Specific group II metabotropic glutamate receptor activation inhibits the development of kindled epilepsy in rats

被引:47
作者
Attwell, PJE
Koumentaki, A
Croucher, MJ
Bradford, HF
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Biochem, London SW7 2AY, England
[2] Charing Cross Hosp, Imperial Coll, Sch Med,Div Neurosci & Psychol Med, Dept Neurodegenerat Disorders, London W6 8RF, England
基金
英国惠康基金;
关键词
anticonvulsant; epileptogenesis; 2R; 4R-APDC; group II metabotropic glutamate receptor; glutamate; kindling;
D O I
10.1016/S0006-8993(97)01500-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The effects of intracerebral administration of the group II metabotropic glutamate receptor agonist, 2R,4R-APDC, were tested on both the development of amygdaloid kindling and on fully developed stage 5 amygdala kindled seizures. The development of amygdaloid kindling was significantly retarded in 2R,4R-APDC (10 nmol in 0.5 mu l) treated animals compared to control animals over a period of 8 days. At a low dose, 2R,4R-APDC (0.1 nmol) caused a 42.5 +/- 26.6% increase of the generalised seizure threshold in fully kindled animals. As higher doses were administered, however, the changes in generalised seizure threshold were less marked, and even a small decrease in the threshold was seen (-19.6 +/- 5.36% at 10 nmol). The agonist 2R,4R-APDC inhibited depolarization-induced release of [H-3]D-aspartate from cortical synaptosomes with an IC50 value of 0.29 mu M. This effect was maximal at 1 mu M, and decreased with dose thereafter. These findings suggest that the selective activation of the group II metabotropic glutamate receptors by agonists such as 2R,4R-APDC may be of therapeutic potential in the treatment of seizure disorders. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:286 / 291
页数:6
相关论文
共 39 条
[1]   Anti-epileptogenic and anticonvulsant activity of L-2-amino-4-phosphonobutyrate, a presynaptic glutamate receptor agonist [J].
AbdulGhani, AS ;
Attwell, PJE ;
Kent, NS ;
Bradford, HF ;
Croucher, MJ ;
Jane, DE .
BRAIN RESEARCH, 1997, 755 (02) :202-212
[2]   BLOCKADE OF BOTH EPILEPTOGENESIS AND GLUTAMATE RELEASE BY (1S,3S)-ACPD, A PRESYNAPTIC GLUTAMATE-RECEPTOR AGONIST [J].
ATTWELL, PJE ;
KAURA, S ;
SIGALA, G ;
BRADFORD, HF ;
CROUCHER, MJ ;
JANE, DE ;
WATKINS, JC .
BRAIN RESEARCH, 1995, 698 (1-2) :155-162
[3]   Glutamate, GABA and epilepsy [J].
Bradford, HF .
PROGRESS IN NEUROBIOLOGY, 1995, 47 (06) :477-511
[4]  
BRADFORD HF, 1996, INT MED J, V3, P183
[5]   POTENT ORAL ANTICONVULSANT ACTION OF CPP AND CPPENE IN DBA/2 MICE [J].
CHAPMAN, AG ;
GRAHAM, J ;
MELDRUM, BS .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1990, 178 (01) :97-99
[6]   IS GLUTAMATE A TRIGGER FACTOR IN EPILEPTIC HYPERACTIVITY [J].
COUTINHONETTO, J ;
ABDULGHANI, AS ;
COLLINS, JF ;
BRADFORD, HF .
EPILEPSIA, 1981, 22 (03) :289-296
[7]   KINDLING OF FULL LIMBIC SEIZURES BY REPEATED MICROINJECTIONS OF EXCITATORY AMINO-ACIDS INTO THE RAT AMYGDALA [J].
CROUCHER, MJ ;
BRADFORD, HF .
BRAIN RESEARCH, 1989, 501 (01) :58-65
[8]   COMPETITIVE NMDA RECEPTOR ANTAGONISTS RAISE ELECTRICALLY KINDLED GENERALIZED SEIZURE THRESHOLDS [J].
CROUCHER, MJ ;
COTTERELL, KL ;
BRADFORD, HF .
NEUROCHEMICAL RESEARCH, 1992, 17 (05) :409-413
[9]   NMDA RECEPTOR BLOCKADE INHIBITS GLUTAMATE-INDUCED KINDLING OF THE RAT AMYGDALA [J].
CROUCHER, MJ ;
BRADFORD, HF .
BRAIN RESEARCH, 1990, 506 (02) :349-352
[10]   ANTICONVULSANT ACTION OF EXCITATORY AMINO-ACID ANTAGONISTS [J].
CROUCHER, MJ ;
COLLINS, JF ;
MELDRUM, BS .
SCIENCE, 1982, 216 (4548) :899-901