Gastrodia elata BL mediates the suppression of nNOS and microglia activation to protect against neuronal damage in kainic acid-treated rats

被引:32
作者
Hsieh, CL
Chen, CL
Tang, NY
Chuang, CM
Hsieh, CT
Chiang, SY
Lin, JG
Hsu, SF
机构
[1] China Med Univ Hosp, Dept Chinese Med, Taichung, Taiwan
[2] China Med Univ Hosp, Dept Emergency, Taichung, Taiwan
[3] China Med Univ, Grad Inst Integrat Chinese & Western Med, Taichung, Taiwan
[4] China Med Univ, Coll Chinese Med, Sch Chinese Med, Taichung 404, Taiwan
[5] China Med Univ, Coll Chinese Med, Sch Chinese Med, Taichung 404, Taiwan
[6] China Med Univ, Grad Inst Chinese Med Sci, Coll Chinese Med, Taichung, Taiwan
[7] China Med Univ, Acupuncture Res Ctr, Taichung, Taiwan
[8] Taipei Med Univ, Dept Pathol, Taipei, Taiwan
[9] Jen Ai Hosp, Dept Internal Med, Taichung, Taiwan
来源
AMERICAN JOURNAL OF CHINESE MEDICINE | 2005年 / 33卷 / 04期
关键词
Gastrodia elata; kainic acid; microglia; apoptosis; nitric oxide synthase (NOS);
D O I
10.1142/S0192415X0500320X
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Our previous studies showed that Gastrodia elata (GE), an herb used in traditional Chinese medicine, has both anti-convulsive and free radical-scavenging activities in kainic acid (KA)-treated rats. The aim of the present study was to further investigate possible physiological mechanisms of GE against activities of neuronal nitric oxide synthase (nNOS) and microglia in KA-treated rats; 0.5 g/kg and 1.0 g/kg of GE extract were administered orally, whereas 20 mg/kg of N-nitro-L-arginine methyl ester (L-NAME) was administered intraperitoneally (ip), both at 30 minutes prior to KA (2 mu g/2 mu l) being injected into the right hippocampus region of rats. ED1-staining, apoptotic, inducible nitric oxide synthase (iNOS), and nNOS-staining cells were observed in the hippocampus region. The results indicated that 1.0 g/kg of GE and 20 mg/kg of L-NAME reduced the counts of ED1-stained cells, and 0.5 g/kg and 1.0 g/kg of GE, and 20 mg/kg of L-NAME reduced the numbers of apoptotic cells and nNOS-staining cells. In addition, 20 mg/kg of L-NAME also reduced the numbers of iNOS-staining cells, but 0.5 g/kg and 1.0 g/kg of GE did not. This study demonstrated that GE was able to reduce nNOS, microglia activation and apoptosis, suggesting that GE has a protective effect against neuronal damage in KA-treated rats.
引用
收藏
页码:599 / 611
页数:13
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