Mexiletine and its Interactions with Classical Antiepileptic Drugs: An Isobolographic Analysis

被引:9
作者
Borowicz-Reutt, Kinga K. [1 ]
Banach, Monika [1 ]
Piskorska, Barbara [1 ]
机构
[1] Med Univ Lublin, Dept Pathophysiol, Independent Unit Expt Neuropathophysiol, Lublin, Poland
关键词
Mexiletine; Antiepileptic drugs; Maximal electroshock; Drug interactions; Isobolographic analysis; ANTICONVULSANT ACTIVITY; GABAPENTIN; SEIZURES; EPILEPSY; MODEL; MICE;
D O I
10.1007/s11064-015-1812-x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Using the mouse maximal electroshock test, the reference model of tonic-clonic seizures, the aim of the present study was to determine the type of interaction between mexiletine (a class IB antiarrhythmic drug) and classical antiepileptics: valproate, carbamazepine, phenytoin, and phenobarbital. Isobolographic analysis of obtained data indicated antagonistic interactions between mexiletine and valproate (for fixed ratio combinations of 1:1 and 3:1). Additivity was observed between mexiletine and valproate applied in proportion of 1:3 as well as between mexiletine and remaining antiepileptics for the fixed ratios of 1:3, 1:1, and 3:1. Neither motor performance nor long-term memory were impaired by mexiletine or antiepileptic drugs regardless of whether they were administered singly or in combination. Mexiletine did not significantly affected brain concentrations of carbamazepine, phenobarbital or phenytoin. In contrast, the antiarrhythmic drug decreased by 23 % the brain level of valproate. This could be, at least partially, the reason of antagonistic interaction between the two drugs. In conclusion, the observed additivity suggests that mexiletine can be safely applied in epileptic patients treated with carbamazepine, phenytoin or phenobarbital. Because of undesirable pharmacodynamics and pharmacokinetic interactions with valproate, mexiletine should not be used in such combinations.
引用
收藏
页码:1185 / 1191
页数:7
相关论文
共 22 条
[1]  
ALEXANDER GJ, 1986, NEUROBEH TOXICOL TER, V8, P231
[2]  
BOISSIER J.-R, 1960, MED EXPTL, V3, P81
[3]   Acute and chronic treatment with mianserin differentially affects the anticonvulsant activity of conventional antiepileptic drugs in the mouse maximal electroshock model [J].
Borowicz, Kinga K. ;
Banach, Monika ;
Zarczuk, Radoslaw ;
Lukasik, Dariusz ;
Luszczki, Jarogniew J. ;
Czuczwar, Stanislaw J. .
PSYCHOPHARMACOLOGY, 2007, 195 (02) :167-174
[4]   Effect of gabapentin on the anticonvulsant activity of antiepileptic drugs against electroconvulsions in mice: An isobolographic analysis [J].
Borowicz, KK ;
Swiader, M ;
Luszczki, J ;
Czuczwar, SJ .
EPILEPSIA, 2002, 43 (09) :956-963
[5]   THE MAXIMAL ELECTROSHOCK SEIZURE (MES) MODEL IN THE PRECLINICAL ASSESSMENT OF POTENTIAL NEW ANTIEPILEPTIC DRUGS [J].
Castel-Branco, M. M. ;
Alves, G. L. ;
Figueiredo, I. V. ;
Falcao, A. C. ;
Caramona, M. M. .
METHODS AND FINDINGS IN EXPERIMENTAL AND CLINICAL PHARMACOLOGY, 2009, 31 (02) :101-106
[6]   The new generation of GABA enhancers - Potential in the treatment of epilepsy [J].
Czuczwar, SJ ;
Patsalos, PN .
CNS DRUGS, 2001, 15 (05) :339-350
[7]   Current limitations of antiepileptic drug therapy: a conference review [J].
Deckers, CLP ;
Genton, P ;
Sills, GJ ;
Schmidt, D .
EPILEPSY RESEARCH, 2003, 53 (1-2) :1-17
[8]   Selection of antiepileptic drug polytherapy based on mechanisms of action: The evidence reviewed [J].
Deckers, CLP ;
Czuczwar, SJ ;
Hekster, YA ;
Keyser, A ;
Kubova, H ;
Meinardi, H ;
Patsalos, PN ;
Renier, WO ;
Van Rijn, CM .
EPILEPSIA, 2000, 41 (11) :1364-1374
[9]  
Enoki Hideo, 2000, No To Hattatsu, V32, P29
[10]  
LITCHFIELD JT, 1949, J PHARMACOL EXP THER, V96, P99