» Articles » PMID: 34830194

Incretins in the Therapy of Diabetic Kidney Disease

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2021 Nov 27
PMID 34830194
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

Diabetic kidney disease is a microvascular complication that occurs in patients with diabetes. It is strongly associated with increased risk of kidney replacement therapy and all-cause mortality. Incretins are peptide hormones derived from the gastrointestinal tract, that besides causing enhancement of insulin secretion after oral glucose intake, participate in many other metabolic processes. Antidiabetic drug classes, such as dipeptidyl peptidase 4 inhibitors and glucagon-like peptide receptor agonists, which way of action is based on incretins facility, not only show glucose-lowering properties but also have nephroprotective functions. The aim of this article is to present the latest information about incretin-based therapy and its influence on diabetic kidney disease appearance and progression, point its potential mechanisms of kidney protection and focus on future therapeutic possibilities bound with these two antidiabetic drug classes.

Citing Articles

A Specific Collagen Hydrolysate Improves Postprandial Glucose Tolerance in Normoglycemic and Prediabetic Mice and in a First Proof of Concept Study in Healthy, Normoglycemic and Prediabetic Humans.

Grasset E, Briand F, Virgilio N, Schon C, Wilhelm M, Cudennec B Food Sci Nutr. 2024; 12(11):9607-9620.

PMID: 39619994 PMC: 11606891. DOI: 10.1002/fsn3.4538.


Incretin-based therapy: a new horizon in diabetes management.

Zarei M, Sahebi Vaighan N, Farjoo M, Talebi S, Zarei M J Diabetes Metab Disord. 2024; 23(2):1665-1686.

PMID: 39610543 PMC: 11599551. DOI: 10.1007/s40200-024-01479-3.


Molecular Characterization and Functional Analysis of the Dipeptidyl Peptidase IV from Venom of the Ectoparasitoid .

Wu C, Yang C, Wang Y, Wang J, Zhu J Toxins (Basel). 2023; 15(5).

PMID: 37235347 PMC: 10222045. DOI: 10.3390/toxins15050311.


Sitagliptin Mitigates Diabetic Nephropathy in a Rat Model of Streptozotocin-Induced Type 2 Diabetes: Possible Role of PTP1B/JAK-STAT Pathway.

Al-Qabbaa S, Qaboli S, Alshammari T, Alamin M, Alrajeh H, Almuthnabi L Int J Mol Sci. 2023; 24(7).

PMID: 37047505 PMC: 10095069. DOI: 10.3390/ijms24076532.


Links between Metabolic Syndrome and Hypertension: The Relationship with the Current Antidiabetic Drugs.

Stanciu S, Rusu E, Miricescu D, Radu A, Axinia B, Vrabie A Metabolites. 2023; 13(1).

PMID: 36677012 PMC: 9863091. DOI: 10.3390/metabo13010087.


References
1.
Yang H, Li H, Wang Z, Shi Y, Jiang G, Zeng F . Exendin-4 ameliorates renal ischemia-reperfusion injury in the rat. J Surg Res. 2013; 185(2):825-32. DOI: 10.1016/j.jss.2013.06.042. View

2.
Barros R, Gabbi C, Morani A, Warner M, Gustafsson J . Participation of ERalpha and ERbeta in glucose homeostasis in skeletal muscle and white adipose tissue. Am J Physiol Endocrinol Metab. 2009; 297(1):E124-33. DOI: 10.1152/ajpendo.00189.2009. View

3.
Twarog C, Fattah S, Heade J, Maher S, Fattal E, Brayden D . Intestinal Permeation Enhancers for Oral Delivery of Macromolecules: A Comparison between Salcaprozate Sodium (SNAC) and Sodium Caprate (C). Pharmaceutics. 2019; 11(2). PMC: 6410172. DOI: 10.3390/pharmaceutics11020078. View

4.
Tonneijck L, Muskiet M, Smits M, Hoekstra T, Kramer M, Danser A . Postprandial renal haemodynamic effect of lixisenatide vs once-daily insulin-glulisine in patients with type 2 diabetes on insulin-glargine: An 8-week, randomised, open-label trial. Diabetes Obes Metab. 2017; 19(12):1669-1680. DOI: 10.1111/dom.12985. View

5.
Yaribeygi H, Sathyapalan T, Sahebkar A . Molecular mechanisms by which GLP-1 RA and DPP-4i induce insulin sensitivity. Life Sci. 2019; 234:116776. DOI: 10.1016/j.lfs.2019.116776. View