Time-dependent decrease in the effectiveness of antiepileptic drugs during the course of self-sustaining status epilepticus

被引:178
作者
Mazarati, AM
Baldwin, RA
Sankar, R
Wasterlain, CG
机构
[1] Univ Calif Los Angeles, Sch Med, Dept Neurol, Los Angeles, CA 90024 USA
[2] Univ Calif Los Angeles, Sch Med, Dept Pediat, Los Angeles, CA 90024 USA
[3] Univ Calif Los Angeles, Sch Med, Brain Res Inst, Los Angeles, CA 90024 USA
[4] Vet Adm Med Ctr, Neurol Serv, Sepulveda, CA 91343 USA
关键词
self-sustaining status epilepticus; antiepileptic drugs; diazepam; phenytoin; refractoriness;
D O I
10.1016/S0006-8993(98)01080-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
An animal model of self-sustaining status epilepticus (SSSE) induced in rats by brief intermittent perforant path stimulation (PPS) was examined with regard to the effects of two conventional antiepileptic drugs, diazepam and phenytoin. Thirty or sixty minutes PPS induced SSSE characterized by continuous behavioral and electrographic seizures lasting for hours. Both diazepam (10 mg/kg i.v.) and phenytoin (50 mg/kg i.v,) prevented the establishment of SSSE when administered 10 min prior to PPS. The injection of diazepam to seizing animals, 10 min after the end of 30 min PPS, was significantly less effective than pretreatment in attenuating SSSE. Administration of diazepam after 60 min PPS was characterized by a further decrease of its efficacy. Phenytoin was effective in aborting SSSE when injected 10 min after 30 min PPS. However, its efficacy was vastly decreased if injected 40 min after 30 min PPS, or 10 min after 60 min PPS. It is concluded that antiepileptic drugs, while highly effective in blocking the induction of SSSE, failed to affect its maintenance. SSSE induced by PPS is an advantageous animal model of refractory status epilepticus, which may be used in preclinical studies of novel antiepileptic drugs. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:179 / 185
页数:7
相关论文
共 31 条
[1]  
[Anonymous], 1981, Epilepsia, V22, P489
[2]   BRAIN RECEPTOR-BINDING AND LIPOPHILIC CHARACTER OF BENZODIAZEPINES [J].
BOREA, PA ;
BONORA, A .
BIOCHEMICAL PHARMACOLOGY, 1983, 32 (04) :603-607
[3]  
DELORENZO RJ, 1995, J CLIN NEUROPHYSIOL, V12, P316
[4]   A prospective, population-based epidemiologic study of status epilepticus in Richmond, Virginia [J].
DeLorenzo, RJ ;
Hauser, WA ;
Towne, AR ;
Boggs, JG ;
Pellock, JM ;
Penberthy, L ;
Garnett, L ;
Fortner, CA ;
Ko, D .
NEUROLOGY, 1996, 46 (04) :1029-1035
[5]  
DODSON WE, 1993, JAMA-J AM MED ASSOC, V270, P854
[6]  
DRAKE CT, 1994, J NEUROSCI, V14, P3736
[7]   CHARACTERIZATION OF LITHIUM POTENTIATION OF PILOCARPINE-INDUCED STATUS EPILEPTICUS IN RATS [J].
JOPE, RS ;
MORRISETT, RA ;
SNEAD, OC .
EXPERIMENTAL NEUROLOGY, 1986, 91 (03) :471-480
[8]  
KANGRGA I, 1990, J NEUROSCI, V10, P2026
[9]   Experimental status epilepticus alters gamma-aminobutyric acid type A receptor function in CA1 pyramidal neurons [J].
Kapur, J ;
Coulter, DA .
ANNALS OF NEUROLOGY, 1995, 38 (06) :893-900
[10]   Rapid seizure-induced reduction of benzodiazepine and Zn2+ sensitivity of hippocampal dentate granule cell GABA(A) receptors [J].
Kapur, J ;
Macdonald, RL .
JOURNAL OF NEUROSCIENCE, 1997, 17 (19) :7532-7540