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Research ArticleORIGINAL ARTICLES
Open Access

Allicin can reduce neuronal death and ameliorate the spatial memory impairment in Alzheimers disease models

Xian-Hui Li, Chun-Yan Li, Zhi-Gang Xiang, Fei Zhong, Zheng-Ying Chen and Jiang-Ming Lu
Neurosciences Journal October 2010, 15 (4) 237-243;
Xian-Hui Li
Institute of Medicine of Jishou University, Jishou 416000, Hunan Province, China. Tel. +86 (1303) 7430956. Fax. +86 (743) 8565171. E-mail: [email protected]
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Chun-Yan Li
Institute of Medicine of Jishou University, Jishou 416000, Hunan Province, China. Tel. +86 (1303) 7430956. Fax. +86 (743) 8565171. E-mail: [email protected]
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Zhi-Gang Xiang
Institute of Medicine of Jishou University, Jishou 416000, Hunan Province, China. Tel. +86 (1303) 7430956. Fax. +86 (743) 8565171. E-mail: [email protected]
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Fei Zhong
Institute of Medicine of Jishou University, Jishou 416000, Hunan Province, China. Tel. +86 (1303) 7430956. Fax. +86 (743) 8565171. E-mail: [email protected]
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Zheng-Ying Chen
Institute of Medicine of Jishou University, Jishou 416000, Hunan Province, China. Tel. +86 (1303) 7430956. Fax. +86 (743) 8565171. E-mail: [email protected]
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Jiang-Ming Lu
Institute of Medicine of Jishou University, Jishou 416000, Hunan Province, China. Tel. +86 (1303) 7430956. Fax. +86 (743) 8565171. E-mail: [email protected]
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Abstract

OBJECTIVE: To investigate the mechanisms and protective effects of allicin on learning and memory in a mouse model of Alzheimer’s disease (AD).

METHODS: This study took place in the Institute of Medicine of Jishou University, Jishou, China, between January and September 2009. Allicin was given as preventive administration after AD was induced by amyloid beta (AÕ[1-42]), and the protective effects of Allicin against learning and memory impairment were investigated. Sixty mice were randomly divided into 3 groups including the sham-operated+phosphate buffer solution (PBS) group, the AÕ(1-42)+PBS group, and the AÕ(1-42)+allicin group. The AÕ(1-42) (1 µL = 4µg) was injected into the bilateral hippocampi. Sham-operated mice were infused with PBS. Allicin or PBS was then injected intraperitoneally for 14 days. The animals were trained, and learning and memory abilities tested using the Morris Water-Maze. The changes of AÕ(1-42) and P38 mitogen-activated protein kinase (p38MAPK) were recorded to explore the mechanism of allicin’s protective effects on learning and memory deficits.

RESULTS: The AÕ(1-42)-infused allicin-treated group showed significantly shorter latency times than the PBS treated AÕ(1-42)-infused group from the second day of learning sessions (p=0.031), accompanied with significant reduction of malondialdehyde (MDA) (p=0.035) and an increase of superoxide dismutase (SOD) activity (p=0.041). Allicin also decreased AÕ and p38MAPK expressions in the cerebral cortex of AD mice model (p=0.031).

CONCLUSION: Preventive administration of allicin prevented learning and memory impairment, the mechanism may be due to an increase in the activity of SOD, a reduction in the levels of MDA and the expressions of AÕ and p38MAPK in the brain.

  • Copyright: © Neurosciences

Neurosciences is an Open Access journal and articles published are distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC). Readers may copy, distribute, and display the work for non-commercial purposes with the proper citation of the original work.

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Neurosciences Journal: 15 (4)
Neurosciences Journal
Vol. 15, Issue 4
1 Oct 2010
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Allicin can reduce neuronal death and ameliorate the spatial memory impairment in Alzheimers disease models
Xian-Hui Li, Chun-Yan Li, Zhi-Gang Xiang, Fei Zhong, Zheng-Ying Chen, Jiang-Ming Lu
Neurosciences Journal Oct 2010, 15 (4) 237-243;

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Allicin can reduce neuronal death and ameliorate the spatial memory impairment in Alzheimers disease models
Xian-Hui Li, Chun-Yan Li, Zhi-Gang Xiang, Fei Zhong, Zheng-Ying Chen, Jiang-Ming Lu
Neurosciences Journal Oct 2010, 15 (4) 237-243;
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© 2025 Neurosciences Journal Neurosciences is copyright under the Berne Convention and the International Copyright Convention. All rights reserved. Neurosciences is an Open Access journal and articles published are distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC). Readers may copy, distribute, and display the work for non-commercial purposes with the proper citation of the original work. Electronic ISSN 1658-3183. Print ISSN 1319-6138.

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