The pentylenetetrazole-kindling model of epilepsy in SAMP8 mice: behavior and metabolism

被引:29
作者
Kondziella, D
Bidar, A
Urfjell, B
Sletvold, O
Sonnewald, U [1 ]
机构
[1] Norwegian Univ Sci & Technol, Dept Clin Neurosci, N-7034 Trondheim, Norway
[2] Hannover Med Sch, Hannover, Germany
[3] Norwegian Univ Sci & Technol, Dept Imaging & Anesthesia, N-7034 Trondheim, Norway
[4] Norwegian Univ Sci & Technol, Dept Geriatr, N-7034 Trondheim, Norway
关键词
PTZ-kindling; glutamate; GABA; glutamine; SAMP8; aging;
D O I
10.1016/S0197-0186(01)00104-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This work describes a novel epilepsy model, combining pentylenetetrazole (PTZ) kindling with the senescence-accelerated mouse PS (SAMP8) a model for aging. The 2- and 8-month-old SAMP8 mice were treated with PTZ, phenobarbital plus PTZ or saline every 48 h during a period of 40 days. Both 2- and 8-month-old PTZ-kindled mice showed a behavioral pattern that was very similar to severe chronic epilepsy with secondary generalized seizures. Two out of six 8-month-old animals died in the PTZ group. Interestingly, atypical absence seizures were limited to the 8-month-old PTZ group. Furthermore, 8-month-old mice were more sensitive to the sedative effect of phenobarbital. The concentrations of several amino acids were examined by HPLC. Lower levels of amino acids were found in the 8-month-old compared to the 2-month-old control animals. No biochemical changes were observed between the groups of 2-month-old animals, while in the 8-month-old animals both treatment groups showed significantly higher concentrations of GABA, glutamine and glutathione. Thus, it could be shown that cerebral metabolism of 8-month-old SAMP8 mice was more sensitive to PTZ and phenobarbital than metabolism of 2-month-old mice. Furthermore, it is suggested that glutamate metabolism in brains of 8-month-old SAMP8 mice is altered and that excessive glutamate is transformed, in considerable amounts, into glutamate related metabolites, possibly in astrocytes. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:413 / 418
页数:6
相关论文
共 39 条
[1]   Proton magnetic resonance spectroscopy of brain biopsies from patients with intractable epilepsy [J].
Aasly, J ;
Silfvenius, H ;
Aas, TC ;
Sonnewald, U ;
Olivecrona, M ;
Juul, R ;
White, LR .
EPILEPSY RESEARCH, 1999, 35 (03) :211-217
[2]   DEFECTS OF IMMUNE CELLS IN THE SENESCENCE-ACCELERATED MOUSE - A MODEL FOR LEARNING AND MEMORY DEFICITS IN THE AGED [J].
ABE, Y ;
YUASA, M ;
KAJIWARA, Y ;
HOSONO, M .
CELLULAR IMMUNOLOGY, 1994, 157 (01) :59-69
[3]   THE INFLUENCE OF DIAZEPAM ON LEARNING-PROCESSES IMPAIRED BY PENTYLENETETRAZOL KINDLING [J].
BECKER, A ;
GRECKSCH, G ;
MATTHIES, H .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1994, 349 (05) :492-496
[4]   Magnetic resonance imaging follow-up of progressive hippocampal changes in a mouse model of mesial temporal lobe epilepsy [J].
Bouilleret, V ;
Nehlig, A ;
Marescaux, C ;
Namer, IJ .
EPILEPSIA, 2000, 41 (06) :642-650
[5]  
BRADFORD HF, 1989, EPILEPSIA, V30, P17
[6]  
De Deyn P. P., 1995, PROG NEUROBIOL, V47, P477
[7]   THE EFFECTS OF CONVULSANT AND ANTI-CONVULSANT DRUGS ON THE RELEASE OF RADIOLABELED GABA, GLUTAMATE, NORADRENALINE, SEROTONIN AND ACETYLCHOLINE FROM RAT CORTICAL SLICES [J].
DEBOER, T ;
STOOF, JC ;
VANDUIJN, H .
BRAIN RESEARCH, 1982, 253 (1-2) :153-160
[8]  
DEFEO MR, 1986, EPILEPSIA, V27, P476
[9]   CONSEQUENCES OF CHRONIC PHENOBARBITAL TREATMENT ON LOCAL CEREBRAL GLUCOSE-UTILIZATION IN THE DEVELOPING RAT [J].
DEVASCONCELOS, AP ;
BOYET, S ;
NEHLIG, A .
DEVELOPMENTAL BRAIN RESEARCH, 1990, 53 (02) :168-178
[10]   Glutathione metabolism in brain - Metabolic interaction between astrocytes and neurons in the defense against reactive oxygen species [J].
Dringen, R ;
Gutterer, JM ;
Hirrlinger, J .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2000, 267 (16) :4912-4916