RESEARCH PAPER
Isobolographic interaction between AO-294, an enantiomer of losigamone, and phenobarbital in the mouse model of maximal electroshock
 
More details
Hide details
1
Experimental Neuropathophysiology Unit, Department of Pathophysiology, Medical University, Lublin, Poland
 
 
Corresponding author
Kinga Borowicz   

Department of Pathophysiology, Medical University, Jaczewskiego 8, 20-090 Lublin, Poland.
 
 
J Pre Clin Clin Res. 2007;1(1):41-42
 
KEYWORDS
ABSTRACT
The objective of the present study was to determine the exact type of interaction between AO-294, the less active enantiomer of a novel antiepileptic drug losigamone and phenobarbital in the model of maximal electroshock-induced convulsions in mice. Isobolographic analysis of obtained data show that the 2 drugs interact additively when administered in proportions of 1:3 and 1:1. Antagonism was found at the dose ratio of 3:1. This may suggest that AO-294 is not a good candidate for 2-drug therapy with phenobarbital, especially when administered at relatively high doses.
REFERENCES (9)
1.
Borowicz KK, Małek R, Kimber-Trojnar Z, Sobieszek G: Isobolographic analysis of the interactions of losigamone, remacemide, zonisamide with conventional antiepileptic drugs in the maximal electroshock test in mice – preliminary report. Neurol Neurochir Pol 2003, 3, 35-36.
 
2.
Gąsior M, Ungard JT, Witkin JM: Preclinical evaluation of newly approved and potential antiepileptic drugs against cocaine-induced seizures. J Pharmacol Exp Ther 1999, 290, 1148-1156.
 
3.
Bialer M, Johannessen SI, Kupferberg HJ, Levy RH, Loiseau P, Perucca E: Progress report on new antiepileptic drugs: a summary of the 4th Eilat conference (EILAT IV). Epilepsy Res 1999, 34, 1-41.
 
4.
Jones FA, Davies JA: The anticonvulsant effects of the enantiomers of losigamone. Br J Pharmacol 1999, 128, 1223-1228.
 
5.
Dimpfel W, Chatterje SS, Noldner M, Ticku MK: Effects of the anticonvulsant losigamone and its isomers on GABA-receptor system. Epilepsia 1995, 36, 983-989.
 
6.
Litchfield JT, Wilcoxon F: A simplified method of evaluating dose-effect experiments. J Pharmacol Exp Ther 1949, 96, 99–113.
 
7.
Loewe S: The problem of synergism and antagonism of combined drugs. Arzneimittelforschung 1953, 3, 285-290.
 
8.
Łuszczki JJ, Czuczwar SJ: Isobolographic characterization of interactions among selected newer antiepileptic drugs in the mouse pentylenetetrazole-induced seizure model. Naunyn Schmiedeberg’s Arch Pharmacol 2005, 372, 41-54.
 
9.
Tallarida RJ, Stone DJ, Raffa RB: Efficient designs for studying synergistic drug combinations. Life Sci 1997, 61, 417–425.
 
eISSN:1898-7516
ISSN:1898-2395
Journals System - logo
Scroll to top