Qian Z M, Xu M F, Tang P L
Department of Applied Biology and Chemical Technology, Hong Kong Polytechnic University, Hung Hom, Kowloon.
Free Radic Res. 1997 Jul;27(1):13-21. doi: 10.3109/10715769709097833.
The effect of superoxide dismutase (SOD) on membrane integrity and fluidity of the cultured neonatal rat cardiac myocytes in vitro was investigated under the condition of hypoxia and hypoxia/reoxygenation. Lactate dehydrogenase (LDH) concentration was used as the biochemical indicator for the loss of cell membrane integrity. Fluorescence polarization (FP), average microviscosity (eta) and anisotropy (Ast), which are inversely proportional to the fluidity of cell membrane, were assayed. Cells were respectively exposed to hypoxia or hypoxia/reoxygenation for different periods of time in the absence or presence of SOD at various concentrations. Hypoxia alone or hypoxia/reoxygenation brought injury to the cultured myocytes. This was demonstrated by changes in LDH and membrane fluidity. In the former LDH concentration gradually increased in a time-dependent manner and the values of FP, eta and Ast were significantly increased. The changes in membrane integrity and fluidity induced by hypoxia or hypoxia/reoxygenation could be prevented by adding SOD to the culture medium. The results provide a direct evidence that SOD (740 u.ml-1, the effective dose) was effective in protecting cultured myocytes against the injury as well as an indirect evidence of free radical generation. Based on the results obtained from this study and the establishment of concept of optimally effective dose by Bernier and Omar et al, it was suggested that some previous reports, in which no evidence was found both in protective effect of SOD and in free radical generation by using only one dose in hypoxia/reoxygenation model, should be interpreted with caution.
在缺氧及缺氧/复氧条件下,研究了超氧化物歧化酶(SOD)对体外培养的新生大鼠心肌细胞的膜完整性及膜流动性的影响。以乳酸脱氢酶(LDH)浓度作为细胞膜完整性丧失的生化指标。检测了与细胞膜流动性呈反比的荧光偏振(FP)、平均微黏度(η)和各向异性(Ast)。在不同浓度SOD存在或不存在的情况下,将细胞分别暴露于缺氧或缺氧/复氧不同时间段。单纯缺氧或缺氧/复氧均对培养的心肌细胞造成损伤,这通过LDH及膜流动性的变化得以证实。在前一种情况下,LDH浓度随时间呈逐渐增加,而FP、η和Ast值显著升高。向培养基中添加SOD可预防由缺氧或缺氧/复氧引起的膜完整性及膜流动性的变化。结果提供了直接证据,表明SOD(740 u.ml-1,有效剂量)能有效保护培养的心肌细胞免受损伤,同时也提供了自由基生成的间接证据。基于本研究结果以及Bernier和Omar等人建立的最佳有效剂量概念,提示对一些既往报道应谨慎解读,这些报道在缺氧/复氧模型中仅使用单一剂量时,未发现SOD的保护作用及自由基生成的证据。