SUCCINYLCHOLINE - MECHANISM OF FASCICULATIONS AND THEIR PREVENTION BY D-TUBOCURARINE OR DIPHENYLHYDANTOIN

被引:48
作者
HARTMAN, GS
FIAMENGO, SA
RIKER, WF
机构
[1] CORNELL UNIV, MED CTR, COLL MED, DEPT ANESTHESIOL, NEW YORK, NY 10021 USA
[2] CORNELL UNIV, MED CTR, COLL MED, DEPT PHARMACOL, NEW YORK, NY 10021 USA
关键词
D O I
10.1097/00000542-198610000-00010
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Administration of d-tubocurarine (dTC) or diphenylhydantoin (DPH) was evaluated as a pretreatment to prevent succinylcholine (Sch) evoked fasciculations. Experiments were designed to determine the nature of the drug-drug interactions, sites of interaction, and site of fasciculation suppression. Sch is known to evoke repetitive discharge generation by motor nerve terminals (MNTs). Transmission of these prejunctional discharges causes fasciculations. A cat soleus neuromuscular preparation in situ, which enables recording of nerve action potentials initiated by MNTs, their transmitted muscle action potentials, and the resultant contractile responses, was used to explore Sch effects before and after iv pretreatment with dTC or DPH. dTC is known to act prejunctionally to suppress repetitive discharges initiated by facilitatory drugs and tetanic conditioning of MNTs. Accordingly, pretreatment with dTC 50 .mu.g.cntdot.kg-1 suppressed the Sch-induced MNT repetitive discharging and correspondingly suppressed generalized fasciculations without affecting twitch. This dTC dose, however, also reduced Sch blocking potency by 33%, slowed it''s rate, and shortened block duration. These latter effects represent competitive postjunctional antagonism. DPH is also known to suppress MNT repetitive discharging. Correspondingly, Sch-induced repetitive firing and ensuing fasciculations were suppressed by DPH (30 mg .cntdot. kg-1) without affecting twitch. Unlike dTC, this DPH dose increased Sch blocking potency by 50%, increased the initial rate of block, and did not alter block duration. These DPH effects were dose-dependent and within the anticonvulsant range for cats. Therefore, patients with anticonvulsant levels of DPH may not require pretreatment before Sch. It is concluded that the effectiveness of a pretreatment regimen for prevention of Sch fasciculation depends on a prejunctional suppression of repetitive firing generated by MNTs. The cat soleus preparation serves as a clinically relevant in situ method for evaluating prejunctional and postjunctional effects of drugs and should serve as a reliable test for other pretreatment candidates.
引用
收藏
页码:405 / 413
页数:9
相关论文
共 35 条
[31]   PROPERTIES OF MAXIMAL SEIZURES, AND THEIR ALTERATION BY ANTICONVULSANT DRUGS AND OTHER AGENTS [J].
TOMAN, JEP ;
SWINYARD, EA ;
GOODMAN, LS .
JOURNAL OF NEUROPHYSIOLOGY, 1946, 9 (03) :231-239
[32]  
USUBIAGA JE, 1968, J PHARMACOL EXP THER, V159, P353
[33]  
WALTS LF, 1975, MUSCLE RELAXANTS, P209
[34]   OBSERVATIONS ON PREVENTION OF MUSCLE PAINS AFTER SUXAMETHONIUM [J].
WHITE, DC .
BRITISH JOURNAL OF ANAESTHESIA, 1962, 34 (05) :332-&
[35]   DEPRESSION OF SYNAPTIC TRANSMISSION BY DIPHENYLHYDANTOIN [J].
YAARI, Y ;
PINCUS, JH ;
ARGOV, Z .
ANNALS OF NEUROLOGY, 1977, 1 (04) :334-338