been examined in pigs. 2-NAP is hydrophilic and should not readily cross the blood-brain barrier. Intravenous (IV) 2-NAP (20 or 40 mg/kg) injected prior to IV CCK-8S (1 microgram/kg) abolished the inhibitory effect of CCK-8S on operant food intake in hungry pigs. Intravenous injections of 2-NAP (20 and 30 mg/kg) prior to the administration of intracerebroventricular (ICV) injection of CCK-8S (1 microgram) did not affect the inhibitory action of ICV CCK-8S on food intake. ICV injection of 2-NAP (5 mg) abolished the inhibitory effect on food intake of ICV CCK-8S (1 microgram). The results indicate that 2-NAP does not cross the blood-brain barrier readily and that central and peripheral administration of CCK-8S inhibits feeding by different mechanisms. Neither ICV nor IV injection of 2-NAP altered food intake when injected alone.
在猪身上研究了一种新型胆囊收缩素A(CCKA)受体拮抗剂2-萘磺酰-L-天冬氨酰-2-(苯乙基)酰胺钠盐(2-NAP)对外源性CCK经中枢或外周给药诱导的食物摄入量减少的影响。2-NAP具有亲水性,不易穿过血脑屏障。在静脉注射CCK-8S(1微克/千克)之前静脉注射2-NAP(20或40毫克/千克)可消除CCK-8S对饥饿猪操作性食物摄入量的抑制作用。在脑室内注射CCK-8S(1微克)之前静脉注射2-NAP(20和30毫克/千克)并不影响脑室内CCK-8S对食物摄入量的抑制作用。脑室内注射2-NAP(5毫克)可消除脑室内CCK-8S(1微克)对食物摄入量的抑制作用。结果表明,2-NAP不易穿过血脑屏障,并且CCK-8S经中枢和外周给药通过不同机制抑制进食。单独注射时,脑室内或静脉注射2-NAP均未改变食物摄入量。