2005Unpublished venueRequires access

Nalxone decreases the ratio of apoptosis of the rabbit’s hippocampus cells induced by ischemia and reperfusion

Jian Wu

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Abstract

Objective:To study the protective effect of Nalonxe on the hippocampus cells of rabbits induced by ischemia and reperfusion. Methods:20 New Zealand white rabbits were randomly divided in four groups: control group, ischemia (bilateral common carotid artery and vertebral artery were occluded for 30mins) group, ischemia-reperfusion(above mentioned occluded artery were opened for 6hours) group, reperfusion associated with Naloxone therapy(0.8mg/kg iv and then 0.3mg/kg vd.) group. At the end of intervention, the ratio of apoptosis of hippocampus cells were assayed by flow cytometry. Results:1.The ratio of apoptosis of ischemia group and ischemia-reperfusion group were all significant higher than control group(P0.01 respectively); and the ratio of ischemia-reperfusion group was significant higher than ischemia and naloxone group(P0.01 respectively). (2. There) was no remarkable difference between that of naloxone therapy group and control group.Conclusion:Ischemia and ischemia-reperfusion may lead to apoptosis of hippocampus cells. Naloxone significantly reduces apoptosis of hippocampus cells and provide protective effect on hypoxia and reperfusion injure.

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Objective:To study the protective effect of Nalonxe on the hippocampus cells of rabbits induced by ischemia and reperfusion. Methods:20 New Zealand white rabbits were randomly divided in four groups: control group, ischemia (bilateral common carotid artery and vertebral artery were occluded for 30mins) group, ischemia-reperfusion(above mentioned occluded artery were opened for 6hours) group, reperfusion associated with Naloxone therapy(0.8mg/kg iv and then 0.3mg/kg vd.) group. At the end of intervention, the ratio of apoptosis of hippocampus cells were assayed by flow cytometry. Results:1.The ratio of apoptosis of ischemia group and ischemia-reperfusion group were all significant higher than control group(P0.01 respectively); and the ratio of ischemia-reperfusion group was significant higher than ischemia and naloxone group(P0.01 respectively). (2. There) was no remarkable difference between that of naloxone therapy group and control group.Conclusion:Ischemia and ischemia-reperfusion may lead to apoptosis of hippocampus cells. Naloxone significantly reduces apoptosis of hippocampus cells and provide protective effect on hypoxia and reperfusion injure.

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Available abstract

Objective:To study the protective effect of Nalonxe on the hippocampus cells of rabbits induced by ischemia and reperfusion. Methods:20 New Zealand white rabbits were randomly divided in four groups: control group, ischemia (bilateral common carotid artery and vertebral artery were occluded for 30mins) group, ischemia-reperfusion(above mentioned occluded artery were opened for 6hours) group, reperfusion associated with Naloxone therapy(0.8mg/kg iv and then 0.3mg/kg vd.) group. At the end of intervention, the ratio of apoptosis of hippocampus cells were assayed by flow cytometry. Results:1.The ratio of apoptosis of ischemia group and ischemia-reperfusion group were all significant higher than control group(P0.01 respectively); and the ratio of ischemia-reperfusion group was significant higher than ischemia and naloxone group(P0.01 respectively). (2. There) was no remarkable difference between that of naloxone therapy group and control group.Conclusion:Ischemia and ischemia-reperfusion may lead to apoptosis of hippocampus cells. Naloxone significantly reduces apoptosis of hippocampus cells and provide protective effect on hypoxia and reperfusion injure.

Key concepts: Ischemia, Apoptosis, Medicine, Hippocampus, Anesthesia, Reperfusion injury, (+)-Naloxone, Hypoxia (environmental)

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