Pink1 基因:2 型糖尿病病理生理学中的关键角色

IF 0.7 Q4 PHARMACOLOGY & PHARMACY Egyptian Pharmaceutical Journal Pub Date : 2024-07-08 DOI:10.4103/epj.epj_51_24
Khuzin Dinislam, Pozdnyakov Egor, Hezheva Arina, Kirill Sergienko, Sharonova Anastasia, Melissa Rumyantseva, Margarita Smurygina, Surkova Svetlana, Abid Ali, M. A. Khoso
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引用次数: 0

摘要

2 型糖尿病(T2DM)是一种复杂的代谢疾病,伴有胰岛素抵抗和葡萄糖代谢不良。新的证据表明,PTEN 诱导的假定激酶 1(Pink1)在疾病进展中具有重要意义。Pink1 编码一种蛋白激酶,可调节和维持线粒体的活性,主要影响有丝分裂和能量生成。Pink1 基因突变与氧化应激、线粒体功能失调和细胞能量输出受损有关。胰岛素抵抗和 T2DM 的出现可能都是由这些特征引起的。为了了解 Pink1 在糖尿病发病过程中的潜在功能,本综述论文研究了 Pink1 影响葡萄糖代谢和胰岛素信号传导的分子机制。根据临床前研究,有可能开发出专门针对 Pink1 的创新治疗策略。这些策略的目的是调节胰岛素抵抗,改善葡萄糖代谢,保护糖尿病患者的β细胞功能。以下研究领域包括弄清 Pink1 在糖尿病中的确切功能、将临床前研究结果转化为临床环境、探索专门针对 Pink1 的精准医疗方法,以及确定 Pink1 通路中可能的治疗靶点。本综述旨在加深我们对 Pink1 对 T2DM 影响的理解,并开发针对代谢紊乱的个性化疗法。此外,它还强调了坚持这类研究以加强糖尿病治疗策略的意义。
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Pink1 gene: a key player in the pathophysiology of type 2 diabetes mellitus
Type 2 diabetes mellitus (T2DM) is a complicated metabolic condition with insulin resistance and poor glucose metabolism. Emerging evidence indicates the significance of (PTEN-induced putative kinase 1 (Pink1) in the progression of diseases. Pink1 encodes a protein kinase, which regulates and maintains mitochondrial activity, this mostly affects mitophagy and energy generation. Mutations in the Pink1 gene have been associated to oxidative stress, mitochondrial malfunction, and impaired cellular energy output. The presence of insulin resistance and T2DM may be caused by each of these characteristics. To understand Pink1 potential function in the development of diabetes, this review paper investigates the molecular mechanisms through which it influences glucose metabolism and insulin signaling. Based on preclinical investigations, there is potential for developing innovative therapeutic strategies that specifically target Pink1. These strategies could aim to regulate insulin resistance, improve glucose metabolism, and preserve beta-cell function among individuals diagnosed with diabetes. The following areas of research include figuring out how precisely Pink1 functions in diabetes, translating preclinical findings into clinical settings, exploring precision medicine approaches that specifically target Pink1, and identifying possible therapeutic targets within the Pink1 pathway. This review aims to enhance our understanding of Pink1 impact on T2DM and develop personalized treatments for metabolic disorders. Furthermore, it underscores the significance of persisting with this type of investigation to enhance diabetes treatment strategies.
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来源期刊
Egyptian Pharmaceutical Journal
Egyptian Pharmaceutical Journal PHARMACOLOGY & PHARMACY-
CiteScore
1.10
自引率
0.00%
发文量
37
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