Youssef S A, Ramadan A, Afifi N A, Aziz M D
Department of Pharmacology, Faculty of Veterinary Medicine, Cairo University, Giza, Egypt.
Dtsch Tierarztl Wochenschr. 1991 Jun;98(6):213-6.
The effect of sodium taurocholate (S. T.) on the contractile response of rat-phrenic nerve diaphragm, frog's musculus rectus abdominis and frog's musculus gastrocnemius sciatic nerve preparation was studied. Moreover, interaction of S. T. with neuromuscular blockers are carried out, too. S. T. was found to have a dose-dependent reduction in the contractile response of the tested preparation. On the other hand, the inhibitory effect induced by S. T. did not block or alter the stimulatory effect of either acetylcholine or prostigmine. Trials were made to estimate the potency of S. T. in a comparison with other skeletal muscle relaxant drugs. In this respect S. T. exhibited a more potent effect than gallamine. In contrast, other skeletal muscle relaxants (dtubocurarine, atracurium, pancuronium and succinylcholine) were highly potent. There was also a marked synergistic effect between S. T. and other neuromuscular agents.
研究了牛磺胆酸钠(S.T.)对大鼠膈神经膈肌、青蛙腹直肌以及青蛙坐骨神经腓肠肌标本收缩反应的影响。此外,还进行了S.T.与神经肌肉阻滞剂的相互作用研究。发现S.T.可使受试标本的收缩反应呈剂量依赖性降低。另一方面,S.T.诱导的抑制作用并未阻断或改变乙酰胆碱或新斯的明的刺激作用。进行了试验以评估S.T.与其他骨骼肌松弛药物相比的效力。在这方面,S.T.比加拉明表现出更强的作用。相比之下,其他骨骼肌松弛剂(筒箭毒碱、阿曲库铵、泮库溴铵和琥珀酰胆碱)效力更强。S.T.与其他神经肌肉药物之间也存在明显的协同作用。