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首页> 外文期刊>Autonomic & autacoid pharmacology >Pharmacodynamic interaction between pantoprazole and vecuronium at neuromuscular junction.
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Pharmacodynamic interaction between pantoprazole and vecuronium at neuromuscular junction.

机译:神经肌肉连接处pantraprazole和Vecuronium之间的药效学相互作用。

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1 The effect of pantoprazole on vecuronium-induced neuromuscular blockade in in vivo has not been clearly defined. In this study, we demonstrate that chronic administration, but not acute administration, of pantoprazole alters the pattern of vecuronium-induced neuromuscular blockade. 2 This study was designed to evaluate the effect of acute and chronic administration of pantoprazole on vecuronium-induced neuromuscular blockade using the rat in vivo sciatic nerve-stimulated gastrocnemius preparation. 3 Vecuronium was administered as a slow intravenous infusion (29.41 mug kg(-1) min(-1)) until the gastrocnemius twitch response to sciatic nerve stimulation was completely abolished. The effect of acute (single dose, i.v.) and chronic administration (per oral for 21 days) of pantoprazole (3.64 mg kg(-1)) on vecuronium-induced blockade was assessed by comparing ED50 values, time required for 50% block, ED95 values, block duration and percentage of recovery with respect to control. 4 Acute administration of pantoprazole had no significant effect on any parameter of vecuronium-induced neuromuscular blockade. Chronic administration of pantoprazole significantly reduced vecuronium ED50 value, time for 50% block, ED95 value and percentage recovery from blockade compared with the control group (P<0.05). Reduction in the duration of vecuronium-induced blockade was not significantly affected by chronic treatment with pantoprazole compared with control. 5 On chronic administration, pantoprazole may produce earlier block, quick relaxation and reduces the recovery of vecuronium without affecting its duration of action.
机译:1吡唑唑对体内载体诱导的神经肌肉阻滞的影响尚未明确定义。在这项研究中,我们证明了pantoprazole的慢性给药但不进行急性给药,会改变敌对诱导的神经肌肉阻滞的模式。 2这项研究旨在评估使用大鼠在体内坐骨神经刺激的胃神经抑制剂中,急性和长期给药pantoprazole对耐龙诱导的神经肌肉阻滞的影响。 3拟耐酸被作为缓慢的静脉输注(29.41杯kg(-1)min(-1)),直到完全废除了对坐骨神经刺激的胃nius肌抽搐反应。通过比较ED50值,50%块所需的时间,评估了急性(单剂量,i.v. ED95值,块持续时间和恢复百分比相对于对照。 4急性施用pantoprazole对壁球诱导的神经肌肉阻滞的任何参数没有显着影响。与对照组相比,长期给药pantoprazole可显着降低vecuronium ED50值,50%块的时间,ED95值和从封锁的百分比回收率(p <0.05)。与对照相比,用吡丙唑唑慢性治疗的持续时间降低了壁球诱导的封锁的持续时间没有显着影响。 5在慢性给药上,pantraprazole可能会产生较早的障碍,快速放松并减少壁的恢复,而不会影响其作用持续时间。

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