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Title: Ginsenosides attenuate kainic acid-induced synaptosomal oxidative stress via stimulation of adenosine A(2A) receptors in rat hippocampus. Author: Shin EJ, Koh YH, Kim AY, Nah SY, Jeong JH, Chae JS, Kim SC, Yen TP, Yoon HJ, Kim WK, Ko KH, Kim HC. Journal: Behav Brain Res; 2009 Jan 30; 197(1):239-45. PubMed ID: 18809438. Abstract: Treatment with ginsenosides attenuated KA-induced seizures and oxidative stress in the synaptosome, and reduced synaptic vesicles at the presynaptic terminals dose-dependently. The adenosine A(2A) receptor antagonist 1,3,7-trimethyl-8-(3-chlorostyryl) xanthine reversed the ginsenoside-mediated pharmacological actions. Neither the adenosine A(1) receptor antagonist 8-cyclopentyl-1,3-dimethylxanthine nor the adenosine A(2B) receptor antagonist alloxazine affected the ginsenoside-mediated pharmacological actions. Our results suggest that ginsenosides block KA-induced synaptosomal oxidative stress, associated with hippocampal degeneration, through activation of adenosine A(2A) receptors.[Abstract] [Full Text] [Related] [New Search]