3 results match your criteria: "Department of Pathophysiology of North China Coal Medical College[Affiliation]"
Zhongguo Ying Yong Sheng Li Xue Za Zhi
November 2007
Department of Pathophysiology of North China Coal Medical College, Tangshan 063000, China.
Aim: To probe into the affection and significance of NO on the expression of P-selectin in renal injury following hind limb ischemia/reperfusion in rats.
Methods: In accordance with the conventional approaches of our department, the model rats were prepared after they were made to undergo 4 hours or ischemia followed by 4 hours of reperfusion of hind limbs. The Wistar rats were divided into four groups randomly: Control group, LI/R group, L-Arg group and L-NAME group.
Zhongguo Ying Yong Sheng Li Xue Za Zhi
November 2005
Department of Pathophysiology of North China Coal Medical College, Tangshan, 063000, China.
Aim: To study the effects of PKC activation on apoptosis during ischemia/reperfusion in L-6TG rat skeletal myoblasts.
Methods: Cultured L-6TG cells were divided into 3 groups: control group (C), ischemia/reperfusion group (I/R), PMA + ischemia/ reperfusion group (PMA), SOD, XOD and free calcium and mitochondrial respiration in L-6TG cell were evaluated in each group. Apoptosis was detected by flow cytometer with PI staining method and agarose gel electrophoresis, the immunohistochemical method was used to determine the expression of caspase-3.
Zhongguo Ying Yong Sheng Li Xue Za Zhi
August 2005
Department of Pathophysiology of North China Coal Medical College, Tangshan 063000, China.
Aim: To establish a model of ischemia/reperfusion injury on L-6TG cell.
Methods: Cultured L-6TG cells were divided into 2 groups: control group (C), ischemia/reperfusion group (I/R), LDH in culture fluid, SOD, XOD, free calcium in L-6TG cell and mitochondria respiration were evaluated in each group, the micromorphologic changes were observed with microscope.
Results: Compared with control group, after L-6TG cell suffered ischemia 4 hours and reperfusion 4 hours, LDH in culture fluid, XOD, free calcium in L-6TG cell all increased significantly, while SOD in L-6TG cell and mitochondrial respiration decreased, structural damage to L-6TG cell was severe.