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Effect of Xueshuantong and Ginsenoside Rd on lipopolysaccharides actived microglia cells
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DOI   10.11656/j.issn.1673-9043.2015.06.07
Key Words   Xueshuantong;nitric oxide;inflammatory mediator;microglia
Author NameAffiliationE-mail
YANG Hong-yun Key Laboratory of Pharmacology of Traditional Chinese Medical Formulae, Ministry of Education, Tianjin Key Laboratory of Chinese medicine Pharmacology, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China  
LIU Xiao-lei Key Laboratory of Pharmacology of Traditional Chinese Medical Formulae, Ministry of Education, Tianjin Key Laboratory of Chinese medicine Pharmacology, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China  
CHAI Li-juan Key Laboratory of Pharmacology of Traditional Chinese Medical Formulae, Ministry of Education, Tianjin Key Laboratory of Chinese medicine Pharmacology, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China  
WANG Shao-xia Key Laboratory of Pharmacology of Traditional Chinese Medical Formulae, Ministry of Education, Tianjin Key Laboratory of Chinese medicine Pharmacology, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China wangshaoxia1978@hotmail.com 
HU Li-min Key Laboratory of Pharmacology of Traditional Chinese Medical Formulae, Ministry of Education, Tianjin Key Laboratory of Chinese medicine Pharmacology, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China  
Abstract
    [Objective] To study the effects of Xueshuantong and its monomer on actived microglia (BV-2) and its mechanism. [Methods] The experiment was divided into control group, lipopolysaccharide(LPS) group, dosing group and positive control group (mino), detecting of Xueshuantong (different dilution multiples of Xueshuantong and its monomer composition) to the vitality of microglia and nitric oxide(NO) induced by LPS using the Greiss method. [Results] Between 0.5~50 μg/mL, Xueshuantong could not inhibit the microglia release NO induced by LPS, among the 5 kinds of monomer composition of Xueshuantong, ginsenoside Rg1, Rb1, Re and Notoginsenoside could not inhibit the microglia release NO induced by LPS, however, ginsenoside Rd could inhibit NO secretion without affecting the cell vitality, and inhibit the mRNA expression of iNOS, IL-1β, IL-6. [Conclusion] The monomer composition of ginsenoside Rd in Xueshuangtong can inhibit activated microglia release NO and the mRNA of iNOS,IL-1β,IL-6 significantly. It may be one of neural protection mechanism.

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