Katsuragi T, Furukawa T
J Pharm Pharmacol. 1979 Dec;31(12):822-5. doi: 10.1111/j.2042-7158.1979.tb13673.x.
Methysergide (3 x 10(-6) M) enhanced the contractile responses of the isolated stripped vas deferens of guinea-pig to acetylchline(ACh) and arecoline, but not those to noradrenaline, tyramine and bradykinin. Methysergide (3 x 10(-5) M) suppressed the contraction elicited by noradrenaline or histamine. The methysergide-induced potentiation of the response to ACh was prevented by pre-addition of hemicholinium but not by tetrodotoxin or morphine. The augmentation of the response to ACh by physostigmine was unaffected by hemicholinium. The phasic contraction of the tissue elicited by 30 mM KCl was also enhanced by methysergide, and this enhancement was prevented by the pre-addition of atropine (1.4 x 10(-7) M). In the depolarized vas deferens after exposure to 30 mM KCl, methysergide occasionally induced a sustained tonic contraction which was inhibited by atropine. These findings suggest that methysergide facilitates a release of ACh by acting on the cholinergic nerve terminals and selectively potentiates the cholinergic response.
甲基麦角新碱(3×10⁻⁶M)增强了豚鼠离体输精管对乙酰胆碱(ACh)和槟榔碱的收缩反应,但对去甲肾上腺素、酪胺和缓激肽的收缩反应无增强作用。甲基麦角新碱(3×10⁻⁵M)抑制了去甲肾上腺素或组胺引起的收缩。预先加入半胱氨酸可阻止甲基麦角新碱诱导的对ACh反应的增强,但河豚毒素或吗啡则不能。毒扁豆碱对ACh反应的增强不受半胱氨酸的影响。30mM氯化钾引起的组织相性收缩也被甲基麦角新碱增强,预先加入阿托品(1.4×10⁻⁷M)可阻止这种增强。在暴露于30mM氯化钾后去极化的输精管中,甲基麦角新碱偶尔会诱导持续的强直性收缩,这种收缩被阿托品抑制。这些发现表明,甲基麦角新碱通过作用于胆碱能神经末梢促进ACh的释放,并选择性地增强胆碱能反应。