Ennis C, Janssen P A, Schnieden H, Cox B
J Pharm Pharmacol. 1979 Apr;31(4):217-21. doi: 10.1111/j.2042-7158.1979.tb13482.x.
Dopamine, apomorphine, noradrenaline and isoprenaline reduced the response of the isolated guinea-pig ileum to exogenous acetylcholine by a maximum of 40%. Propranolol reversed this inhibition whilst phentolamine and pimozide were ineffective, suggesting that the drugs were acting on a post-synaptic beta-adrenoceptor. The same agonists were more effective as inhibitors of the response to transmural electrical stimulation of the ileum, lower doses producing almost complete inhibition. This inhibition was partially antagonized by phentolamine, pimozide and propranolol. Clonidine proved to be the most potent inhibitor of the response to transmural electrical stimulation, whilst phenylephrine was ineffective. pA2 determinations showed that phentolamine was a potent antagonist of clonidine but a weak antagonist of apomorphine whilst for pimozide the opposite was true. The results suggest that there are two populations of prejunctional receptors on the cholinergic nerves innervating the smooth muscle of the guinea-pig ileum. One receptor is similar to a classical prejunctional alpha-adrenoceptor and the other resembles a central dopamine receptor.
多巴胺、阿扑吗啡、去甲肾上腺素和异丙肾上腺素使离体豚鼠回肠对外源性乙酰胆碱的反应最大降低了40%。普萘洛尔可逆转这种抑制作用,而酚妥拉明和匹莫齐特则无效,这表明这些药物作用于突触后β - 肾上腺素能受体。相同的激动剂作为回肠跨壁电刺激反应的抑制剂更有效,较低剂量就能产生几乎完全的抑制作用。这种抑制作用可被酚妥拉明、匹莫齐特和普萘洛尔部分拮抗。可乐定被证明是对跨壁电刺激反应最有效的抑制剂,而去氧肾上腺素则无效。pA2测定表明,酚妥拉明是可乐定的强效拮抗剂,但对阿扑吗啡是弱拮抗剂,而匹莫齐特则相反。结果表明,支配豚鼠回肠平滑肌的胆碱能神经上存在两类节前受体。一种受体类似于经典的节前α - 肾上腺素能受体,另一种类似于中枢多巴胺受体。