Hecker S E, Mitchelson F
J Pharm Pharmacol. 1976 May;28(5):441-6. doi: 10.1111/j.2042-7158.1976.tb04651.x.
The effect of hemicholinium-3 (HC-3) on responses of the rat isolated bladder and ileum to acetylcholine and carbachol was investigated in the absence and presence of a number of anticholinesterases. Responses of the bladder to acetylcholine were potentiated by DFP, edrophonium, BW284C51 and physostigmine but were unaffected by the specific butyrylcholinesterase inhibitor iso-OMPA. Responses to carbachol were not potentiated by the anticholinesterases. HC-3 (1.7 X 10(-4) M) inhibited responses to carbachol without affecting those to acetylcholine. In the presence of physostigmine or DFP responses to acetylcholine were inhibited by HC-3 but no such inhibition was observed in the presence of BW284C51, edrophonium or iso-OMPA or a combination of the latter two anticholinesterases. Responses to carbachol were also inhibited to a greater extent in the presence of DFP. In the ileum, responses to acetylcholine were increased in the presence of DFP, edrophonium and physostigmine but were unaffected by iso-Ompa. responses to carbachol were not increased by any of the anticholinesterases. HC-3 (2.8 X 10(-4) M) inhibited responses to both acetylcholine and carbachol in the ileum and the degree of inhibition was not significantly altered by the presence of any of the anticholinesterases used. Although a weak anticholinesterase, HC-3 was also found to decrease the inhibitory action of physostigmine on the hydrolysis of acetylcholine by homogenates of rat ileum. A similar effect was noted with DFP but not with edrophonium. The results obtained do not support a prejunctional action for HC-3 in antagonizing responses to carbachol. It is concluded that in addition to an inhibitory action on the post-junctional muscarinic receptor HC-3 may interfere with the anticholinesterase activity of some cholinesterase inhibitors such as physostigmine and DFP but not edrophonium.
在存在和不存在多种抗胆碱酯酶的情况下,研究了半胱氨酸-3(HC-3)对大鼠离体膀胱和回肠对乙酰胆碱和卡巴胆碱反应的影响。膀胱对乙酰胆碱的反应在二异丙基氟磷酸酯(DFP)、依酚氯铵、BW284C51和毒扁豆碱存在时增强,但不受特异性丁酰胆碱酯酶抑制剂异-OMPA的影响。抗胆碱酯酶未增强对卡巴胆碱的反应。HC-3(1.7×10⁻⁴ M)抑制对卡巴胆碱的反应,而不影响对乙酰胆碱的反应。在毒扁豆碱或DFP存在时,HC-3抑制对乙酰胆碱的反应,但在BW284C51、依酚氯铵或异-OMPA或后两种抗胆碱酯酶的组合存在时未观察到这种抑制作用。在DFP存在时,对卡巴胆碱的反应也受到更大程度的抑制。在回肠中,在DFP、依酚氯铵和毒扁豆碱存在时,对乙酰胆碱的反应增强,但不受异-Ompa的影响。抗胆碱酯酶均未增强对卡巴胆碱的反应。HC-3(2.8×10⁻⁴ M)抑制回肠中对乙酰胆碱和卡巴胆碱的反应,并且所用任何抗胆碱酯酶的存在均未显著改变抑制程度。尽管HC-3是一种弱抗胆碱酯酶,但还发现它可降低毒扁豆碱对大鼠回肠匀浆水解乙酰胆碱的抑制作用。DFP也有类似作用,但依酚氯铵没有。所得结果不支持HC-3在拮抗对卡巴胆碱的反应中有节前作用。结论是,除了对节后毒蕈碱受体有抑制作用外,HC-3可能会干扰某些胆碱酯酶抑制剂如毒扁豆碱和DFP的抗胆碱酯酶活性,但不干扰依酚氯铵的活性。