三碘甲状腺原氨酸对约束小鼠皮质、海马和小脑线粒体H +、ca2 +和Mg 2+依赖离子转运体的快速作用

S. Simi, K. Manish, M. Peter
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引用次数: 0

摘要

甲状腺激素(TH)具有多种作用,主要与生命早期的发育和分化有关,在包括神经组织在内的几乎所有组织中都起着重要作用。TH通过其基因组和直接作用于线粒体结合位点迅速改变线粒体功能。哺乳动物应激反应中TH与线粒体离子转运的功能关系尚不清楚。在这里,我们报道了三碘甲状腺原氨酸(t3)对短期服用三碘甲状腺原氨酸(t3)的瑞士白化小鼠(小脑)皮质、海马和小脑神经元簇线粒体离子转运蛋白功能的快速体内作用。200ng g-1),无应激或抑制应激(每天30分钟,连续7天)。非应激和抑制应激小鼠的皮质mH + - atp酶活性在t3治疗后均显著降低。相反,非应激和抑制应激小鼠海马和小脑的mH + - atp酶活性在t3处理后均显著升高。非应激和抑制应激小鼠的皮质和小脑mCa 2+ - atp酶活性在t3治疗后均显著降低。海马mCa 2+ - atp酶活性在t3处理后显著升高,在t3处理小鼠抑制应激后出现逆转。抑制应激小鼠经t3处理后,皮质线粒体Mg 2+ - atp酶活性显著降低。相反,t3处理使小鼠小脑线粒体Mg 2+ - atp酶活性显著升高。非应激小鼠海马线粒体Mg 2+ - atp酶活性在t3处理后显著升高,而t3处理抑制应激小鼠海马线粒体Mg 2+ - atp酶活性逆转。在本研究中发现了t3对线粒体离子转运体的空间和差异作用,证实了t3对小鼠脑线粒体中H +、ca2 +和mg2 +转运的快速调节作用,这似乎对约束应激敏感。
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Rapid action of Triiodothyronine on Mitochondrial H + , Ca 2+ and Mg 2+ -Dependent ion Transporters in Cortex, Hippocampus and Cerebellum of Restraint Mice
Thyroid hormones (TH) have a multitude of actions, mainly on development and differentiation during early life and play many vital roles in almost all tissues including neuronal tissues. TH rapidly alters the mitochondrial functions both by its genomic and direct actions on mitochondrial binding sites. The functional relationship between TH and mitochondrial ion transport during stress response has not yet been elucidated in mammals so far. Here, we report a rapid in vivo action of triiodothyronine (T 3 ) on mitochondrial ion transporter functions in the neuronal clusters of cortex, hippocampus and cerebellum of Swiss Albino mouse ( Mus musculus ) treated short-term with triiodothyronine (T 3 ; 200ng g-1) for 30 min either in non-stressed or in restraint-stressed (30 min each day for 7 days). The mH + -ATPase activity in the cortex decreased to significant levels after T 3 treatment in both non-stressed and restraint-stressed mice. On the contrary, the mH + -ATPase activity in the hippocampus and cerebellum increased to significant levels after T 3 treatment in both non-stressed and restraint-stressed mice. The mCa 2+ -ATPase activity in the cortex and cerebellum decreased to significant levels after T 3 treatment in both non-stressed and restraint-stressed mice. The mCa 2+ -ATPase activity in the hippocampus that increased to significant levels after T 3 treatment, showed a reversal after restraint-stress in T 3 -treated mice. The mitochondrial Mg 2+ -ATPase activity in the cortex decreased to significant levels after T 3 treatment in restraint-stressed mice. On the contrary, T 3 treatment in restraint stressed mice increased to significant levels the mitochondrial Mg 2+ -ATPase activity in the cerebellum. The mitochondrial Mg 2+ -ATPase activity in the hippocampus, which increased to significant levels after T 3 treatment in non-stressed mice, reversed its activity in T 3 -treated restraint-stressed mice. Spatial and differential action of T 3 on the mitochondrial ion transporters has been found in the present study that corroborates with a rapid modulatory action of T 3 on the transport of H + , Ca 2+ and Mg 2+ in the brain mitochondria of mice which appears to be sensitive to restraint stress.
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