Literature DB >> 34328095

New progress in drugs treatment of diabetic kidney disease.

Junmin Wang1, Hongjiao Xiang1, Yifei Lu1, Tao Wu2, Guang Ji3.   

Abstract

Diabetic kidney disease (DKD) is not only one of the main complications of diabetes, but also the leading cause of the end-stage renal disease (ESRD). The occurrence and development of DKD have always been a serious clinical problem that leads to the increase of morbidity and mortality and the severe damage to the quality of life of human beings. Controlling blood glucose, blood pressure, blood lipids, and improving lifestyle can help slow the progress of DKD. In recent years, with the extensive research on the pathological mechanism and molecular mechanism of DKD, there are more and more new drugs based on this, such as new hypoglycemic drugs sodium-glucose cotransporter 2 (SGLT2) inhibitors, glucagon-like peptide-1 (GLP-1) inhibitors, and dipeptidyl peptidase-4 (DPP-4) inhibitors with good efficacy in clinical treatment. Besides, there are some newly developed drugs, including protein kinase C (PKC) inhibitors, advanced glycation end product (AGE) inhibitors, aldosterone receptor inhibitors, endothelin receptor (ETR) inhibitors, transforming growth factor-β (TGF-β) inhibitors, Rho kinase (ROCK) inhibitors and so on, which show positive effects in animal or clinical trials and bring hope for the treatment of DKD. In this review, we sort out the progress in the treatment of DKD in recent years, the research status of some emerging drugs, and the potential drugs for the treatment of DKD in the future, hoping to provide some directions for clinical treatment of DKD.
Copyright © 2021 The Authors. Published by Elsevier Masson SAS.. All rights reserved.

Entities:  

Keywords:  Diabetic kidney disease; New drugs; Treatment

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Year:  2021        PMID: 34328095     DOI: 10.1016/j.biopha.2021.111918

Source DB:  PubMed          Journal:  Biomed Pharmacother        ISSN: 0753-3322            Impact factor:   6.529


  4 in total

1.  Proteomic Analysis of Mouse Kidney Tissue Associates Peroxisomal Dysfunction with Early Diabetic Kidney Disease.

Authors:  Aggeliki Tserga; Despoina Pouloudi; Jean Sébastien Saulnier-Blache; Rafael Stroggilos; Irene Theochari; Harikleia Gakiopoulou; Harald Mischak; Jerome Zoidakis; Joost Peter Schanstra; Antonia Vlahou; Manousos Makridakis
Journal:  Biomedicines       Date:  2022-01-20

2.  Network Meta-Analysis on the Effects of SGLT2 Inhibitors Versus Finerenone on Cardiorenal Outcomes in Patients With Type 2 Diabetes and Chronic Kidney Disease.

Authors:  Li-Min Zhao; Ze-Lin Zhan; Jie Ning; Mei Qiu
Journal:  Front Pharmacol       Date:  2022-01-24       Impact factor: 5.810

3.  Paeoniflorin directly binds to TNFR1 to regulate podocyte necroptosis in diabetic kidney disease.

Authors:  Xian Wang; Xue-Qi Liu; Ling Jiang; Yue-Bo Huang; Han-Xu Zeng; Qi-Jin Zhu; Xiang-Ming Qi; Yong-Gui Wu
Journal:  Front Pharmacol       Date:  2022-09-06       Impact factor: 5.988

4.  KITLG Promotes Glomerular Endothelial Cell Injury in Diabetic Nephropathy by an Autocrine Effect.

Authors:  Jiun-Chi Huang; Szu-Chia Chen; Wei-An Chang; Wei-Wen Hung; Ping-Hsun Wu; Ling-Yu Wu; Jer-Ming Chang; Ya-Ling Hsu; Yi-Chun Tsai
Journal:  Int J Mol Sci       Date:  2022-10-03       Impact factor: 6.208

  4 in total

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