Ohizumi Y, Shibata S, Tachibana K
J Pharmacol Exp Ther. 1981 May;217(2):475-80.
Ciguatoxin (CTX), one of the most potent known toxic substances among marine toxins, causes a contraction in the isolated guinea-pig vas deferens at the concentration of above 3 x 10(-7) g/ml. The CTX-induced contraction of the vas deferens was inhibited or abolished by a treatment with phentolamine or guanethidine, but not affected in the presence of atropine or mecamylamine. Furthermore, this contraction was blocked by a treatment with tetrodotoxin, procaine or cold storage and incubation in a low Na+ medium. On the other hand, CTX markedly potentiated the contraction of vas deferens which was induced by norepinephrine (NE), acetylcholine or high-K, whereas it inhibited the contractile response to transmural stimulation. CTX caused a marked release of NE from the adrenergic nerves, which was blocked after treatment with tetrodotoxin or incubation in a Ca-free medium. On the basis of these results, it is suggested that the CTX-induced contraction is the result of an indirect action mediated through the NE release from the adrenergic nerve terminals and that the effect of NE released from the presynaptic sites is potentiated by CTX at the postsynaptic sites. The inhibitory effect of CTX on the contractile response to transmural stimulation may be due to decreasing the transmitter release caused by stimulation.
雪卡毒素(CTX)是海洋毒素中已知毒性最强的物质之一,在浓度高于3×10⁻⁷克/毫升时可使离体豚鼠输精管收缩。酚妥拉明或胍乙啶处理可抑制或消除CTX诱导的输精管收缩,但阿托品或美加明存在时则无影响。此外,河豚毒素、普鲁卡因处理或在低钠培养基中冷藏及孵育可阻断这种收缩。另一方面,CTX显著增强去甲肾上腺素(NE)、乙酰胆碱或高钾诱导的输精管收缩,而抑制对跨壁刺激的收缩反应。CTX可使肾上腺素能神经显著释放NE,河豚毒素处理或在无钙培养基中孵育后这种释放被阻断。基于这些结果,提示CTX诱导的收缩是通过肾上腺素能神经末梢释放NE介导的间接作用的结果,且CTX在突触后位点增强了突触前位点释放的NE的作用。CTX对跨壁刺激收缩反应的抑制作用可能是由于减少了刺激引起的递质释放。