Flanagan S W, Moseley P L, Buettner G R
Department of Exercise Science, The University of Iowa, Iowa City 52242, USA.
FEBS Lett. 1998 Jul 17;431(2):285-6. doi: 10.1016/s0014-5793(98)00779-0.
It has been hypothesized that hyperthermia promotes oxygen-centered free radical formation in cells; however, to date there is no direct evidence of this heat-induced increase in oxygen free radical flux. Using electron paramagnetic resonance (EPR) spin trapping, we sought direct evidence for free radical generation during hyperthermia in intact, functioning cells. Rat intestinal epithelial cell monolayers were exposed to 45 degrees C for 20 min, after which the nitrone spin trap 5,5-dimethyl-1-pyrroline N-oxide (DMPO) was added. Compared to control cells at 37 degrees C, heat-exposed cells had increased free radical EPR signals, consistent with the formation of DMPO/.OH (aN = aH = 14.9 G). These findings indicate that heat increases the flux of cellular free radicals and support the hypothesis that increased generation of oxygen-centered free radicals and the resultant oxidative stress may mediate in part, heat-induced cellular damage.
有假说认为,热疗会促进细胞中以氧为中心的自由基形成;然而,迄今为止,尚无直接证据表明热诱导的氧自由基通量增加。我们使用电子顺磁共振(EPR)自旋捕获技术,寻找在完整的、有功能的细胞热疗过程中自由基生成的直接证据。将大鼠肠上皮细胞单层暴露于45摄氏度20分钟,之后加入硝酮自旋捕获剂5,5-二甲基-1-吡咯啉N-氧化物(DMPO)。与37摄氏度的对照细胞相比,热暴露细胞的自由基EPR信号增加,这与DMPO/.OH(aN = aH = 14.9 G)的形成一致。这些发现表明,热会增加细胞自由基通量,并支持以下假说:以氧为中心的自由基生成增加以及由此产生的氧化应激可能部分介导热诱导的细胞损伤。