The role of pyruvate metabolism in cardiovascular diseases.

IF 3.8 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Zijie Cheng, Haoqi Li, Dan Wu, Qingxun Hu
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引用次数: 0

Abstract

Cardiovascular diseases remain the leading cause of mortality worldwide, with their incidence steadily rising in recent years. Pyruvate, the end product of glycolysis, serves as a critical metabolite in cellular energy metabolism by bridging cytoplasmic glycolysis and mitochondrial oxidative phosphorylation. Its synthesis, transport, and metabolic conversion are tightly regulated by a range of enzymes and transporters, including pyruvate kinase, mitochondrial pyruvate carriers, pyruvate dehydrogenase complex, glucose transporters, and lactate dehydrogenase. Emerging evidence suggests that dysregulation of pyruvate metabolism plays a pivotal role in the pathogenesis of various cardiovascular conditions, including heart failure, ischemia-reperfusion injury, diabetic cardiomyopathy, and pulmonary hypertension. This review aimed to provide a comprehensive and integrative overview of the role of pyruvate metabolism in cardiovascular diseases by systematically analyzing recent findings from both experimental and clinical studies. Unlike previous reviews that focus on isolated enzymes or specific disease types, we adopted a systemic perspective to elucidate the entire pyruvate metabolic network and its crosstalk with mitochondrial function, redox homeostasis, and inflammatory signaling pathways. We also discuss the regulatory roles of key signaling cascades, such as PI3K-AKT, and the implications of genetic variations in enzymes involved in pyruvate metabolism. Finally, we highlight potential molecular targets within this pathway that could be leveraged for therapeutic intervention. By mapping these interconnections, our review underscores the therapeutic potential of targeting pyruvate metabolism as a novel strategy for treating cardiovascular disorders. SIGNIFICANCE STATEMENT: Pyruvate metabolism plays a crucial role in cardiovascular disease development and has attracted growing interest. While previous reviews have examined enzymes like PDC and PKM2, they often focus narrowly on specific pathways or disease types. This review offers a more integrated, system-level perspective, highlighting the roles of pyruvate metabolism in mitochondrial function, redox balance, and inflammation. It also identifies potential metabolic targets, aiming to support future therapeutic strategies in treating cardiovascular conditions.

丙酮酸代谢在心血管疾病中的作用。
心血管疾病仍然是世界范围内死亡的主要原因,近年来其发病率稳步上升。丙酮酸是糖酵解的最终产物,通过桥接细胞质糖酵解和线粒体氧化磷酸化,是细胞能量代谢的关键代谢物。它的合成、运输和代谢转化受到一系列酶和转运蛋白的严格调控,包括丙酮酸激酶、线粒体丙酮酸载体、丙酮酸脱氢酶复合物、葡萄糖转运蛋白和乳酸脱氢酶。越来越多的证据表明,丙酮酸代谢失调在各种心血管疾病的发病机制中起着关键作用,包括心力衰竭、缺血再灌注损伤、糖尿病性心肌病和肺动脉高压。本文旨在通过系统分析最近的实验和临床研究结果,对丙酮酸代谢在心血管疾病中的作用进行全面和综合的综述。不同于以往的综述关注于分离酶或特定疾病类型,我们采用了系统的观点来阐明整个丙酮酸代谢网络及其与线粒体功能、氧化还原稳态和炎症信号通路的相互作用。我们还讨论了关键信号级联的调节作用,如PI3K-AKT,以及参与丙酮酸代谢的酶的遗传变异的含义。最后,我们强调了这一途径中可能用于治疗干预的潜在分子靶点。通过绘制这些相互联系,我们的综述强调了靶向丙酮酸代谢作为治疗心血管疾病的新策略的治疗潜力。意义声明:丙酮酸代谢在心血管疾病的发展中起着至关重要的作用,并引起了越来越多的关注。虽然以前的综述已经研究了PDC和PKM2等酶,但它们通常只关注特定的途径或疾病类型。这篇综述提供了一个更完整的系统水平的观点,强调了丙酮酸代谢在线粒体功能、氧化还原平衡和炎症中的作用。它还确定了潜在的代谢靶点,旨在支持未来治疗心血管疾病的治疗策略。
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
CiteScore
6.90
自引率
0.00%
发文量
115
审稿时长
1 months
期刊介绍: A leading research journal in the field of pharmacology published since 1909, JPET provides broad coverage of all aspects of the interactions of chemicals with biological systems, including autonomic, behavioral, cardiovascular, cellular, clinical, developmental, gastrointestinal, immuno-, neuro-, pulmonary, and renal pharmacology, as well as analgesics, drug abuse, metabolism and disposition, chemotherapy, and toxicology.
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