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Sestrin2作为高血压的潜在靶点

Sestrin2 as a Potential Target in Hypertension.

作者信息

Didik Steven, Wang Hao, James Adewale Segun, Slotabec Lily, Li Ji

机构信息

Department of Surgery, University of South Florida, Tampa, FL 33612, USA.

James A. Haley Veterans' Hospital, Tampa, FL 33612, USA.

出版信息

Diagnostics (Basel). 2023 Jul 14;13(14):2374. doi: 10.3390/diagnostics13142374.

Abstract

Hypertension is a highly complex, intricate condition affecting millions of individuals across the globe. Nearly half of adults in the United States are diagnosed with hypertension, with incident rates projected to rise over the next decade. Hypertension is a precursor to many cardiovascular diseases including atherosclerosis, stroke, myocardial infarction, heart failure, and peripheral artery disease. This review describes the major processes contributing to the development of hypertension and how Sestrin2 (Sesn2), an antioxidative protein, could be a potential target in the treatment of hypertension. In hypertension, increased reactive oxygen species (ROS) production is a critical component in the etiology of the condition. The increased ROS in hypertension is derived from a variety of sources, all of which are covered in depth in this review. Increased ROS is generated from mitochondrial stress, endoplasmic reticulum (ER) stress, NADPH oxidase (NOX) overactivity, and the uncoupling of endothelial nitric oxidase synthase (eNOS). Sesn2, a highly conserved, stress-inducible protein, has the structural and functional characteristics to be a potential therapeutic target to alleviate the progression of hypertension. The structure, function, genetics, and characteristics of Sesn2 are presented in the review. The Nrf2/Sesn2, Sesn2/AMPK/mTOR, and Sesn2/Angiotensin II signaling pathways are described in detail in this review. Sesn2 can be utilized in a multitude of ways as a therapeutic modality in hypertension. This review explores potential Sesn2 inducers and activators and how Sesn2 can be incorporated into gene therapy for the treatment of hypertension.

摘要

高血压是一种高度复杂、错综复杂的病症,影响着全球数百万人。在美国,近一半的成年人被诊断患有高血压,预计在未来十年发病率还会上升。高血压是许多心血管疾病的先兆,包括动脉粥样硬化、中风、心肌梗死、心力衰竭和外周动脉疾病。本综述描述了导致高血压发展的主要过程,以及抗氧化蛋白Sestrin2(Sesn2)如何可能成为治疗高血压的潜在靶点。在高血压中,活性氧(ROS)生成增加是该病症病因中的关键因素。高血压中ROS增加源自多种来源,本综述将对所有这些来源进行深入探讨。ROS增加是由线粒体应激、内质网(ER)应激、NADPH氧化酶(NOX)过度活跃以及内皮型一氧化氮合酶(eNOS)解偶联产生的。Sesn2是一种高度保守、应激诱导的蛋白质,具有成为缓解高血压进展的潜在治疗靶点的结构和功能特征。本综述介绍了Sesn2的结构、功能、遗传学和特性。本综述详细描述了Nrf2/Sesn2、Sesn2/AMPK/mTOR和Sesn2/血管紧张素II信号通路。Sesn2可以通过多种方式用作高血压的治疗手段。本综述探讨了潜在的Sesn2诱导剂和激活剂,以及Sesn2如何可以纳入基因治疗以治疗高血压。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a75a/10378131/be18ea8c8304/diagnostics-13-02374-g001.jpg

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