Gastrodia elata BL Mediates the Suppression of nNOS and Microglia Activation to Protect Against Neuronal Damage in Kainic Acid-Treated Rats

Author:

Hsieh Ching-Liang12,Chen Chi-Long3,Tang Nou-Ying4,Chuang Chin-Min5,Hsieh Ching-Tou6,Chiang Su-Yin7,Lin Jaung-Geng78,Hsu Sheng-Feng48

Affiliation:

1. Department of Chinese Medicine, China Medical University Hospital, Taichung, Taiwan, ROC

2. Graduate Institute of Integration Chinese and Western Medicine, China Medical University, Taichung, Taiwan, ROC

3. Department of Pathology, Taipei Medical University, Taipei, Taiwan, ROC

4. School of Chinese Medicine, China Medical University, Taichung, Taiwan, ROC

5. Emergency Department, China Medical University Hospital, Taichung, Taiwan, ROC

6. Department of Internal Medicine, Jen-Ai Hospital, Taichung, Taiwan, ROC

7. Graduate Institute of Chinese Medical Science, College of Chinese Medicine, China Medical University, Taichung, Taiwan, ROC

8. Acupuncture Research Center, China Medical University, Taichung, Taiwan, ROC

Abstract

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 μg/2 μl) 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.

Publisher

World Scientific Pub Co Pte Lt

Subject

Complementary and alternative medicine,General Medicine

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