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筒箭毒碱、琥珀酰胆碱或α-银环蛇毒素诱导大鼠离体半膈肌产生神经肌肉阻滞时的四个成串刺激衰减

Train-of-four fade during neuromuscular blockade induced by tubocurarine, succinylcholine or alpha-bungarotoxin in the rat isolated hemidiaphragm.

作者信息

Cheah L S, Gwee M C

机构信息

Department of Pharmacology, Faculty of Medicine, National University of Singapore, Kent Ridge.

出版信息

Clin Exp Pharmacol Physiol. 1988 Dec;15(12):937-43. doi: 10.1111/j.1440-1681.1988.tb01039.x.

Abstract
  1. Nerve-evoked maximal twitches (T1, T2, T3, T4) of the rat isolated hemidiaphragm to train-of-four (TOF) stimulation (2 Hz X 2 s) were recorded continuously in the absence or presence of tubocurarine (1.5 mumol/l), succinylcholine (40 mumol/l) or alpha-bungarotoxin (1 mumol/l). The T1 and T4 response-time profiles for the three drugs were analysed with respect to amplitude depression and the TOF ratio (T4/T1) during the development of and recovery from neuromuscular blockade. 2. Tubocurarine produced T1 block accompanied by intense TOF fade; for the same degree of T1 block, the TOF ratio was lower during the recovery from blockade after washing out tubocurarine from the bath than during the onset of blockade. There was also a correspondingly slower recovery of the TOF ratio from 90% T1 block to control levels when compared with the time for complete T1 recovery. Fade and twitch tension depression were shown clearly to be separate responses, each with its own response-time profile. Fade is therefore not simply a consequence of postjunctional cholinoceptor blockade. 3. Succinylcholine produced T1 block with only moderate TOF fade; similar recovery rates from 90% T1 block to control levels were obtained for T1 and the TOF ratio. 4. alpha-Bungarotoxin produced irreversible and complete neuromuscular blockade during which TOF fade was virtually absent. 5. The results obtained in this study closely resemble those from other similar studies in animals and in humans and clearly demonstrate that the rat isolated hemidiaphragm is a suitable in vitro model for time course studies on TOF fade.
摘要
  1. 在不存在或存在筒箭毒碱(1.5 μmol/L)、琥珀酰胆碱(40 μmol/L)或α-银环蛇毒素(1 μmol/L)的情况下,连续记录大鼠离体半膈肌对四个成串刺激(TOF,2 Hz×2 s)的神经诱发最大抽搐(T1、T2、T3、T4)。分析了三种药物在神经肌肉阻滞形成和恢复过程中T1和T4反应时间曲线的幅度抑制和TOF比率(T4/T1)。2. 筒箭毒碱产生T1阻滞并伴有强烈的TOF衰减;对于相同程度的T1阻滞,从浴槽中洗去筒箭毒碱后,阻滞恢复期间的TOF比率低于阻滞开始时。与T1完全恢复的时间相比,从90%T1阻滞恢复到对照水平时,TOF比率的恢复也相应较慢。衰减和抽搐张力抑制显然是独立的反应,各有其自身的反应时间曲线。因此,衰减不仅仅是接头后胆碱能受体阻滞的结果。3. 琥珀酰胆碱产生T1阻滞,只有中度的TOF衰减;T1和TOF比率从90%T1阻滞恢复到对照水平的速率相似。4. α-银环蛇毒素产生不可逆的完全神经肌肉阻滞,在此期间几乎没有TOF衰减。5. 本研究获得的结果与动物和人类的其他类似研究结果非常相似,清楚地表明大鼠离体半膈肌是研究TOF衰减时间过程的合适体外模型。

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