Abstract | OBJECTIVE: METHODS: One hundred male Wistar rats (180-220 g) were divided into ten groups randomly, they were sham operated group (SOG, n = 10), three model group(MG-ld, 3d, 7d, n = 10), as well as three low and high dose astragalan treatment groups (L/H-AGTG-1d, 3d, 7d, n = 10), respectively. And then, middle cerebral artery of MG and AGTG were intercepted by operation inducing brain injured. Their cerebral blood vessel were reperfused on 1, 2, 3 d, respectively, after the L/H-AGTG were treated with the AG (5 mg/kg and 15 mg/kg, ip). After neurologic impairment(NIP) was scored, animals were decapitated to take out hippocampus for counting apoptosis , determining the expression of the NCAM and c-fos by immunohistochemistry method and RT-PCR semiquantitative analysis, respectively. RESULTS: The NIP scores and apoptotic cell of the L-AGTG and H-AGTG were significantly lower than MG (P < 0.05 or P < 0.01). The expression of NCAM and c-fos were significantly higher than the MG (P < 0.05 or P < 0.01). CONCLUSION: Astragalan could improve significantly neural function of ischemia brain injury in rats,the mechanism concerned probably with blocking or reversing apoptosis of hippocampus by promoting the expression of the NCAM and c-fos of hippocampus CA1 region.
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Authors | Ling Yan, Qing-Hua Zhou |
Journal | Zhongguo ying yong sheng li xue za zhi = Zhongguo yingyong shenglixue zazhi = Chinese journal of applied physiology
(Zhongguo Ying Yong Sheng Li Xue Za Zhi)
Vol. 28
Issue 4
Pg. 373-7
(Jul 2012)
ISSN: 1000-6834 [Print] China |
PMID | 23156741
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Kaempferols
- Neural Cell Adhesion Molecules
- Neuroprotective Agents
- Polysaccharides
- astragalin
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Topics |
- Animals
- Apoptosis
(drug effects)
- Astragalus propinquus
(chemistry)
- Brain Ischemia
(metabolism, pathology)
- CA1 Region, Hippocampal
(cytology)
- Kaempferols
(pharmacology)
- Male
- Neural Cell Adhesion Molecules
(metabolism)
- Neurons
(drug effects)
- Neuroprotective Agents
(pharmacology)
- Polysaccharides
(pharmacology)
- Rats
- Rats, Wistar
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