Cellular and Mitochondrial Pathways Contribute to SGLT2 Inhibitors-mediated Tissue Protection: Experimental and Clinical Data

线粒体 计算生物学 细胞生物学 生物 化学 医学
作者
Raúl Sanz,Sebastián García Menéndez,Felipe Inserra,León Ferder,Walter Manucha
出处
期刊:Current Pharmaceutical Design [Bentham Science Publishers]
卷期号:30 (13): 969-974 被引量:4
标识
DOI:10.2174/0113816128289350240320063045
摘要

Abstract: In metabolic syndrome and diabetes, compromised mitochondrial function emerges as a critical driver of cardiovascular disease, fueling its development and persistence, culminating in cardiac remodeling and adverse events. In this context, angiotensin II - the main interlocutor of the renin-angiotensin-aldosterone system - promotes local and systemic oxidative inflammatory processes. To highlight, the low activity/expression of proteins called sirtuins negatively participates in these processes, allowing more significant oxidative imbalance, which impacts cellular and tissue responses, causing tissue damage, inflammation, and cardiac and vascular remodeling. The reduction in energy production of mitochondria has been widely described as a significant element in all types of metabolic disorders. Additionally, high sirtuin levels and AMPK signaling stimulate hypoxia-inducible factor 1 beta and promote ketonemia. Consequently, enhanced autophagy and mitophagy advance through cardiac cells, sweeping away debris and silencing the orchestra of oxidative stress and inflammation, ultimately protecting vulnerable tissue from damage. To highlight and of particular interest, SGLT2 inhibitors (SGLT2i) profoundly influence all these mechanisms. Randomized clinical trials have evidenced a compelling picture of SGLT2i emerging as game-changers, wielding their power to demonstrably improve cardiac function and slash the rates of cardiovascular and renal events. Furthermore, driven by recent evidence, SGLT2i emerge as cellular supermolecules, exerting their beneficial actions to increase mitochondrial efficiency, alleviate oxidative stress, and curb severe inflammation. Its actions strengthen tissues and create a resilient defense against disease. In conclusion, like a treasure chest brimming with untold riches, the influence of SGLT2i on mitochondrial function holds untold potential for cardiovascular health. Unlocking these secrets, like a map guiding adventurers to hidden riches, promises to pave the way for even more potent therapeutic strategies.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
sh完成签到,获得积分10
1秒前
qqqqqqq完成签到,获得积分10
1秒前
xwydx发布了新的文献求助10
1秒前
apo发布了新的文献求助10
1秒前
Ming完成签到,获得积分10
1秒前
2秒前
Nivas完成签到,获得积分10
2秒前
2秒前
xuli发布了新的文献求助10
2秒前
酷波er应助简单千秋采纳,获得10
3秒前
4秒前
雪白语琴发布了新的文献求助10
4秒前
茂飞发布了新的文献求助10
5秒前
热情初瑶发布了新的文献求助10
5秒前
5秒前
5秒前
Dawang发布了新的文献求助10
5秒前
勇敢的风完成签到,获得积分10
5秒前
橙橙完成签到,获得积分10
6秒前
6秒前
6秒前
6秒前
wang发布了新的文献求助10
6秒前
miles发布了新的文献求助10
7秒前
7秒前
8秒前
lmy发布了新的文献求助10
8秒前
kuoping完成签到,获得积分0
9秒前
9秒前
9秒前
orixero应助橙橙采纳,获得10
9秒前
arya发布了新的文献求助10
10秒前
10秒前
NexusExplorer应助yiling采纳,获得10
11秒前
小白发布了新的文献求助10
11秒前
小叶子发布了新的文献求助50
11秒前
xuli完成签到,获得积分10
12秒前
十二应助czy采纳,获得10
12秒前
简单千秋发布了新的文献求助10
12秒前
在水一方应助超威蓝猫采纳,获得10
12秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Principles of town planning: translating concepts to applications 1000
2016 Venous Blood Study (VBS) (Final V3.0) 510
Management and the Arts 510
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
The Effective Clinical Neurologist 3ed 500
The Great Hymn to Šamaš 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7699388
求助须知:如何正确求助?哪些是违规求助? 9258701
关于积分的说明 20015754
捐赠科研通 7274521
什么是DOI,文献DOI怎么找? 3293487
关于科研通互助平台的介绍 2448934
邀请新用户注册赠送积分活动 2299794