The Impact of Chronic Magnesium Deficiency on Excitable Tissues-Translational Aspects.

IF 3.4 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Biological Trace Element Research Pub Date : 2025-02-01 Epub Date: 2024-05-06 DOI:10.1007/s12011-024-04216-2
Marija Stanojević, Nadezda Djuricic, Miro Parezanovic, Marko Biorac, Dhruba Pathak, Svetolik Spasic, Srdjan Lopicic, Sanjin Kovacevic, Jelena Nesovic Ostojic
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Abstract

Neuromuscular excitability is a vital body function, and Mg2+ is an essential regulatory cation for the function of excitable membranes. Loss of Mg2+ homeostasis disturbs fluxes of other cations across cell membranes, leading to pathophysiological electrogenesis, which can eventually cause vital threat to the patient. Chronic subclinical Mg2+ deficiency is an increasingly prevalent condition in the general population. It is associated with an elevated risk of cardiovascular, respiratory and neurological conditions and an increased mortality. Magnesium favours bronchodilation (by antagonizing Ca2+ channels on airway smooth muscle and inhibiting the release of endogenous bronchoconstrictors). Magnesium exerts antihypertensive effects by reducing peripheral vascular resistance (increasing endothelial NO and PgI2 release and inhibiting Ca2+ influx into vascular smooth muscle). Magnesium deficiency disturbs heart impulse generation and propagation by prolonging cell depolarization (due to Na+/K+ pump and Kir channel dysfunction) and dysregulating cardiac gap junctions, causing arrhythmias, while prolonged diastolic Ca2+ release (through leaky RyRs) disturbs cardiac excitation-contraction coupling, compromising diastolic relaxation and systolic contraction. In the brain, Mg2+ regulates the function of ion channels and neurotransmitters (blocks voltage-gated Ca2+ channel-mediated transmitter release, antagonizes NMDARs, activates GABAARs, suppresses nAChR ion current and modulates gap junction channels) and blocks ACh release at neuromuscular junctions. Magnesium exerts multiple therapeutic neuroactive effects (antiepileptic, antimigraine, analgesic, neuroprotective, antidepressant, anxiolytic, etc.). This review focuses on the effects of Mg2+ on excitable tissues in health and disease. As a natural membrane stabilizer, Mg2+ opposes the development of many conditions of hyperexcitability. Its beneficial recompensation and supplementation help treat hyperexcitability and should therefore be considered wherever needed.

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长期缺镁对可兴奋组织的影响--翻译方面。
神经肌肉的兴奋性是人体的一项重要功能,而 Mg2+ 是调节兴奋膜功能的重要阳离子。Mg2+ 失衡会扰乱其他阳离子在细胞膜上的通量,导致病理生理电生,最终对患者造成重大威胁。慢性亚临床 Mg2+ 缺乏症在普通人群中越来越普遍。它与心血管、呼吸系统和神经系统疾病风险升高以及死亡率增加有关。镁有利于支气管扩张(通过拮抗气道平滑肌上的 Ca2+ 通道和抑制内源性支气管收缩剂的释放)。镁通过降低外周血管阻力(增加内皮 NO 和 PgI2 的释放,抑制 Ca2+ 流入血管平滑肌)发挥降压作用。缺镁通过延长细胞去极化(由于 Na+/K+ 泵和 Kir 通道功能障碍)和调节心脏间隙连接失调来干扰心脏冲动的产生和传播,从而导致心律失常,同时延长舒张期 Ca2+ 释放(通过泄漏的 RyRs)干扰心脏兴奋-收缩耦合,损害舒张期松弛和收缩期收缩。在大脑中,Mg2+ 可调节离子通道和神经递质的功能(阻断电压门控 Ca2+ 通道介导的递质释放、拮抗 NMDARs、激活 GABAARs、抑制 nAChR 离子电流和调节缝隙连接通道),并阻断神经肌肉接头处的 ACh 释放。镁具有多种治疗神经活性作用(抗癫痫、抗偏头痛、镇痛、神经保护、抗抑郁、抗焦虑等)。本综述将重点讨论 Mg2+ 对健康和疾病中可兴奋组织的影响。作为一种天然的膜稳定剂,Mg2+ 能抑制许多过度兴奋情况的发生。它的有益补偿和补充有助于治疗过度兴奋,因此在需要时应加以考虑。
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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来源期刊
Biological Trace Element Research
Biological Trace Element Research 生物-内分泌学与代谢
CiteScore
8.70
自引率
10.30%
发文量
459
审稿时长
2 months
期刊介绍: Biological Trace Element Research provides a much-needed central forum for the emergent, interdisciplinary field of research on the biological, environmental, and biomedical roles of trace elements. Rather than confine itself to biochemistry, the journal emphasizes the integrative aspects of trace metal research in all appropriate fields, publishing human and animal nutritional studies devoted to the fundamental chemistry and biochemistry at issue as well as to the elucidation of the relevant aspects of preventive medicine, epidemiology, clinical chemistry, agriculture, endocrinology, animal science, pharmacology, microbiology, toxicology, virology, marine biology, sensory physiology, developmental biology, and related fields.
期刊最新文献
Correction to: Resveratrol Mitigates Cerebral Ischemic Injury by Altering Levels of Trace Elements, Toxic Metal, Lipid Peroxidation, and Antioxidant Activity. Retraction Note: Assessment of Titanium Dioxide Nanoparticles (TiO2-NPs) Induced Hepatotoxicity andAmeliorative Effects of Cinnamomum cassia in Sprague-Dawley Rats. Research on the Effect and Mechanism of Selenium on Colorectal Cancer Through TRIM32. The Impact of Chronic Magnesium Deficiency on Excitable Tissues-Translational Aspects. Mechanisms of Heavy Metal Cadmium (Cd)-Induced Malignancy.
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