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Differing Effects of Cyclosporin A on Swelling Amplitude and Time Constant of Mitochondria from Normal and Ischemic Rat Brain

机译:环孢菌素A对正常和缺血大鼠脑线粒体肿胀幅度和时间常数的不同影响

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The purpose of this study was to investigate the effect of cyclosporin A on swelling amplitude and time constant of mitochondria isolated from normal and ischemic rat brain and to observe the possible role of the mitochondrial ATP-sensitive potassium channel on mitochondrial permeability transition. Mitochondrial swelling was evaluated by spectrophotometry. Cyclosporin A at 0.5 or 1 microM and diazoxide at 30 microM significantly decreased the swelling amplitude and attenuated the reduction of time constant of mitochondria isolated from normal brain mitochondria induced by 200 microM calcium, an effect abolished by atractyloside at 100 microM. However, cyclosporin A at 5 microM did not affect mitochondrial swelling. In mitochondria from ischemic brain, cyclosporin A at 0.5 microM but not 1 microM significantly decreased mitochondrial swelling amplitude and attenuated the reduction of time constant, which was abolished by atractyloside. Diazoxide had an effect similar to cyclosporin A at 0.5 microM, which was blocked by atractyloside or 5-hydroxydecanoate at 100 microM and 200 microM. Compared with mitochondria isolated from normal brain, those from ischemic brain were more sensitive to cyclosporin A. Activation of the mitochondrial ATP-sensitive potassium channel may be one of the mechanisms by which opening of the mitochondrial permeability transition pore is inhibited
机译:本研究的目的是研究环孢菌素A对正常和缺血大鼠脑线粒体溶胀幅度和时间常数的影响,并观察线粒体ATP敏感性钾通道对线粒体通透性转变的可能作用。通过分光光度法评估线粒体肿胀。 0.5或1 microM的环孢菌素A和30 microM的二氮嗪显着降低了溶胀幅度,并减弱了由200 microM钙诱导的从正常脑线粒体中分离出的线粒体的时间常数,这一作用在100 microM时被白术甙所废止。但是,环孢菌素A的浓度为5 microM不会影响线粒体肿胀。在缺血性脑的线粒体中,环孢菌素A的浓度为0.5 microM,而不是1 microM,则显着降低了线粒体的溶胀幅度,并减弱了时间常数的减小,这一作用被白术苷所废止。二氮嗪在0.5 microM时具有类似于环孢菌素A的作用,在100 microM和200 microM时被白术苷或5-羟基癸酸酯所阻断。与从正常脑中分离出的线粒体相比,从缺血性脑中分离出的线粒体对环孢菌素A更敏感。线粒体ATP敏感性钾通道的激活可能是抑制线粒体通透性转换孔开放的机制之一。

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