Protective Effect of Resveratrol Pretreatment on Cerebral Ischemic Reperfusion Damage in Rats
Jian Qian, Xiaochen Yang, Chen MuLan, Ren ZiJian, Jun Guo
Abstract
Jian Qian, Xiaochen Yang, Chen MuLan, Ren ZiJian, Jun Guo
Abstract
Objective: To study on the neuroprotection of resveratrol (Res) pretreatment against injury of cerebral ischemic reperfusion (I/R) in rats and study the molecular mechanism of Res against I/R injury. Methods: The rats are divided into three groups randomly, i.e. sham group, I/R (DMSO) group and Res pretreatment group. The global brain ischemia model was constructed with 4-VO occlusion method. After ischemia of 10min /reperfusion of 22h, test the SOD activity and the content of NO, MDA in the hippocampus tissue with kits. The expression of GRP78 was investigated with RT-PCR. Results: The SOD activity in ischemia group was obviously lower than sham group, the content of NO, MDA was higher than sham group; The SOD activity and the content of NO, MDA induced by ischemia could be reversed significantly after Res preconditioning. Ischemia evidently up-regulating the expression of GRP78, the Res pretreatment can effectually inhibit the expression of GRP78 induced by ischemia. Conclusion: Resveratrol can cut off the way of free radicals' production and accumulation through a mechanism which can up-regulate the SOD activity and inhibit the content of NO and MDA. Accordingly this releases the endoplasmic reticulum stress and lowers the expression of GRP78, weakening cerebral ischemia damage.
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Objective: To study on the neuroprotection of resveratrol (Res) pretreatment against injury of cerebral ischemic reperfusion (I/R) in rats and study the molecular mechanism of Res against I/R injury. Methods: The rats are divided into three groups randomly, i.e. sham group, I/R (DMSO) group and Res pretreatment group. The global brain ischemia model was constructed with 4-VO occlusion method. After ischemia of 10min /reperfusion of 22h, test the SOD activity and the content of NO, MDA in the hippocampus tissue with kits. The expression of GRP78 was investigated with RT-PCR. Results: The SOD activity in ischemia group was obviously lower than sham group, the content of NO, MDA was higher than sham group; The SOD activity and the content of NO, MDA induced by ischemia could be reversed significantly after Res preconditioning. Ischemia evidently up-regulating the expression of GRP78, the Res pretreatment can effectually inhibit the expression of GRP78 induced by ischemia. Conclusion: Resveratrol can cut off the way of free radicals' production and accumulation through a mechanism which can up-regulate the SOD activity and inhibit the content of NO and MDA. Accordingly this releases the endoplasmic reticulum stress and lowers the expression of GRP78, weakening cerebral ischemia damage.
Key concepts: Ischemia, Resveratrol, Neuroprotection, Pharmacology, Hippocampus, Reperfusion injury, Endoplasmic reticulum, Medicine