Involvement of nitric oxide and nitric oxide synthase activity in anticonvulsive action

被引:25
作者
Jayakumar, AR
Sujatha, R
Paul, V
Puviarasan, K
Jayakumar, R [1 ]
机构
[1] Cent Leather Res Inst, Bioorgan Lab, Adyar 600020, Chennai, India
[2] ALM Postgrad Inst Basic Med Sci, Dept Pharmacol, Taramani, Chennai, India
[3] Univ Madras, Dept Crystallog & Biophys, Madras, Tamil Nadu, India
关键词
nitric oxide; nitric oxide synthase; anticonvulsant; convulsion latency; convulsion frequency; L-arginine; diazepam; picrotoxin;
D O I
10.1016/S0361-9230(99)00011-8
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
The anticonvulsant drug Diazepam (DIA-2 mg/kg b. wt), the nitric oxide (NO) donor L-Arginine (L-Arg-2000 mg/kg b. wt) and the putative nitric oxide synthase (NOS) inhibitor NG-Nitro-L-Arginine methyl ester (L-NAME-50 mg/kg b. wt) were used to determine the role of endogenous NO on convulsions induced by picrotoxin (PCT-5 mg/kg b. wt) in rats. Rats given a convulsant dose of PCT (5 mg/kg b. wt) had convulsion and it suppresses the NOS activity and NO concentration in brain regions. The anticonvulsant L-Arg alone significantly increases the NO concentration and NOS activity in brain regions, but not diazepam. Whereas DIA, along with L-Arg, enhances the NO and NOS activity when compared to L-Arg alone. The combination of both OIA and L-Arg completely suppressed the convulsions. L-NAME alone had no effect to produce convulsions but it completely decreased NO concentration and NOS activity and potentiated the PCT convulsions. This was reverted by pre- and post treatment of DIA plus L-Arg indicating, the increased NO concentration and NOS activity in brain regions suppresses convulsions. (C) 1999 Elsevier Science Inc.
引用
收藏
页码:387 / 394
页数:8
相关论文
共 37 条
[1]
N-G-Nitro-L-[H-3]arginine binding properties of neuronal nitric oxide synthase in rat brain [J].
Arima, T ;
Kitamura, Y ;
Nishiya, T ;
Kiriyama, Y ;
Taniguchi, T ;
Nomura, Y .
NEUROCHEMISTRY INTERNATIONAL, 1997, 30 (03) :239-245
[2]
TACRINE-INDUCED SEIZURES AND BRAIN-DAMAGE IN LICL-TREATED RATS CAN BE PREVENTED BY N-OMEGA-NITRO-L-ARGININE METHYL-ESTER [J].
BAGETTA, G ;
IANNONE, M ;
SCORSA, AM ;
NISTICO, G .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1992, 213 (02) :301-304
[3]
The effect of chronic cyclodiene insecticide treatment on some pharmacological actions of diazepam in rats [J].
Balasubramaniam, E ;
Paul, V ;
Jayakumar, AR ;
Kazi, M .
ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY, 1996, 1 (02) :141-146
[4]
NITRIC-OXIDE - AN ENDOGENOUS ANTICONVULSANT SUBSTANCE [J].
BUISSON, A ;
LAKHMECHE, N ;
VERRECCHIA, C ;
PLOTKINE, M ;
BOULU, RG .
NEUROREPORT, 1993, 4 (04) :444-446
[5]
Cyclic AMP potentiation of cytokine-induced nitric oxide synthase activity in a murine astrocyte cell line [J].
Burgher, KL ;
Heroux, JA ;
Ringheim, GE .
NEUROCHEMISTRY INTERNATIONAL, 1997, 30 (4-5) :483-489
[6]
Expression and plasticity of NO synthase in the neuroendocrine system [J].
Ceccatelli, S .
BRAIN RESEARCH BULLETIN, 1997, 44 (04) :533-538
[7]
Nitric oxide involvement in regulating the dopamine transport in the striatal region of rat brain [J].
ChaparroHuerta, V ;
BeasZarate, C ;
Guerrero, MU ;
FeriaVelasco, A .
NEUROCHEMISTRY INTERNATIONAL, 1997, 31 (04) :607-616
[8]
Chen CH, 1997, AVIAT SPACE ENVIR MD, V68, P296
[9]
7-nitroindazole prevents dopamine depletion caused by low concentrations of MPP+ in rat striatal slices [J].
Cutillas, B ;
Espejo, M ;
Ambrosio, S .
NEUROCHEMISTRY INTERNATIONAL, 1998, 33 (01) :35-40
[10]
L-ARGININE POTENTIATES EXCITATORY AMINO ACID-INDUCED SEIZURES ELICITED IN THE DEEP PREPIRIFORM CORTEX [J].
DESARRO, G ;
DIPAOLA, ED ;
DESARRO, A ;
VIDAL, MJ .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1993, 230 (02) :151-158