Ribeiro J A, Sebastião A M
Br J Pharmacol. 1984 Feb;81(2):277-82. doi: 10.1111/j.1476-5381.1984.tb10075.x.
The effects of adenosine triphosphate (ATP), adenosine diphosphate (ADP), adenosine monophosphate (AMP), and adenosine on compound action potentials were investigated in de-sheathed frog-sciatic nerve preparations. ATP and ADP but not adenosine antagonized the inhibitory action of tetrodotoxin (TTX) on nerve conduction. AMP had little or no antagonistic effect on TTX-induced axonal block. ATP was more effective than ADP. The effects of the nucleotides were related to the degree of the TTX-induced inhibition and were more evident where the blockade was more intense. ATP and ADP but not adenosine antagonized the procaine-induced axonal blockade which, in some experiments, was completely reversed by these nucleotides. ATP and ADP were of similar potency. The axonal blockade induced by pentobarbitone was not antagonized by ATP, ADP, AMP or adenosine. The possibility that ATP stimulates a TTX-sensitive sodium channel is discussed.
在去鞘的蛙坐骨神经标本中,研究了三磷酸腺苷(ATP)、二磷酸腺苷(ADP)、一磷酸腺苷(AMP)和腺苷对复合动作电位的影响。ATP和ADP而非腺苷拮抗了河豚毒素(TTX)对神经传导的抑制作用。AMP对TTX诱导的轴突阻滞几乎没有或没有拮抗作用。ATP比ADP更有效。核苷酸的作用与TTX诱导的抑制程度有关,在阻滞更强烈的地方更明显。ATP和ADP而非腺苷拮抗了普鲁卡因诱导的轴突阻滞,在一些实验中,这些核苷酸完全逆转了这种阻滞。ATP和ADP具有相似的效力。戊巴比妥诱导的轴突阻滞未被ATP、ADP、AMP或腺苷拮抗。讨论了ATP刺激TTX敏感钠通道的可能性。