Fukamauchi F, Yoshikawa T, Kaneno S, Shibuya H, Takahashi R
Department of Neuropsychiatry, Faculty of Medicine, Tokyo Medical and Dental University, Japan.
Neuropeptides. 1987 Oct;10(3):221-5. doi: 10.1016/0143-4179(87)90071-0.
The specific cholecystokinin (CCK) binding in the slide-mounted tissue sections of the rat frontal cortex was measured with [3H]-CCK-8. The binding was saturable, reversible, high in affinity, and inhibited by caerulein. The chronic administration of dopamine (DA) antagonists and methamphetamine (MAP) showed a tendency to increase the [3H]-CCK-8 binding sites (Bmax) in the frontal cortex. Long-term treatments with DA antagonists led to the depletion of CCK-8 and may have caused an observed proliferation of CCK-8 receptors in the frontal cortex.
采用[3H]-CCK-8测定大鼠额叶皮质冰冻切片组织中的特异性胆囊收缩素(CCK)结合情况。该结合具有饱和性、可逆性、高亲和力,且可被雨蛙素抑制。长期给予多巴胺(DA)拮抗剂和甲基苯丙胺(MAP)显示出增加额叶皮质中[3H]-CCK-8结合位点(Bmax)的趋势。长期使用DA拮抗剂导致CCK-8耗竭,并可能致使额叶皮质中观察到的CCK-8受体增殖。