Suppr超能文献

钠-葡萄糖协同转运蛋白2抑制剂疗法与间歇性禁食在心肾综合征中的作用:葡萄糖介导的氧化应激的作用

Sodium-Glucose-Cotransporter-2 Inhibitor Therapy and Intermitted Fasting in Cardiorenal Syndrome: The Role of Glucose-Mediated Oxidative Stress.

作者信息

Schröder Katrin

机构信息

Institute of Cardiovascular Physiology, Medical Faculty, Goethe University, 60590 Frankfurt, Germany.

German Center of Cardiovascular Research (DZHK), Partner Site Rhein-Main, 60590 Frankfurt, Germany.

出版信息

J Clin Med. 2025 Jan 24;14(3):746. doi: 10.3390/jcm14030746.

Abstract

Cardiorenal syndrome (CRS) is a complex clinical disorder characterized by the interplay between heart and kidney dysfunction. This condition is exacerbated by comorbidities such as diabetes mellitus, which contribute to glucose-mediated oxidative stress, further complicating the management of CRS. The management of CRS has evolved with the discovery of sodium-glucose-cotransporter-2 (SGLT2) inhibitors, which have been established as effective agents in reducing hyperglycemia and demonstrated cardiorenal protective effects. Concurrently, intermittent fasting has gained attention as an intervention without pharmacological treatment for its metabolic benefits, including improved glucose metabolism and insulin regulation and sensitivity, both with a potential reduction in oxidative stress. This review provides a summary of current findings on the roles of SGLT2 inhibitors and intermittent fasting in managing CRS, with a particular focus on glucose-mediated oxidative stress. We evaluate the mechanisms by which these interventions exert their effects, identify gaps in current research, and offer recommendations for future studies. While both SGLT2 inhibitors and intermittent fasting demonstrate potential in managing CRS, more research is needed to elucidate their long-term efficacy, safety, and potential synergistic effects.

摘要

心肾综合征(CRS)是一种复杂的临床病症,其特征为心脏和肾脏功能障碍之间的相互作用。糖尿病等合并症会加剧这种情况,糖尿病会导致葡萄糖介导的氧化应激,使CRS的管理更加复杂。随着钠-葡萄糖协同转运蛋白-2(SGLT2)抑制剂的发现,CRS的管理方式发生了演变,SGLT2抑制剂已被确认为降低高血糖的有效药物,并显示出心肾保护作用。与此同时,间歇性禁食作为一种无需药物治疗的干预措施因其代谢益处而受到关注,这些益处包括改善葡萄糖代谢、胰岛素调节和敏感性,同时有可能降低氧化应激。本综述总结了目前关于SGLT2抑制剂和间歇性禁食在管理CRS中的作用的研究结果,特别关注葡萄糖介导的氧化应激。我们评估了这些干预措施发挥作用的机制,确定了当前研究中的差距,并为未来研究提供了建议。虽然SGLT2抑制剂和间歇性禁食在管理CRS方面都显示出潜力,但仍需要更多研究来阐明它们的长期疗效、安全性和潜在的协同作用。

相似文献

2
Cardiorenal Syndrome in Type 2 Diabetes Mellitus - Rational Use of Sodium-glucose Cotransporter-2 Inhibitors.
Eur Endocrinol. 2020 Oct;16(2):113-121. doi: 10.17925/EE.2020.16.2.113. Epub 2020 Oct 6.
4
An Overview of the Cardiorenal Protective Mechanisms of SGLT2 Inhibitors.
Int J Mol Sci. 2022 Mar 26;23(7):3651. doi: 10.3390/ijms23073651.
5
Cardiorenal protection of SGLT2 inhibitors-Perspectives from metabolic reprogramming.
EBioMedicine. 2022 Sep;83:104215. doi: 10.1016/j.ebiom.2022.104215. Epub 2022 Aug 13.
7
8
Potential Underlying Mechanisms Explaining the Cardiorenal Benefits of Sodium-Glucose Cotransporter 2 Inhibitors.
Adv Ther. 2024 Jan;41(1):92-112. doi: 10.1007/s12325-023-02652-5. Epub 2023 Nov 9.
9
SGLT2 inhibitors in the treatment of type 2 cardiorenal syndrome: Focus on renal tubules.
Front Nephrol. 2023 Jan 12;2:1109321. doi: 10.3389/fneph.2022.1109321. eCollection 2022.

引用本文的文献

1
Vitamin D Deficiency and Its Role in Pathologies of Oxidative Stress: A Literature Review.
Cureus. 2025 Aug 13;17(8):e90042. doi: 10.7759/cureus.90042. eCollection 2025 Aug.

本文引用的文献

1
From fasting to fat reshaping: exploring the molecular pathways of intermittent fasting-induced adipose tissue remodeling.
J Pharm Pharm Sci. 2024 Jul 22;27:13062. doi: 10.3389/jpps.2024.13062. eCollection 2024.
2
SGLT2i effect on atrial fibrillation: A network meta-analysis of randomized controlled trials.
J Cardiovasc Electrophysiol. 2024 Sep;35(9):1754-1765. doi: 10.1111/jce.16344. Epub 2024 Jun 28.
3
Specific signaling by nicotinamide adenine dinucleotide oxidases - Role of their site of action.
Curr Opin Chem Biol. 2024 Aug;81:102461. doi: 10.1016/j.cbpa.2024.102461. Epub 2024 May 28.
4
Study Examines Intermittent Fasting and Cardiovascular Mortality.
JAMA. 2024 May 7;331(17):1440. doi: 10.1001/jama.2024.5158.
5
Targeting inflammatory signaling pathways with SGLT2 inhibitors: Insights into cardiovascular health and cardiac cell improvement.
Curr Probl Cardiol. 2024 May;49(5):102524. doi: 10.1016/j.cpcardiol.2024.102524. Epub 2024 Mar 16.
6
The Effect of Fasting on Cardiovascular Diseases: A Systematic Review.
Cureus. 2024 Jan 30;16(1):e53221. doi: 10.7759/cureus.53221. eCollection 2024 Jan.
8
Intermittent fasting protects β-cell identity and function in a type-2 diabetes model.
Metabolism. 2024 Apr;153:155813. doi: 10.1016/j.metabol.2024.155813. Epub 2024 Feb 1.
9
Effects of SGLT2 Inhibitors and DPP-4 Inhibitors on Advanced Glycation End Products.
Drug Res (Stuttg). 2024 Feb;74(2):77-80. doi: 10.1055/a-2234-1797. Epub 2024 Jan 29.
10
Arachidonic acid inhibition of the NLRP3 inflammasome is a mechanism to explain the anti-inflammatory effects of fasting.
Cell Rep. 2024 Feb 27;43(2):113700. doi: 10.1016/j.celrep.2024.113700. Epub 2024 Jan 23.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验