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二肽基肽酶-4抑制剂除血糖控制外的多效性作用新见解

New Insights into the Pleiotropic Actions of Dipeptidyl Peptidase-4 Inhibitors Beyond Glycaemic Control.

作者信息

Mangoura Safwat A, Ahmed Marwa A, Zaka Andrew Z

机构信息

Department of Pharmacology and Toxicology, Faculty of Pharmacy, Badr University in Cairo (BUC), Badr, Cairo, Egypt.

Department of Medical Pharmacology, Faculty of Medicine, Assiut University, Assiut, Egypt.

出版信息

touchREV Endocrinol. 2024 Oct;20(2):19-29. doi: 10.17925/EE.2024.20.2.5. Epub 2024 Sep 6.

DOI:10.17925/EE.2024.20.2.5
PMID:39526061
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11548370/
Abstract

Dipeptidyl peptidase-4 (DPP-4) is a multifunctional serine ectopeptidase that cleaves and modifies a plethora of substrates, including regulatory peptides, cytokines and chemokines. DPP-4 is implicated in the regulation of immune response, viral entry, cellular adhesion, metastasis and chemotaxis. Regarding its numerous substrates and extensive expression inside the body, multitasking DPP-4 has been assumed to participate in different pathophysiological mechanisms. DPP-4 inhibitors or gliptins are increasingly used for the treatment of type 2 diabetes mellitus. Several reports from experimental and clinical studies have clarified that DPP-4 inhibitors exert many beneficial pleiotropic effects beyond glycaemic control, which are mediated by anti-inflammatory, anti-oxidant, anti-fibrotic and anti-apoptotic actions. The present review will highlight the most recent findings in the literature about these pleiotropic effects and the potential mechanisms underlying these benefits, with a specific focus on the potential effectiveness of DPP-4 inhibitors in coronavirus disease-19 and diabetic kidney disease.

摘要

二肽基肽酶-4(DPP-4)是一种多功能丝氨酸外肽酶,可切割和修饰大量底物,包括调节肽、细胞因子和趋化因子。DPP-4参与免疫反应、病毒进入、细胞黏附、转移和趋化作用的调节。鉴于其众多底物以及在体内的广泛表达,多功能的DPP-4被认为参与了不同的病理生理机制。DPP-4抑制剂或格列汀越来越多地用于治疗2型糖尿病。来自实验和临床研究的几份报告表明,DPP-4抑制剂除了控制血糖外,还发挥许多有益的多效性作用,这些作用由抗炎、抗氧化、抗纤维化和抗凋亡作用介导。本综述将重点介绍文献中关于这些多效性作用的最新发现以及这些益处背后的潜在机制,特别关注DPP-4抑制剂在冠状病毒病-19和糖尿病肾病中的潜在有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f82/11548370/ce48a88f5878/touchendo-20-2-019-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f82/11548370/ce48a88f5878/touchendo-20-2-019-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f82/11548370/ce48a88f5878/touchendo-20-2-019-g001.jpg

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Int J Mol Sci. 2024 Apr 17;25(8):4407. doi: 10.3390/ijms25084407.
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Cyclosporine-induced kidney damage was halted by sitagliptin and hesperidin via increasing Nrf2 and suppressing TNF-α, NF-κB, and Bax.西他列汀和橙皮苷通过增加 Nrf2 和抑制 TNF-α、NF-κB 和 Bax 来阻止环孢素诱导的肾脏损伤。
Sci Rep. 2024 Mar 28;14(1):7434. doi: 10.1038/s41598-024-57300-x.
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Vildagliptin inhibits high fat and fetuin-A mediated DPP-4 expression, intracellular lipid accumulation and improves insulin secretory defects in pancreatic beta cells.
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Biochim Biophys Acta Mol Basis Dis. 2024 Mar;1870(3):167047. doi: 10.1016/j.bbadis.2024.167047. Epub 2024 Jan 29.
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