Inhibition of the enzymic degradation of suxamethonium and mivacurium increases the onset time of submaximal neuromuscular block

被引:19
作者
Beaufort, TM [1 ]
Nigrovic, V [1 ]
Proost, JH [1 ]
Houwertjes, MC [1 ]
Wierda, JMKH [1 ]
机构
[1] Univ Groningen, Res Grp Expt Anesthesiol & Clin Pharmacol, Groningen, Netherlands
关键词
neuromuscular blocking agents; onset of action; plasma clearance; time course of action;
D O I
10.1097/00000542-199809000-00022
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background: The factors that influence the onset time of submaximal (<100%) neuromuscular block are not fully known. The authors hypothesized that differences in the rate of decrease in the plasma concentration result in differences in the rate of equilibration between plasma and biophase and thus in different onset times. If this hypothesis is valid inhibition of the enzymic degradation of muscle relaxants should increase the onset time of neuromuscular block Methods: Twenty pigs received either suxamethonium or mivacurium Dose finding (70% block) was done for each pig. The enzymic degradation of the muscle relaxant was randomly inhibited by selective inhibition of plasma cholinesterase activity by tetraisopropyl pyrophosphoramide (10 pigs) or was not inhibited (10 pigs). Plasma cholinesterase activities and the mechanomyographic muscle response after peroneal nerve stimulation (0.1 Hz) were measured. Results: Inhibition of plasma cholinesterase activity (by 93% and 89%, respectively) increased the onset time of suxamethonium from a median of 40 s (range, 20-45 s) to 131 s (range, 114-166 s; P = 0.009) and of mivacurium from a median of 52 s (range, 40-59 s) to 105 s (range, 90-125 s; P = 0.009). Inhibition of degradation decreased the effective dose of suxamethonium that resulted in 70% depression of the initial twitch height from 900 mu g/kg (range, 400-1,000 mu g/kg) to 150 mu g/kg (range, 135-150 mu g/kg) and of mivacurium from 100 mu g/kg (range, 80-150 mu g/kg) to 35 mu g/kg (range, 20-50 mu g/kg). Conclusions: Inhibition of the enzymic degradation of suxamethonium and mivacurium increases the onset time of submaximal neuromuscular block Therefore, pharmacokinetics influence the onset time of submaximal neuromuscular block. These results imply that to obtain an ultrashort onset time, muscle relaxants should be developed that not only have a low affinity for the receptor but also rapidly disappear from plasma.
引用
收藏
页码:707 / 714
页数:8
相关论文
共 39 条
[1]   RAPID ONSET OF SUXAMETHONIUM BLOCK [J].
BARAKA, A .
BRITISH JOURNAL OF ANAESTHESIA, 1991, 66 (06) :733-733
[2]   STRUCTURE - ACTION RELATIONSHIPS AMONG SOME DESACETOXY ANALOGS OF PANCURONIUM AND VECURONIUM IN THE ANESTHETIZED CAT [J].
BOWMAN, WC ;
RODGER, IW ;
HOUSTON, J ;
MARSHALL, RJ ;
MCINDEWAR, I .
ANESTHESIOLOGY, 1988, 69 (01) :57-62
[3]   REPEATED ADMINISTRATION OF SUXAMETHONIUM IN A PATIENT WITH ATYPICAL PLASMA CHOLINESTERASE [J].
CASS, NM ;
DOOLAN, LA ;
GUTTERIDGE, GA .
ANAESTHESIA AND INTENSIVE CARE, 1982, 10 (01) :25-28
[5]   PHARMACOKINETICS OF MIVACURIUM IN NORMAL-PATIENTS AND IN THOSE WITH HEPATIC OR RENAL-FAILURE [J].
COOK, DR ;
FREEMAN, JA ;
LAI, AA ;
KANG, Y ;
STILLER, RL ;
AGGARWAL, S ;
HARRELSON, JC ;
WELCH, RM ;
SAMARA, B .
BRITISH JOURNAL OF ANAESTHESIA, 1992, 69 (06) :580-585
[6]  
DONATI F, 1988, Canadian Journal of Anaesthesia, V35, pS52
[7]  
DONATI F, 1993, ANAESTHETIC PHARM RE, V1, P34
[8]  
FAUVEL NJ, 1993, ANAESTH PHARM REV, V1, P44
[9]  
GLAVINOVIC MI, 1993, J PHARMACOL EXP THER, V265, P1181
[10]   EFFECT OF BLOOD-FLOW UPON ACTIVITY OF GALLAMINE TRIETHIODIDE [J].
GOAT, VA ;
YEUNG, ML ;
BLAKENEY, C ;
FELDMAN, SA .
BRITISH JOURNAL OF ANAESTHESIA, 1976, 48 (02) :69-73