Rakovska A, Milenov K, Henklein P
Institute of Physiology, Bulgarian Academy of Sciences, Sofia.
Experientia. 1990 Oct 15;46(10):1037-41. doi: 10.1007/BF01940666.
Suc-Tyr-(SE)-Met-Gly-Trp-Met-Asp-beta-phenethylamide (GE 410) competitively antagonized the contractions of smooth muscle strips from guinea pig ileum (pA2 = 7.6, n = 0.95) induced by cholecystokinin-octapeptide (CCK8). GE 410 inhibited the electrically-induced cholinergically mediated contractile responses and the [3H]ACh release in the ileum, as well as the CCK-stimulated electrical contractile responses and the [3H]ACh release in the cholinergic nerve terminals. The results suggest the existence of CCK-receptors not only in the smooth muscles but also on the neurons.
琥珀酰 - 酪氨酸 -(琥珀酰 - 乙基)- 蛋氨酸 - 甘氨酸 - 色氨酸 - 蛋氨酸 - 天冬氨酸 -β-苯乙酰胺(GE 410)竞争性拮抗胆囊收缩素八肽(CCK8)诱导的豚鼠回肠平滑肌条收缩(pA2 = 7.6,n = 0.95)。GE 410抑制回肠中电诱导的胆碱能介导的收缩反应以及[3H]乙酰胆碱释放,以及CCK刺激的胆碱能神经末梢中的电收缩反应和[3H]乙酰胆碱释放。结果表明不仅在平滑肌中而且在神经元上都存在CCK受体。