膜兴奋性修饰药物对achatin- 1引起的兴奋的影响

Divina E. Santos, Hiroshi Takeuchi
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引用次数: 0

摘要

1. 气压喷射一种内源性四肽,含有d-苯基丙氨酸残基的Achatina - i (gly -d- phel - ala -l- asp),在非洲大蜗牛Achatina fulica f russac的可识别的巨大神经元PON(周期性振荡神经元)中产生向内电流(Iin)。在电压箝位下,观察灌注膜兴奋性修饰药物对achatin-I引起的PON兴奋的影响。4种通道阻断药物河豚毒素(TTX)、四乙基氯化铵(TEA)、异拉帕米和微毒素在10、−4 M时对肽引起的PON兴奋无显著影响。膜超极化剂N-β-苯基丙炔- l-酪氨酸(BPLT)在10−6 M和改变l-谷氨酸反应的豆豆蛋白a (Con a)在100 μgml−1时被认为几乎不影响紫菜素- 1引起的PON兴奋。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Influence of the drugs for membrane excitability modification on the excitation caused by achatin-I

1. The pneumatic pressure ejection of achatin-I (Gly-d-Phe-l-Ala-l-Asp), an endogenous tetrapeptide having a d-phenylalanine residue, produced an inward current (Iin) in an identifiable giant neuron, PON (periodically oscillating neuron), of an African giant snail, Achatina fulica Férussac. The influence of the drugs for membrane excitability modification, applied by perfusion, on the PON excitation caused by achatin-I was examined under voltage clamp.

2. The four channel blocking drugs, tetrodotoxin (TTX), tetraethylammonium chloride (TEA), verapamil and picrotoxin, at 10,−4 M did not affect significantly the PON excitation caused by the peptide.

3. N-β-phenylpropionyl-L-tyrosine (BPLT), a membrane hyperpolarizant, at 10−6 M and concanavalin A (Con A), which altered the response to l-glutamate, at 100 μgml−1 were considered to hardly influence the PON excitation caused by achatin-I.

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