Abstract | OBJECTIVE: METHODS: Wistar rats were randomly divided into 5 groups: normal control group, sham group, model group, scutellarin group and positive control group. The animal model with dementia was by bilateral ventricle injection with beta-amyloid peptide (AP) 25-35 and intraperitoneal injection with D-galactose. Learning and memory ability of rats were detected by Morris Water Maze test; Histopathology of the cerebral cortex and hippocampus were observed under light microscope; Changes of Nissl's body in the hippocampus were survey by Nissl staining; The activities of SOD and MAO were detected by xanthinoxidase method and chemical method, respectively, and neuronal apoptosis was measured using flow cytometry. RESULTS: Compared with control group and sham group, the ability of learning and memory of the rats in model group was decreased; Neuropathological changes were observed in the hippocampus; The activity of SOD was decreased while the activity of MAO increased in brain tissues; Neuronal apoptosis percentage was increased. After treated with Scutellarin, learning and memory ability of rats with dementia was improved; The pathologic changes were alleviated; The activity of SOD was up-regulation and the activity of MAO was decreased; Neuronal apoptosis percentage was declined. No significant difference between the scutellarin group and positive drug control group was found. CONCLUSION:
Scutellarin might play an therapeutic role by inhibiting oxidative stress and apoptosis in AD treatment.
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Authors | Li-li Guo, Jie Deng, Yong-lin Wang, Yong Huang, Zhi-zhong Guan |
Journal | Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials
(Zhong Yao Cai)
Vol. 34
Issue 2
Pg. 237-41
(Feb 2011)
ISSN: 1001-4454 [Print] China |
PMID | 21823483
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Amyloid beta-Peptides
- Glucuronates
- Neuroprotective Agents
- Peptide Fragments
- amyloid beta-protein (25-35)
- scutellarin
- Apigenin
- Superoxide Dismutase
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Topics |
- Alzheimer Disease
(drug therapy, pathology)
- Amyloid beta-Peptides
- Animals
- Apigenin
(pharmacology, therapeutic use)
- Apoptosis
(drug effects)
- Asarum
(chemistry)
- Cerebral Cortex
(metabolism, pathology)
- Dementia
(drug therapy, metabolism, pathology)
- Disease Models, Animal
- Female
- Glucuronates
(pharmacology, therapeutic use)
- Hippocampus
(metabolism, pathology)
- Male
- Maze Learning
(drug effects)
- Memory
(drug effects)
- Neurons
(metabolism, pathology)
- Neuroprotective Agents
(pharmacology, therapeutic use)
- Oxidative Stress
(drug effects)
- Peptide Fragments
- Random Allocation
- Rats
- Rats, Wistar
- Superoxide Dismutase
(metabolism)
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