Vigabatrin has antiepileptogenic and antidepressant effects in an animal model of epilepsy and depression comorbidity

被引:43
作者
Russo, Emilio [1 ]
Citraro, Rita [1 ]
Scicchitano, Francesca [1 ]
Urzino, Agostina [1 ]
Marra, Rosario [2 ]
Rispoli, Vincenzo [3 ]
De Sarro, Giovambattista [1 ]
机构
[1] Univ Catanzaro, Dept Expt & Clin Med, Sch Med, Chair Pharmacol, I-88100 Catanzaro, Italy
[2] Inst Neurol Sci, Natl Res Council, Catanzaro, Italy
[3] Univ Catanzaro, Dept Pharmacobiol Sci, Sch Pharm, I-88100 Catanzaro, Italy
关键词
Anticonvulsant; Absence; Epileptogenesis; SWD; Forced swimming test; GAMMA-AMINOBUTYRIC-ACID; TEMPORAL-LOBE EPILEPSY; SPIKE-WAVE DISCHARGES; LONG-TERM TREATMENT; STATUS EPILEPTICUS; PILOCARPINE MODEL; ABSENCE EPILEPSY; GABAERGIC SYSTEM; EXPRESSION; RECEPTOR;
D O I
10.1016/j.bbr.2011.07.030
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
To evaluate the effects of Vigabatrin (VGB) treatment, on both absence seizure and depressive-like behaviour development in the WAG/Rij rat model of absence seizures. Early long-term treatment with VGB could alter the development of absence pathology, by significantly reducing seizure generation and synchronization in contrast to its pro-absence effects observed after acute or subchronic administration. We have demonstrated the antidepressant effects of a sub-chronic treatment with VGB in both wistar and WAG/Rij rats. In contrast, following an early long-term treatment, VGB antidepressant effects were only observable in WAG/Rij rats. In conclusion, VGB has antiepileptogenic and antidepressant properties in the WAG/Rij rat model despite its pro-absence effects suggesting that epilepsy and depression, in this animal model, are directly related and that seizure development inhibition also reduces the development of depressive behaviour. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:373 / 376
页数:4
相关论文
共 31 条
[1]   Vigabatrin protects against hippocampal damage but is not antiepileptogenic in the lithium-pilocarpine model of temporal lobe epilepsy [J].
André, V ;
Ferrandon, A ;
Marescaux, C ;
Nehlig, A .
EPILEPSY RESEARCH, 2001, 47 (1-2) :99-117
[2]   The effects of vigabatrin on spike and wave discharges in WAG/Rij rats [J].
Bouwman, Brigitte M. ;
Suffczynski, Piotr ;
Midzyanovskaya, Inna S. ;
Maris, Eric ;
van den Broek, Philip L. C. ;
van Rijn, Clementina M. .
EPILEPSY RESEARCH, 2007, 76 (01) :34-40
[3]   Selective changes in single cell GABAA receptor subunit expression and function in temporal lobe epilepsy [J].
Brooks-Kayal, AR ;
Shumate, MD ;
Jin, H ;
Rikhter, TY ;
Coulter, DA .
NATURE MEDICINE, 1998, 4 (10) :1166-1172
[4]   Evidence for GABAergic inhibitory deficits in major depressive disorder [J].
Croarkin, Paul E. ;
Levinson, Andrea J. ;
Daskalakis, Zafiris J. .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2011, 35 (03) :818-825
[5]   The GABAB receptor as a target for antidepressant drug action [J].
Ghose, Subroto ;
Winter, Michelle K. ;
McCarson, Kenneth E. ;
Tamminga, Carol A. ;
Enna, Salvatore J. .
BRITISH JOURNAL OF PHARMACOLOGY, 2011, 162 (01) :1-17
[6]   RELATIVE ANTICONVULSANT EFFECTS OF GABAMIMETIC AND GABA MODULATORY AGENTS [J].
HOLLAND, KD ;
MCKEON, AC ;
CANNEY, DJ ;
COVEY, DF ;
FERRENDELLI, JA .
EPILEPSIA, 1992, 33 (06) :981-986
[7]   Vulnerability and plasticity of the GABA system in the pilocarpine model of spontaneous recurrent seizures [J].
Houser, CR ;
Esclapez, M .
EPILEPSY RESEARCH, 1996, 26 (01) :207-218
[8]   Seizure-induced damage to the hippocampus is prevented by modulation of the GABAergic system [J].
Jolkkonen, J ;
Halonen, T ;
Jolkkonen, E ;
Nissinen, J ;
Pitkanen, A .
NEUROREPORT, 1996, 7 (12) :2031-2035
[9]   Elevated anxiety and depressive-like behavior in a rat model of genetic generalized epilepsy suggesting common causation [J].
Jones, Nigel C. ;
Salzberg, Michael R. ;
Kumar, Gaurav ;
Couper, Abble ;
Morris, Margaret J. ;
O'Brien, Terence J. .
EXPERIMENTAL NEUROLOGY, 2008, 209 (01) :254-260
[10]   Depression and epilepsy: A bidirectional relation? [J].
Kanner, Andres M. .
EPILEPSIA, 2011, 52 :21-27