Salimi M, Khoyi M A, Dibai M A
Jpn J Pharmacol. 1979 Apr;29(2):151-60. doi: 10.1254/jjp.29.151.
The effect of ethacrynic acid on the motor function of guinea pig ileum was studied in vitro. Ethacrynic acid produced dose-related (5-160 microgram/ml) contractions in this tissue. Morphine, tetrodotoxin and sodium-free medium prevented the contractions while hexamethonium, diphenhydramine, methysergide or indomethacin did not. Atropine in a high concentration (0.1 microgram/ml) only inhibited the contractions. Ethacrynic acid inhibited the contraction of ileum induced by electrical stimulation of intramural nerves. This was not prevented by pretreatment with reserpine. Repeated exposure to ethyacrynic acid developed tachyphylaxis in contractile response. Inhibition of electrically elicited contraction of guinea pig ileum also diminished with repeated treatment. Ethacrynic acid (80-160 micrograms/ml) inhibited the peristaltic reflex of the guinea pig ileum. It is concluded that the excitatory effect of ethacrynic acid is most probably mediated by the release of neurotransmitter, however, the mechanism of the inhibitory effect remains to be elucidated.
在体外研究了依他尼酸对豚鼠回肠运动功能的影响。依他尼酸在该组织中产生剂量相关(5 - 160微克/毫升)的收缩。吗啡、河豚毒素和无钠培养基可阻止收缩,而六甲铵、苯海拉明、甲基麦角新碱或吲哚美辛则不能。高浓度(0.1微克/毫升)的阿托品仅抑制收缩。依他尼酸抑制由壁内神经电刺激诱导的回肠收缩。利血平预处理不能阻止这种作用。反复暴露于依他尼酸会使收缩反应产生快速耐受性。反复处理后,对豚鼠回肠电诱发收缩的抑制作用也会减弱。依他尼酸(80 - 160微克/毫升)抑制豚鼠回肠的蠕动反射。结论是,依他尼酸的兴奋作用很可能是通过神经递质的释放介导的,然而,其抑制作用的机制仍有待阐明。