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首页> 外文期刊>American Journal of Physiology >Effects of elevated physiological temperatures on sarcoplasmic reticulum function in mechanically skinned muscle fibers of the rat.
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Effects of elevated physiological temperatures on sarcoplasmic reticulum function in mechanically skinned muscle fibers of the rat.

机译:生理温度升高对大鼠机械剥皮的肌纤维中肌浆网功能的影响。

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Properties of the sarcoplasmic reticulum (SR) with respect to Ca(2+) loading and release were measured in mechanically skinned fiber preparations from isolated extensor digitorum longus (EDL) muscles of the rat that were either kept at room temperature (23 degrees C) or exposed to temperatures in the upper physiological range for mammalian skeletal muscle (30 min at 40 or 43 degrees C). The ability of the SR to accumulate Ca(2+) was significantly reduced by a factor of 1.9-2.1 after the temperature treatments due to a marked increase in SR Ca(2+) leak, which persisted for at least 3 h after treatment. Results with blockers of Ca(2+) release channels (ruthenium red) and SR Ca(2+) pumps [2,5-di(tert-butyl)-1,4-hydroquinone] indicate that the increased Ca(2+) leak was not through the SR Ca(2+) release channel or the SR Ca(2+) pump, although it is possible that the leak pathway was via oligomerized Ca(2+) pump molecules. No significant change in the maximum SR Ca(2+)-ATPase activity was observed after the temperature treatment, although there was a tendency for a decrease in the SR Ca(2+)-ATPase. The observed changes in SR properties were fully prevented by the superoxide (O(2)(*-)) scavenger Tiron (20 mM), indicating that the production of O(2)(*-) at elevated temperatures is responsible for the increase in SR Ca(2+) leak. Results show that physiologically relevant elevated temperatures 1) induce lasting changes in SR properties with respect to Ca(2+) handling that contribute to a marked increase in the SR Ca(2+) leak and, consequently, to the reduction in the average coupling ratio between Ca(2+) transport and SR Ca(2+)-ATPase and muscle performance, and 2) that these changes are mediated by temperature-induced O(2)(*-) production.
机译:肌浆网(SR)相对于Ca(2+)负载和释放的特性是通过机械剥皮的纤维制备物制成的,该纤维制备物来自大鼠的孤立的指趾长肌(EDL)肌肉,或者保持在室温(23摄氏度)或暴露于哺乳动物骨骼肌的较高生理范围内的温度下(在40或43摄氏度下30分钟)。温度处理后,由于SR Ca(2+)泄漏显着增加,SR累积Ca(2+)的能力显着降低了1.9-2.1倍,在处理后至少持续3小时。 Ca(2+)释放通道(钌红)和SR Ca(2+)泵[2,5-二(叔丁基)-1,4-对苯二酚]的阻滞结果表明增加的Ca(2+)泄漏不是通过SR Ca(2+)释放通道或SR Ca(2+)泵,尽管泄漏途径可能是通过低聚Ca(2+)泵分子。尽管有减少SR Ca(2 +)-ATPase的趋势,但在温度处理后未观察到最大SR Ca(2 +)-ATPase活性的显着变化。超氧化物(O(2)(*-))清除剂Tiron(20 mM)完全阻止了SR特性的观察到的变化,表明在高温下O(2)(*-)的产生是增加的原因SR Ca(2+)泄漏。结果表明,生理上相关的高温1)引起SR特性相对于Ca(2+)处理的持久变化,从而导致SR Ca(2+)泄漏显着增加,因此导致平均耦合降低Ca(2+)运输与SR Ca(2 +)-ATPase和肌肉性能之间的比率,以及2)这些变化是由温度诱导的O(2)(*-)生产介导的。

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