Aging Leads to Over-Expression of Na+/K+ Pump Units in Liver and Na+/Ca2+ Exchangers in Brain Cortex

A. Nikoghosyan, Armenuhi Heqimyan, S. Ayrapetyan
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引用次数: 1

Abstract

The metabolic controlling of tissue hydration is the fundamental parameter determining cell functional activity and its dysfunction is the common consequence of any cell pathology, including aging. The aim of the present study is to reveal the differences of age-dependent metabolic controlling of cell hydration of excitable tissue such as brain cortex and non-excitable tissues such as liver and spleen. For this purpose, the age-dependent sensitivity of cell hydration in excitable and non-excitablet issues is studied through depressing metabolic activity by cooling and its activation by supplying animals with distilled water, by inactivation of Na+/K+ pump and activation of Na+/Ca2+ exchange in the reverse mode. The obtained data bring us to the conclusion that the metabolic regulation of cell hydration in excitable tissue is realized by the activation of electrogenic Na+/K+ pump and Na+/Ca2+ exchange in the cell membrane and the formation of endogen water by mitochondrial activity, while the regulation of cell hydration in non-excitable tissue is carried out only by the activity of mitochondrial function. Aging leads to an over-expression of Na+/K+ pump units in liver and Na+/Ca2+ exchanger in brain cortex of rats.
衰老导致肝脏中Na+/K+泵单位和脑皮质中Na+/Ca2+交换器的过度表达
组织水合作用的代谢控制是决定细胞功能活性的基本参数,其功能障碍是包括衰老在内的任何细胞病理学的常见后果。本研究的目的是揭示大脑皮层等易兴奋组织与肝脏和脾脏等非易兴奋组织细胞水合作用的年龄依赖性代谢控制的差异。为此,通过冷却抑制代谢活性和向动物供应蒸馏水激活代谢活性,通过Na+/K+泵失活和反向激活Na+/Ca2+交换,研究了细胞水合作用在兴奋性和非兴奋性问题中的年龄依赖性敏感性。所获得的数据使我们得出结论,可兴奋组织中细胞水合作用的代谢调节是通过激活细胞膜中的生电Na+/K+泵和Na+/Ca2+交换以及线粒体活性形成内源性水来实现的,而非兴奋性组织中细胞水合作用的调节仅通过线粒体功能的活性来进行。衰老导致大鼠肝脏中Na+/K+泵单元和大脑皮层中Na+/Ca2+交换器的过度表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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