Influence of ethacrynic acid on the anticonvulsant activity of conventional antiepileptic drugs in the mouse maximal electroshock seizure model

被引:0
|
作者
Lukawski, Krzysztof [1 ]
Swiderska, Grazyna [1 ]
Luszczki, Jarogniew J. [1 ,2 ]
Czuczwar, Stanislaw J. [1 ,2 ]
机构
[1] Inst Agr Med, Dept Physiopathol, PL-02090 Lublin, Poland
[2] Med Univ Lublin, Dept Pathophysiol, PL-20090 Lublin, Poland
关键词
ethacrynic acid; antiepileptic drugs; pharmacodynamic interaction; maximal electroshock seizure test; K-CL COTRANSPORTER; INTRINSIC OPTICAL SIGNALS; HIPPOCAMPAL SLICE; RAT; VALPROATE; EPILEPSY; FUROSEMIDE; DIURETICS; NEURONS; PHARMACOLOGY;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of this study was to determine whether ethacrynic acid (EA), a loop diuretic with anticonvulsant activity, would affect the protective action of the conventional antiepileptics (AEDs) carbamazepine (CBZ), phenytoin (PHT), valproate (VPA) and phenobarbital (PB) in the mouse maximal electroshock seizure (MES) model. The effects of acute and chronic treatment with EA on these AEDs were examined. At a single dose of 100 mg/kg ip, EA enhanced the antielectroshock activity of VPA, decreasing its ED(50) value from 225.6 to 146.6 mg/kg (p < 0.05), but enhancement was not observed following continuous administration of EA (12.5 mg/kg) for seven days. Combined treatment of EA with other AEDs had no effect on their ED50 values. The observed interaction between EA and VPA was pharmacodynamic in nature as EA did not alter free plasma (non-protein-bound) and total brain concentrations of VPA. Taking into consideration the clinical use of both drugs, this interaction between EA and VPA can be important for patients receiving these drugs.
引用
收藏
页码:808 / 813
页数:6
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