钾离子通道在糖尿病及其并发症中的重要作用

Channels (Austin, Tex.) Pub Date : 2025-12-01 Epub Date: 2025-07-12 DOI:10.1080/19336950.2025.2531949
Xiangdong Yang, Yan Yang
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引用次数: 0

摘要

钾离子通道(K+ channel)是存在于细胞膜上的一种重要的跨膜蛋白,在调节细胞膜电位、动作电位形成和细胞兴奋性等多种生理过程中起着关键作用。糖尿病是一种以血糖水平升高为特征的慢性代谢紊乱,随着时间的推移,会导致K+通道的敏感性和功能发生异常变化。这可能导致细胞内K+和Ca2+的增加,破坏正常的细胞功能和代谢,并导致一系列生理和代谢问题。最近的研究揭示了K+通道辅助性SUR1和Kir6.2门控之间的协同关系,以及K+通道突变如KCNK11 Leu114Pro、KCNQ1Arg397Trp、KCNJ11Arg136Cys、KCNK16 Leu114Pro和KCNMA1 Gly356Arg对糖尿病及相关并发症的影响。特别强调了诸如心脏复极受损、KATP、Kir、TALK和KV通道重构以及心律失常的高风险等问题。此外,结构性和功能失调的K+通道(KCa、KV和Kir)也会影响血管内皮细胞和平滑肌细胞的功能,导致血管运动功能受损、细胞生长异常和炎症增加。这些异常可导致心血管损伤和病变,并增加糖尿病患者患心血管疾病的风险。这些发现为更好地理解和解决糖尿病患者的心血管问题奠定了重要的基础。此外,针对K+通道的不同药物和治疗可能产生不同的效果,为预防和控制糖尿病及其相关并发症提供了广阔的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The crucial role of potassium ion channels in diabetes mellitus and its complications: A review.

Potassium ion channel (K+ channel) is a crucial transmembrane protein found on cell membranes that plays a pivotal role in regulating various physiological processes such as cell membrane potential, action potential formation, and cellular excitability. Diabetes, a chronic metabolic disorder characterized by elevated blood glucose levels, can cause abnormal changes in the sensitivity and functioning of K+ channels over time. This can lead to an increase in intracellular K+ and Ca2+, disrupting normal cellular function and metabolism and resulting in a range of physiological and metabolic issues. Recent studies have uncovered the collaborative relationship between K+ channels auxiliary SUR1 and Kir6.2 gating, as well as the impact of K+ channel mutations such as KCNK11 Leu114Pro, KCNQ1Arg397Trp, KCNJ11Arg136Cys, KCNK16 Leu114Pro, and KCNMA1 Gly356Arg on diabetes mellitus and associated complications. Specifically, issues such as impaired cardiac repolarization, KATP, Kir, TALK, and KV channel remodeling and a higher risk of arrhythmia have been emphasized. Furthermore, structural and dysfunctional K+ channels (KCa, KV and Kir) can also affect the function of vascular endothelial and smooth muscle cells, leading to impaired vasomotor function, abnormal cell growth, and increased inflammation. These abnormalities can result in cardiovascular damage and lesions, and increase the risk of cardiovascular disease in diabetic individuals. These findings serve as a crucial foundation for a better understanding and addressing cardiovascular issues in patients with diabetes. Moreover, different drugs and treatments targeting the K+ channel may yield varying effects, offering promising prospects for preventing and managing diabetes and its related complications.

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