An Update on Dipeptidyl Peptidase-IV Inhibiting Peptides.
DPP-IV Inhibitors
Diabetes
Dipeptidyl peptidase-IV
Peptides
Type 2 diabetes mellitus
Journal
Current protein & peptide science
ISSN: 1875-5550
Titre abrégé: Curr Protein Pept Sci
Pays: United Arab Emirates
ID NLM: 100960529
Informations de publication
Date de publication:
03 Jan 2024
03 Jan 2024
Historique:
received:
21
10
2023
revised:
30
11
2023
accepted:
05
12
2023
medline:
4
1
2024
pubmed:
4
1
2024
entrez:
4
1
2024
Statut:
aheadofprint
Résumé
Diabetes is a chronic metabolic disorder. According to the International Diabetes Federation, about 537 million people are living with diabetes. The two types of diabetes are type 1 diabetes mellitus (T1DM) and type 2 diabetes mellitus (T2DM), among which the population affected by T2DM is relatively higher. A major reason for T2DM is that insulin stimulation is hampered due to the inactivation of incretin hormones. Dipeptidyl peptidase-IV (DPP-IV) is a serine protease that is directly involved in the inactivation of incretin hormones, e.g., glucagon-like peptide-1 (GLP-1). Therefore, the inhibition of DPP-IV can be a promising method for managing T2DM, in addition to other enzyme inhibition strategies, such as inhibition of α-amylase and α-glucosidase. Currently, about 12 different gliptin drugs are available in the market that inhibits DPP-IV in a dose-dependent manner. Instead of gliptins, peptides can also be employed as an alternative and promising way to inhibit DPP-IV. Peptide inhibitors of DPP-IV have been identified in various plants and animals. Chemically synthesized peptides have also been experimented with for inhibiting DPP-IV. Most peptides have been analysed by biochemical assays, whereas some in vitro assays have also been reported. Molecular docking analysis is applied to comprehend the mechanism of inhibition. In this review, certain aspects of natural as well as synthetic peptides are described that have been proven to inhibit DPP-IV.
Identifiants
pubmed: 38173201
pii: CPPS-EPUB-136924
doi: 10.2174/0113892037287976231212104607
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
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