Abstract
The capacity of cornel iridoid glycoside (CIG) to suppress the manifestations of ischemic stroke was investigated. CIG was administered to rats by the intragastric route once daily for 7 days. Focal cerebral ischemia was induced by 2 h of middle cerebral artery occlusion followed by 24 h of reperfusion. In non-treated rats large infarct areas were observed within 24 h of reperfusion. Examination of the ischemic cerebral cortex revealed microglia and astrocyte activation, increased interleukin-1β (IL-1 β) and tumor necrosis factor-α (TNF-α) concentrations, increased DNA fragmentation in the ischemia penumbra, elevated Bax expression, increased caspase-3 cleavage, and decreased Bcl-2 expression. Pretreatment with CIG decreased the infarct area, DNA fragmentation, IL-1β and TNF-α concentrations, microglia and astrocyte activation, Bax expression, and caspase-3 cleavage while increasing Bcl-2 expression. CIG exerts anti-neuroinflammatory and anti-apoptotic effects which should prove beneficial for prevention or treatment of stroke.
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Acknowledgments
This study was supported by the National Key Basic Research 973 Program of China (Grant No. 2003CB517104), the National Natural Science Foundation of China (Grant No. 90709011, 30973513), and the Beijing Municipal Science and Technology Program of China (Grant No. D0206001043191).
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Ya, Bl., Li, Cy., Zhang, L. et al. Cornel Iridoid Glycoside Inhibits Inflammation and Apoptosis in Brains of Rats with Focal Cerebral Ischemia. Neurochem Res 35, 773–781 (2010). https://doi.org/10.1007/s11064-010-0134-2
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DOI: https://doi.org/10.1007/s11064-010-0134-2