Sakatani N, Inui A, Baba S
Second Department of Internal Medicine, School of Medicine, Kobe University, Japan.
Nihon Naibunpi Gakkai Zasshi. 1989 Oct 20;65(10):1149-58. doi: 10.1507/endocrine1927.65.10_1149.
We administered two cholecystokinin antagonists to dogs intravenously (i.v.) and into the third cerebral ventricle (i.t.v.). Proglumide (3-300mg/kg/hr i.v. or 0.1-10mg/dog i.t.v.) reversed the satiety previously shown by mongrel dogs after i.t.v. CCK-8. A new glutaramic derivative, CR1409, blocked this satiety even more strongly when administered by either route. Proglumide increased proglumide levels in ventricular fluid, indicating its ability to cross the blood-brain barrier. However, i.t.v. proglumide did not appear in the blood during the observation period. These results suggest that systemic proglumide and CR1409 act as antagonists of the central CCK receptor concerning satiety in dogs; intravenously administered proglumide was found to cross the blood-brain barrier and partially but significantly reverse the satiety caused by CCK-8.
我们给狗静脉注射(i.v.)和脑室内注射(i.t.v.)两种胆囊收缩素拮抗剂。丙谷胺(静脉注射3 - 300mg/kg/小时或脑室内注射0.1 - 10mg/只狗)可逆转杂种狗在脑室内注射CCK - 8后先前出现的饱腹感。一种新的谷氨酸衍生物CR1409,通过任何一种途径给药时,对这种饱腹感的阻断作用更强。丙谷胺可提高脑室液中丙谷胺的水平,表明其能够穿过血脑屏障。然而,在观察期内,脑室内注射的丙谷胺并未出现在血液中。这些结果表明,全身应用丙谷胺和CR1409作为犬饱腹感相关中枢CCK受体的拮抗剂;发现静脉注射的丙谷胺可穿过血脑屏障,并部分但显著地逆转CCK - 8引起的饱腹感。