Protective effects of transfecting bone morphogenetic protein-7 on rat cardiomyocytes against hypoxia-reoxygenation injury
- VernacularTitle:rrBMP-7基因对缺氧复氧损伤心肌细胞的保护作用
- Author:
Jihong XU
;
Junke WANG
;
Zhiguo YUAN
- Publication Type:Journal Article
- Keywords:
bone morphogenetic protein 7;
transfection;
reperfusion injury
- From:
Medical Journal of Chinese People's Liberation Army
2001;0(11):-
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the protective effect of transfecting bone morphogenetic protein-7 (BMP-7) on cultured neonatal rat cardiomyocytes against hypoxia-reoxygenation injury. Methods Neonatal rat cardiomyocytes were cultured. The pcDNA-rrBMP7 was introduced into cardiomyocytes by Fugene 6.0 transfection method. The cardiomyocytes were divided into three groups: control group (group C), hypoxia-reoxygenation group (group HR) and gene transfecting group (group BT). Trypan blue exclusion test was performed to detect cell viability. The activity of lactate dehydrogenase (LDH) and creatine phosphokinase (CPK) was assayed to evaluate cell injury. For evaluating the cell antioxidant ability, the activity of superoxide dismutase (SOD) and the level of malondialdehyde (MDA) were determined by colorimetric assay. Fluo-3 labeling method and confocal laser scanning microscopy were used to observe the change in intracellular calcium. Results The results showed that after 120 min of simulated ischemia followed by 240 min of reperfusion, cell pulsation rate was decreased, the activity of LDH, CPK and the trypan blue uptake rate were increased. As compared with the group C, SOD activity decreased and the content of MDA increased in Group HR. Compared with Group HR, the SOD activity increased and the content of MDA decreased in group BT. Treatment with BMP-7 gene transfecting led to a decrease of i content in cardiomyocytes, showing that overloading of i induced by hypoxia-reoxygenation was prevented (P
