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Interaction of Severe Acute Respiratory Syndrome Coronavirus 2 and Diabetes

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is causing a worldwide epidemic. It spreads very fast and hits people of all ages, especially patients with underlying diseases such as diabetes. In this review, we focus on the influences of diabetes on the outcome of SARS-CoV-2 infection...

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Autores principales: Shao, Shiying, Yang, Qin, Pan, Ruping, Yu, Xuefeng, Chen, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8527093/
https://www.ncbi.nlm.nih.gov/pubmed/34690930
http://dx.doi.org/10.3389/fendo.2021.731974
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author Shao, Shiying
Yang, Qin
Pan, Ruping
Yu, Xuefeng
Chen, Yong
author_facet Shao, Shiying
Yang, Qin
Pan, Ruping
Yu, Xuefeng
Chen, Yong
author_sort Shao, Shiying
collection PubMed
description Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is causing a worldwide epidemic. It spreads very fast and hits people of all ages, especially patients with underlying diseases such as diabetes. In this review, we focus on the influences of diabetes on the outcome of SARS-CoV-2 infection and the involved mechanisms including lung dysfunction, immune disorder, abnormal expression of angiotensin-converting enzyme 2 (ACE2), overactivation of mechanistic target of rapamycin (mTOR) signaling pathway, and increased furin level. On the other hand, SARS-CoV-2 may trigger the development of diabetes. It causes the damage of pancreatic β cells, which is probably mediated by ACE2 protein in the islets. Furthermore, SARS-CoV-2 may aggravate insulin resistance through attacking other metabolic organs. Of note, certain anti-diabetic drugs (OADs), such as peroxisome proliferator-activated receptor γ (PPARγ) activator and glucagon-like peptide 1 receptor (GLP-1R) agonist, have been shown to upregulate ACE2 in animal models, which may increase the risk of SARS-CoV-2 infection. However, Metformin, as a first-line medicine for the treatment of type 2 diabetes mellitus (T2DM), may be a potential drug benefiting diabetic patients with SARS-CoV-2 infection, probably via a suppression of mTOR signaling together with its anti-inflammatory and anti-fibrosis function in lung. Remarkably, another kind of OADs, dipeptidyl Peptidase 4 (DPP4) inhibitor, may also exert beneficial effects in this respect, probably via a prevention of SARS-CoV-2 binding to cells. Thus, it is of significant to identify appropriate OADs for the treatment of diabetes in the context of SARS-CoV-2 infections.
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spelling pubmed-85270932021-10-21 Interaction of Severe Acute Respiratory Syndrome Coronavirus 2 and Diabetes Shao, Shiying Yang, Qin Pan, Ruping Yu, Xuefeng Chen, Yong Front Endocrinol (Lausanne) Endocrinology Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is causing a worldwide epidemic. It spreads very fast and hits people of all ages, especially patients with underlying diseases such as diabetes. In this review, we focus on the influences of diabetes on the outcome of SARS-CoV-2 infection and the involved mechanisms including lung dysfunction, immune disorder, abnormal expression of angiotensin-converting enzyme 2 (ACE2), overactivation of mechanistic target of rapamycin (mTOR) signaling pathway, and increased furin level. On the other hand, SARS-CoV-2 may trigger the development of diabetes. It causes the damage of pancreatic β cells, which is probably mediated by ACE2 protein in the islets. Furthermore, SARS-CoV-2 may aggravate insulin resistance through attacking other metabolic organs. Of note, certain anti-diabetic drugs (OADs), such as peroxisome proliferator-activated receptor γ (PPARγ) activator and glucagon-like peptide 1 receptor (GLP-1R) agonist, have been shown to upregulate ACE2 in animal models, which may increase the risk of SARS-CoV-2 infection. However, Metformin, as a first-line medicine for the treatment of type 2 diabetes mellitus (T2DM), may be a potential drug benefiting diabetic patients with SARS-CoV-2 infection, probably via a suppression of mTOR signaling together with its anti-inflammatory and anti-fibrosis function in lung. Remarkably, another kind of OADs, dipeptidyl Peptidase 4 (DPP4) inhibitor, may also exert beneficial effects in this respect, probably via a prevention of SARS-CoV-2 binding to cells. Thus, it is of significant to identify appropriate OADs for the treatment of diabetes in the context of SARS-CoV-2 infections. Frontiers Media S.A. 2021-10-06 /pmc/articles/PMC8527093/ /pubmed/34690930 http://dx.doi.org/10.3389/fendo.2021.731974 Text en Copyright © 2021 Shao, Yang, Pan, Yu and Chen https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Shao, Shiying
Yang, Qin
Pan, Ruping
Yu, Xuefeng
Chen, Yong
Interaction of Severe Acute Respiratory Syndrome Coronavirus 2 and Diabetes
title Interaction of Severe Acute Respiratory Syndrome Coronavirus 2 and Diabetes
title_full Interaction of Severe Acute Respiratory Syndrome Coronavirus 2 and Diabetes
title_fullStr Interaction of Severe Acute Respiratory Syndrome Coronavirus 2 and Diabetes
title_full_unstemmed Interaction of Severe Acute Respiratory Syndrome Coronavirus 2 and Diabetes
title_short Interaction of Severe Acute Respiratory Syndrome Coronavirus 2 and Diabetes
title_sort interaction of severe acute respiratory syndrome coronavirus 2 and diabetes
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8527093/
https://www.ncbi.nlm.nih.gov/pubmed/34690930
http://dx.doi.org/10.3389/fendo.2021.731974
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