Gastrodin decreases immunoreactivities of γ-aminobutyric acid shunt enzymes in the hippocampus of seizure-sensitive gerbils

被引:80
作者
An, SJ
Park, SK
Hwang, IK
Choi, SY
Kim, SK
Kwon, OS
Jung, SJ
Baek, NI
Lee, HY
Won, MH
Kang, TC [1 ]
机构
[1] Hallym Univ, Coll Med, Dept Anat, Chunchon 200702, Kangwon Do, South Korea
[2] Hallym Univ, Coll Life Sci, Dept Genet Engn, Chunchon, South Korea
[3] Kyungpook Natl Univ, Coll Nat Sci, Dept Biochem, Taegu 702701, South Korea
[4] Kyung Hee Univ, Dept Life Sci, Suwon, South Korea
[5] Kyung Hee Univ, Plant Metab Res Ctr, Suwon, South Korea
[6] Kangwon Natl Univ, Div Food & Biotechnol, Chunchon, South Korea
关键词
gastrodin; gerbil; epilepsy; GABA shunt; GAD; GABA transporter; hippocampus;
D O I
10.1002/jnr.10502
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Gastrodin is one of the natural compound isolated from Gastrodia elata and has known anticonvulsant effects, although the exact pharmacological principles of this natural compound and its effects on other aspects of gamma-aminobutyric acid (GABA) metabolism in vivo have not been explored. Therefore, in the present study, the effects of gastrodin on GABA metabolism in the gerbil hippocampus were examined, in an effort to identify the antiepileptic characteristics of this substance. Gastrodin reduced the seizure score in the treated group, although the immunoreactivities of GABA synthetic enzymes and GABA transporters were unaltered in gastrodin-treated animals. Interestingly, in the gastrodin-treated group, GABA transaminase (GABA-T) immunoreactivity in the hippocampus, particularly in neurons, was significantly decreased. In the gastrodin-treated group, both succinic semialdehyde dehydrogenase (SSADH) and succinic semialdehyde reductase (SSAR) immunoreactivities in the hippocampus was also decreased significantly, which stood in contrast to the nontreated group, in which strong SSADH and SSAR immunoreactivities were detected. From the neuroanatomical viewpoint, these findings suggest that gastrodin may cause the elevation of GABA concentration by inhibiting the GABA shunt. (C) 2002 Wiley-Liss, Inc.
引用
收藏
页码:534 / 543
页数:10
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