Is sitagliptin effective for SARS-CoV-2 infection: false or true prophecy?


Journal

Inflammopharmacology
ISSN: 1568-5608
Titre abrégé: Inflammopharmacology
Pays: Switzerland
ID NLM: 9112626

Informations de publication

Date de publication:
Dec 2022
Historique:
received: 16 08 2022
accepted: 06 09 2022
pubmed: 1 10 2022
medline: 30 11 2022
entrez: 30 9 2022
Statut: ppublish

Résumé

Coronavirus disease 2019 (Covid-19) is caused by severe acute respiratory syndrome type 2 (SARS-CoV-2). Covid-19 is characterized by hyperinflammation, oxidative stress, and multi-organ injury (MOI) such as acute lung injury (ALI) and acute respiratory distress syndrome (ARDS). Covid-19 is mainly presented with respiratory manifestations; however, extra-pulmonary manifestations may also occur. Extra-pulmonary manifestations of Covid-19 are numerous including: neurological, cardiovascular, renal, endocrine, and hematological complications. Notably, a cluster of differentiation 26 (CD26) or dipeptidyl peptidase-4 (DPP-4) emerged as a new receptor for entry of SARS-CoV-2. Therefore, DPP-4 inhibitors like sitagliptin could be effective in treating Covid-19. Hence, we aimed in the present critical review to assess the potential role of sitagliptin in Covid-19. DPP-4 inhibitors are effective against the increased severity of SARS-CoV-2 infections. Moreover, DPP-4 inhibitors inhibit the interaction between DPP-4 and scaffolding proteins which are essential for endosome formation and replication of SARS-CoV-2. Therefore, sitagliptin through attenuation of the inflammatory signaling pathway and augmentation of stromal-derived factor-1 (SDF-1) may decrease the pathogenesis of SARS-CoV-2 infection and could be a possible therapeutic modality in treating Covid-19 patients. In conclusion, the DPP-4 receptor is regarded as a potential receptor for the binding and entry of SARS-CoV-2. Inhibition of these receptors by the DPP-4 inhibitor, sitagliptin, can reduce the pathogenesis of the infection caused by SARS-CoV-2 and their associated activation of the inflammatory signaling pathways.

Identifiants

pubmed: 36180664
doi: 10.1007/s10787-022-01078-9
pii: 10.1007/s10787-022-01078-9
pmc: PMC9524728
doi:

Substances chimiques

Sitagliptin Phosphate TS63EW8X6F
Dipeptidyl-Peptidase IV Inhibitors 0

Types de publication

Review Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2411-2415

Informations de copyright

© 2022. The Author(s).

Références

Arch Immunol Ther Exp (Warsz). 2021 Feb 2;69(1):1
pubmed: 33527308
Diabetes Care. 2021 Apr;44(4):e64-e66
pubmed: 33547204
JAMA. 2007 Jul 11;298(2):194-206
pubmed: 17622601
ASN Neuro. 2021 Jan-Dec;13:17590914211057635
pubmed: 34755562
Life Sci. 2019 Jul 1;228:266-273
pubmed: 31077717
Front Cardiovasc Med. 2021 May 20;8:644095
pubmed: 34124187
Sci Rep. 2022 Jan 7;12(1):180
pubmed: 34996996
Future Sci OA. 2022 Apr 14;8(5):FSO797
pubmed: 35662743
J Endocrinol Invest. 2021 Jul;44(7):1379-1386
pubmed: 33512688
Pharmaceuticals (Basel). 2021 Dec 16;14(12):
pubmed: 34959713
Front Pharmacol. 2022 Apr 26;13:884228
pubmed: 35559257
Mol Cell Biochem. 2022 May;477(5):1381-1392
pubmed: 35147901
Diabetes Metab Res Rev. 2016 May;32(4):391-404
pubmed: 26417956
Int Immunopharmacol. 2022 Mar;104:108516
pubmed: 35032828
Curr Mol Pharmacol. 2022;15(4):683-692
pubmed: 34477540
J Adv Pharm Technol Res. 2020 Jul-Sep;11(3):142-147
pubmed: 33102198
Int J Environ Res Public Health. 2020 May 22;17(10):
pubmed: 32456064
Life Sci. 2021 Mar 15;269:119031
pubmed: 33453244
Naunyn Schmiedebergs Arch Pharmacol. 2021 Oct;394(10):2013-2021
pubmed: 34480616
Diabetes Care. 2020 Dec;43(12):2999-3006
pubmed: 32994187
Mol Biol Rep. 2021 Dec;48(12):8195-8202
pubmed: 34664162
Braz J Microbiol. 2021 Jun;52(2):927-937
pubmed: 33826115
N Engl J Med. 2022 Feb 10;386(6):599-601
pubmed: 35030645
Front Med (Lausanne). 2021 Feb 19;8:644295
pubmed: 33718411
Acta Pharm. 2021 Jun 1;71(2):175-184
pubmed: 33151168
Diabetes Care. 2021 Mar;44(3):e36-e37
pubmed: 33436399

Auteurs

Basil Mohammed Alomair (BM)

Internal Medicine, Endocrinology and Diabetes Department of Medicine, College of Medicine, Aljouf University, Aljouf, Saudi Arabia.

Hayder M Al-Kuraishy (HM)

Department of Pharmacology, Toxicology and Medicine, College of Medicine, Al-Mustansiriyah University, Baghdad, 14132, Iraq.

Ali K Al-Buhadily (AK)

Department of Clinical Pharmacology, Medicine and Therapeutic, Medical Faculty, College of Medicine, Al-Mustansiriyah University, Baghdad, 14132, Iraq.

Ali I Al-Gareeb (AI)

Department of Pharmacology, Toxicology and Medicine, College of Medicine, Al-Mustansiriyah University, Baghdad, 14132, Iraq.

Michel De Waard (M)

Smartox Biotechnology, 6 rue des Platanes, 38120, Saint-Egrève, France.
l'Institut du Thorax, Inserm UMR 1087/CNRS UMR 6291, Nantes, France.
Université de Nice Sophia-Antipolis, LabEx, Ion Channels, Science and Therapeutics, Valbonne, France.

Engy Elekhnawy (E)

Pharmaceutical Microbiology Department, Faculty of Pharmacy, Tanta University, Tanta, 31527, Egypt. engy.ali@pharm.tanta.edu.eg.

Gaber El-Saber Batiha (GE)

Department of Pharmacology and Therapeutics, Faculty of Veterinary Medicine, Damanhour University, Damanhour, 22511, AlBeheira, Egypt. gaberbatiha@gmail.com.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH