Alterations of plasma and cerebrospinal fluid glutamate levels in rats treated with the N-methyl-D-aspartate receptor antagonist, ketamine

被引:28
作者
Tomiya, Masayuki
Fukushima, Takeshi
Kawai, Junko
Aoyama, Chiaki
Mitsuhashi, Shogo
Santa, Tomofumi
Imai, Kazuhiro
Toyo'oka, Toshimasa
机构
[1] Univ Shizuoka, Sch Pharmaceut Sci, Dept Analyt Chem, Shizuoka 4228526, Japan
[2] Univ Tokyo, Grad Sch Pharmaceut Sci, Lab Bioanalyt Chem, Bunkyo Ku, Tokyo 1130033, Japan
[3] Musashino Univ, Res Inst Pharmaceut Sci, Tokyo 2028585, Japan
关键词
glutamate; ketamine; schizophrenia; HPLC; plasma; CSF;
D O I
10.1002/bmc.677
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
It has been reported that the repeated administration of a sub-anesthetic dose of an N-methyl-D-aspartate receptor antagonist, ketamine, can produce an animal model of schizophrenia. Since no information is available on the alterations of the amino acid levels in ketamine-treated rats, we investigated the amino acid composition in the plasma and cerebrospinal fluid of rats that were repeatedly administered with ketamine for 5 consecutive days (30 mg/kg/day). The plasma and cerebrospinal fluid amino acid compositions in the fifth week after cessation of repeated ketamine administration were determined by high-performance liquid chromatography with fluorescence detection using a pre-column fluorescence reagent, i.e. 4-fluoro-7nitro-2,1,3-benzoxadiazole. Among the amino acids investigated in the present study, the level of plasma glutamic acid increased significantly (p < 0.05), while that of the cerebrospinal fluid glutamic acid decreased significantly in the ketamine-treated rats as compared with these levels in control rats injected with saline (p < 0.05, n = 7). These alterations in the glutamic acid level in the plasma and cerebrospinal fluid resemble those in schizophrenic patients, suggesting that ketamine-treated rats may be a useful model for performing research on the pathophysiology of schizophrenia. Copyright (c) 2006 John Wiley & Sons, Ltd.
引用
收藏
页码:628 / 633
页数:6
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