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Some in vitro experiments have shown that erythropoietin(EPO) increases resistance to apoptosis and facilitates neuronal survival following cerebral ischemia.However,results from in vivo studies are rarely reported.Perfusion-weighted imaging(PWI) and diffusion-weighted imaging(DWI) have been applied successfully to distinguish acute cerebral ischemic necrosis and penumbra in living animals; therefore,we hypothesized that PWI and DWI could be used to provide imaging evidence in vivo for the conclusion that EPO could reduce apoptosis in brain areas injured by cerebral ischemia/reperfusion.To validate this hypothesis,we established a rat model of focal cerebral ischemia/reperfusion injury,and treated with intra-cerebroventricular injection of EPO(5,000 U/kg) 20 minutes before injury.Brain tissue in the ischemic injury zone was sampled using MRI-guided localization.The relative area of abnormal tissue,changes in PWI and DWI in the ischemic injury zone,and the number of apoptotic cells based on Td T-mediated d UTP-biotin nick end-labeling(TUNEL) were assessed.Our findings demonstrate that EPO reduces the relative area of abnormally high signal in PWI and DWI,increases cerebral blood volume,and decreases the number of apoptotic cells positive for TUNEL in the area injured by cerebral ischemia/reperfusion.The experiment provides imaging evidence in vivo for EPO treating cerebral ischemia/reperfusion injury.
Some in vitro experiments have shown that erythropoietin (EPO) increases resistance to apoptosis and facilitates neuronal survival following cerebral ischemia. However, results from in vivo studies are rarely reported. Perfusion-weighted imaging (PWI) and diffusion-weighted imaging (DWI) have had applied successfully to distinguish acute cerebral ischemic necrosis and penumbra in living animals; therefore, we hypothesized that PWI and DWI could be used to provide imaging evidence in vivo for the conclusion that EPO could reduce apoptosis in brain areas injured by cerebral ischemia / reperfusion. To validate this hypothesis, we established a rat model of focal cerebral ischemia / reperfusion injury, and treated with intra-cerebroventricular injection of EPO (5,000 U / kg) for 20 minutes before injury. Brain tissue in the ischemic injury zone was sampled using MRI- guided localization. the relative area of abnormal tissue, changes in PWI and DWI in the ischemic injury zone, and the number of apoptotic cells base Our findings demonstrate that EPO reduces the relative area of abnormally high signal in PWI and DWI, increases cerebral blood volume, and decreases the number of apoptotic cells positive for TUNEL in the area injured by cerebral ischemia / reperfusion. The experiment provides imaging evidence in vivo for EPO treated cerebral ischemia / reperfusion injury.