Widman M, Rosin D, Dewey W L
J Pharmacol Exp Ther. 1978 May;205(2):311-8.
The antinociceptive effect of intracerebroventricularly administered acetylcholine as measured in the mouse tail-flick test was reduced by intracerebroventricularly injected calcium, magnesium and manganese. Maximum antagonism of acetylcholine-induced antinociception was observed with a 1-hour calcium pretreatment. Significant reduction existed at 2- but not 4-hour pretreatment. Barium and strontium were inactive. The antinociceptive effect of acetylcholine was potentiated by lanthanum and ethylene glycol tetraacetic acid but not by ethylenediamine tetraacetic acid. The ionophore A23187 was shown to increase greatly the antagonistic effect of a low dose of calcium. The ionophore alone did not significantly alter the effect of acetylcholine. Thus, it appears that calcium must penetrate cell membranes to reduce the effect of acetylcholine. In addition to acetylcholine, it was found that the antinociceptive effects of oxotremorine and physostigmine could also be reduced by calcium. These data indicate that alterations in intracellular calcium are involved in cholinergically induced antinociception.
在小鼠甩尾试验中所测定的脑室内注射乙酰胆碱的抗伤害感受作用,被脑室内注射的钙、镁和锰降低。在进行1小时的钙预处理时,观察到乙酰胆碱诱导的抗伤害感受作用出现最大程度的拮抗。在进行2小时而非4小时的预处理时,存在显著的降低。钡和锶没有活性。乙酰胆碱的抗伤害感受作用被镧和乙二醇四乙酸增强,但未被乙二胺四乙酸增强。离子载体A23187被证明能极大地增强低剂量钙的拮抗作用。单独的离子载体不会显著改变乙酰胆碱的作用。因此,似乎钙必须穿透细胞膜才能降低乙酰胆碱的作用。除了乙酰胆碱外,还发现氧化震颤素和毒扁豆碱的抗伤害感受作用也能被钙降低。这些数据表明细胞内钙的改变参与了胆碱能诱导的抗伤害感受作用。