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Ca(2+)-dependent regulation of the Ca(2+) concentration in the myometrium mitochondria. II. Ca(2+) effects on mitochondria membranes polarization and Ca(2+)(m)

机译:Ca(2 +) - 依赖于肌瘤线粒体中Ca(2+)浓度的调节。 II。 Ca(2+)对线粒体膜极化的影响和Ca(2 +)(m)

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摘要

It is known that Ca2+ accumulation in the mitochondria undergoes complex regulation by Ca2+ itself. But the mechanisms of such regulation are still discussed. In this paper we have shown that Ca ions directly or indirectly regulate the level of myometrium mitochondria membranes polarization. The additions of 100 µM Ca2+ were accompanied by depolarization of the mitochondria membranes. The following experiments were designed to study the impact of Ca2+ on the myometrium mitochondria [Ca2+]m. Isolated myometrium mitochondria were preincubated without or with 10 μM Са2+ followed by 100 μM Са2+ addition. Experiments were conducted in three mediums: without ATP and Mg2+ (0-medium), in the presence of 3 mM Mg2+ (Mg-medium) and 3 mM Mg2+ + 3 mM ATP (Mg,ATP-medium). It was shown that the effects of 10 μM Са2+ addition were different in different mediums, namely in 0- and Mg-medium the [Ca2+]m values increased, whereas in Mg,ATP-medium statistically reliable changes were not registered. Preincubation of mitochondria with 10 μM Са2+ did not affect the [Ca2+]m value after the addition of 100 μM Са2+. The [Ca2+]m values after 100 μM Са2+ addition were the same in 0- and Mg,ATP-mediums and somewhat lower in Mg-medium. Preliminary incubation of mitochondria with 10 μM Са2+ in 0- and Mg-mediums reduced changes of Fluo 4 normalized fluorescence values that were induced by 100 μM Са2+ additions, but in Mg,ATP-medium such differences were not recorded. It is concluded that Са2+ exchange in myometrium mitochondria is regulated by the concentration of Ca ions as in the external medium, so in the matrix of mitochondria. The medium composition had a significant impact on the [Са2+]m values in the absence of exogenous cation. It is suggested that light increase of [Са2+]m before the addition of 100 μM Са2+ may have a positive effect on the functional activity of the mitochondria.
机译:众所周知,线粒体中的Ca2 +积累经历了Ca2 +本身的复杂调节。但仍然讨论了这种规范的机制。在本文中,我们表明Ca离子直接或间接调节肌瘤线粒体膜膜极化水平。 100μMCa2+的添加伴随着线粒体膜的去极化。设计了以下实验,研究了Ca2 +对肌瘤线粒体的影响[Ca2 +] m的影响。分离的肌瘤线粒体预孵育,没有或用10μmса2+,然后达到100μmСа2+加入。实验在三种培养基中进行:没有ATP和Mg2 +(0-培养基),在3mM Mg 2 +(Mg-培养基)和3mM Mg 2 + + 3mm ATP(Mg,ATP培养基)存在下。结果表明,在不同培养基中,10μmСа2+加入的效果不同,即在0-和mg-培养基中,[Ca2 +] m值增加,而在Mg中,未注册ATP介质统计上可靠的变化。用10μmСа2+的线粒体预孵育不影响添加100μmСа2+后的[Ca2 +] m值。 100μmСа2+加入后的[Ca2 +] m值在0-和mg,ATP培养基中的相同,在Mg-培养基中略低。用10μmСа2+的线粒体促进0-和Mg-培养基的氟化荧光型荧光值的变化降低了100μmСа2+添加的荧光荧光值,但在Mg中,未记录ATP培养基的差异。结论是,肌瘤线粒体中的Са2+交换由如外部介质中的Ca离子浓度调节,因此在线粒体基质中。培养基组合物在没有外源阳离子的情况下对α2m值产生显着影响。建议在添加100μmСа2+之前[са2+] m的光增加可能对线粒体的功能活性产生积极影响。

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