Trending toward gero-electroceuticals that target membrane potential for reprogramming aging and lifespan

Siamak Tabibzadeh, Olen R. Brown
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Abstract

Ion gradients across cell membranes generate voltage potentials that are involved in a wide range of biological processes. According to the membrane hypothesis of aging, aging is inextricably linked to a decrease in resting membrane potential (Vmem). Alterations in ion channel activity and membrane fluidity caused by aging disrupt bioelectric homeostasis, increase intracellular calcium and potassium concentrations, induce abnormal mechanistic target of rapamycin (MTOR)- and AMPK-regulated metabolism and energy dissipation, and decrease proliferation and regeneration. Failure to maintain ion channel activity and membrane potential leads to cell senescence or death. There is evidence that by manipulating ion channel activities, a cryptic memory can be recalled to restore lost proliferative or regenerative abilities. Reversal or prevention of senescence, aging phenotypes, and longevity may be achieved by fine-tuning mitochondrial membrane polarization. Therefore, there is optimism that deciphering the bioelectric codes that govern cell functions will lead to the development of new gero-electroceuticals that restore cell function and prevent tissue loss during aging.

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以膜电位为目标的老年电疗药物是重塑衰老和寿命的大势所趋
细胞膜上的离子梯度会产生电压电位,这些电压电位与多种生物过程有关。根据膜衰老假说,衰老与静息膜电位(Vmem)的降低密不可分。衰老引起的离子通道活性和膜流动性的改变会破坏生物电平衡,增加细胞内钙和钾的浓度,诱发雷帕霉素机制靶标(MTOR)和 AMPK 调节的新陈代谢和能量消耗异常,并减少增殖和再生。无法维持离子通道活性和膜电位会导致细胞衰老或死亡。有证据表明,通过操纵离子通道活性,可以唤醒隐性记忆,恢复失去的增殖或再生能力。通过微调线粒体膜极化,可以逆转或防止衰老、老化表型和长寿。因此,人们乐观地认为,破译细胞功能的生物电密码将开发出新的老年电疗药物,以恢复细胞功能并防止衰老过程中的组织损失。
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