哺乳动物细胞水合作用的量子力学敏感性

A. Nikoghosyan, Lilia Narinyan, Armenuhi Heqimyan, S. Ayrapetyan
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引用次数: 2

摘要

阐明弱化学和弱物理因子对细胞和生物体的生物学作用机理是生命科学的现代课题之一。根据Bernard Katz教授的受体理论,生物物质对细胞的影响是通过激活膜上的配体门控离子通道来实现的。然而,这一理论并不能很好地解释不同化学物质在极低浓度下产生的类似生物效应,这些化学物质不能激活膜内的离子通道,对细胞具有非线性的剂量依赖性。以前我们已经提出细胞水合作用的代谢控制可以作为一种通用的量子力学传感器,用于各种弱的物理和化学信号。为了支持这一假设,本文比较研究了低浓度冷(非放射性)和[3H]-瓦巴因(Na+/K+- atp酶特异性抑制剂)对大鼠不同组织水化的影响。所获得的数据表明,冷和[3H]-瓦巴因对细胞水化的影响是不同的,这种差异取决于组织的初始代谢状态。基于我们之前和现在的结果,我们认为这种细胞水化的量子力学敏感性是通过环核苷酸依赖的Na+/Ca2+交换来实现的,在细胞水化的代谢调节中起着至关重要的作用。
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The Quantum-Mechanical Sensitivity of Cell Hydration in Mammals
The elucidation of the mechanism on the biological effects of weak chemical and physical factors on cells and organism is one of the modern problems in life sciences. According to the Receptor Theory of Prof. Bernard Katz the impact of the biological substances on cells is realized through the activation of ligand-gated ion channels in the membrane. However, this theory doesn’t provide a satisfactory explanation on the similar biological effects of extremely low concentrations of different chemical substances, which are unable to activate the ionic channels in the membrane and have non-linear dose-dependent effect on cells. Previously we have suggested that the metabolic control of cell hydration serves as a universal quantum-mechanical sensor for different weak physical and chemical signals. For supporting this hypothesis, in this article the comparative study of the effects of low concentrations of both cold (non-radioactive) and [3H]-ouabain (specific inhibitor for Na+/K+-ATPase) on the hydration in different tissues of rats has been performed. The obtained data have shown that cold and [3H]-ouabain have different effects on cell hydration and such a difference depends on the initial metabolic state of tissues. On the basis of our previous and present results it is suggested that such a quantum-mechanical sensitivity of cell hydration is realized through the cyclic-nucleotides-dependent Na+/Ca2+ exchange, having a crucial role in the metabolic regulation of cell hydration.
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