Train-of-four fade during neuromuscular blockade induced by tubocurarine, succinylcholine or alpha-bungarotoxin in the rat isolated hemidiaphragm
- PMID: 2854017
- DOI: 10.1111/j.1440-1681.1988.tb01039.x
Train-of-four fade during neuromuscular blockade induced by tubocurarine, succinylcholine or alpha-bungarotoxin in the rat isolated hemidiaphragm
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.
Similar articles
-
Adenosine A(2A) receptor antagonists are broad facilitators of antinicotinic neuromuscular blockade monitored either with 2 Hz train-of-four or 50 Hz tetanic stimuli.Clin Exp Pharmacol Physiol. 2012 Oct;39(10):869-77. doi: 10.1111/j.1440-1681.2012.12004.x. Clin Exp Pharmacol Physiol. 2012. PMID: 23013133
-
In vitro time course studies on train-of-four fade induced by hexamethonium, pancuronium and decamethonium in the rat hemidiaphragm.Clin Exp Pharmacol Physiol. 1989 Dec;16(12):897-903. doi: 10.1111/j.1440-1681.1989.tb02400.x. Clin Exp Pharmacol Physiol. 1989. PMID: 2612066
-
Presynaptic muscarinic and adenosine receptors are involved in 2 Hz-induced train-of-four fade caused by antinicotinic neuromuscular relaxants in the rat.Clin Exp Pharmacol Physiol. 2011 Nov;38(11):764-70. doi: 10.1111/j.1440-1681.2011.05588.x. Clin Exp Pharmacol Physiol. 2011. PMID: 21848867
-
Neuromuscular blocking agents.Int Anesthesiol Clin. 1988 Winter;26(4):288-301. doi: 10.1097/00004311-198802640-00007. Int Anesthesiol Clin. 1988. PMID: 2848776 Review.
-
Experimental and clinical evaluation of neuromuscular blocking agents.J Pharmacol Methods. 1984 Aug;12(1):1-27. doi: 10.1016/0160-5402(84)90002-0. J Pharmacol Methods. 1984. PMID: 6100317 Review.
Cited by
-
Neuromuscular effects of candoxin, a novel toxin from the venom of the Malayan krait (Bungarus candidus).Br J Pharmacol. 2003 Jun;139(4):832-44. doi: 10.1038/sj.bjp.0705299. Br J Pharmacol. 2003. PMID: 12813007 Free PMC article.
-
Difference of train-of-four fade induced by nondepolarizing neuromuscular blocking drugs: a theoretical consideration on the underlying mechanisms.J Anesth. 1995 Dec;9(4):333-7. doi: 10.1007/BF02479947. J Anesth. 1995. PMID: 23839882
-
Block of postjunctional muscle-type acetylcholine receptors in vivo causes train-of-four fade in mice.Br J Anaesth. 2015 Jul;115(1):122-7. doi: 10.1093/bja/aev037. Epub 2015 Apr 1. Br J Anaesth. 2015. PMID: 25835024 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources