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Drug-induced mitochondrial toxicity: Risks of developing glucose handling impairments

Mitochondrial impairment has been associated with the development of insulin resistance, the hallmark of type 2 diabetes mellitus (T2DM). However, the relationship between mitochondrial impairment and insulin resistance is not fully elucidated due to insufficient evidence to support the hypothesis....

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Autores principales: Kuretu, Auxiliare, Arineitwe, Charles, Mothibe, Mamosheledi, Ngubane, Phikelelani, Khathi, Andile, Sibiya, Ntethelelo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9969099/
https://www.ncbi.nlm.nih.gov/pubmed/36860368
http://dx.doi.org/10.3389/fendo.2023.1123928
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author Kuretu, Auxiliare
Arineitwe, Charles
Mothibe, Mamosheledi
Ngubane, Phikelelani
Khathi, Andile
Sibiya, Ntethelelo
author_facet Kuretu, Auxiliare
Arineitwe, Charles
Mothibe, Mamosheledi
Ngubane, Phikelelani
Khathi, Andile
Sibiya, Ntethelelo
author_sort Kuretu, Auxiliare
collection PubMed
description Mitochondrial impairment has been associated with the development of insulin resistance, the hallmark of type 2 diabetes mellitus (T2DM). However, the relationship between mitochondrial impairment and insulin resistance is not fully elucidated due to insufficient evidence to support the hypothesis. Insulin resistance and insulin deficiency are both characterised by excessive production of reactive oxygen species and mitochondrial coupling. Compelling evidence states that improving the function of the mitochondria may provide a positive therapeutic tool for improving insulin sensitivity. There has been a rapid increase in reports of the toxic effects of drugs and pollutants on the mitochondria in recent decades, interestingly correlating with an increase in insulin resistance prevalence. A variety of drug classes have been reported to potentially induce toxicity in the mitochondria leading to skeletal muscle, liver, central nervous system, and kidney injury. With the increase in diabetes prevalence and mitochondrial toxicity, it is therefore imperative to understand how mitochondrial toxicological agents can potentially compromise insulin sensitivity. This review article aims to explore and summarise the correlation between potential mitochondrial dysfunction caused by selected pharmacological agents and its effect on insulin signalling and glucose handling. Additionally, this review highlights the necessity for further studies aimed to understand drug-induced mitochondrial toxicity and the development of insulin resistance.
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spelling pubmed-99690992023-02-28 Drug-induced mitochondrial toxicity: Risks of developing glucose handling impairments Kuretu, Auxiliare Arineitwe, Charles Mothibe, Mamosheledi Ngubane, Phikelelani Khathi, Andile Sibiya, Ntethelelo Front Endocrinol (Lausanne) Endocrinology Mitochondrial impairment has been associated with the development of insulin resistance, the hallmark of type 2 diabetes mellitus (T2DM). However, the relationship between mitochondrial impairment and insulin resistance is not fully elucidated due to insufficient evidence to support the hypothesis. Insulin resistance and insulin deficiency are both characterised by excessive production of reactive oxygen species and mitochondrial coupling. Compelling evidence states that improving the function of the mitochondria may provide a positive therapeutic tool for improving insulin sensitivity. There has been a rapid increase in reports of the toxic effects of drugs and pollutants on the mitochondria in recent decades, interestingly correlating with an increase in insulin resistance prevalence. A variety of drug classes have been reported to potentially induce toxicity in the mitochondria leading to skeletal muscle, liver, central nervous system, and kidney injury. With the increase in diabetes prevalence and mitochondrial toxicity, it is therefore imperative to understand how mitochondrial toxicological agents can potentially compromise insulin sensitivity. This review article aims to explore and summarise the correlation between potential mitochondrial dysfunction caused by selected pharmacological agents and its effect on insulin signalling and glucose handling. Additionally, this review highlights the necessity for further studies aimed to understand drug-induced mitochondrial toxicity and the development of insulin resistance. Frontiers Media S.A. 2023-02-13 /pmc/articles/PMC9969099/ /pubmed/36860368 http://dx.doi.org/10.3389/fendo.2023.1123928 Text en Copyright © 2023 Kuretu, Arineitwe, Mothibe, Ngubane, Khathi and Sibiya 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
Kuretu, Auxiliare
Arineitwe, Charles
Mothibe, Mamosheledi
Ngubane, Phikelelani
Khathi, Andile
Sibiya, Ntethelelo
Drug-induced mitochondrial toxicity: Risks of developing glucose handling impairments
title Drug-induced mitochondrial toxicity: Risks of developing glucose handling impairments
title_full Drug-induced mitochondrial toxicity: Risks of developing glucose handling impairments
title_fullStr Drug-induced mitochondrial toxicity: Risks of developing glucose handling impairments
title_full_unstemmed Drug-induced mitochondrial toxicity: Risks of developing glucose handling impairments
title_short Drug-induced mitochondrial toxicity: Risks of developing glucose handling impairments
title_sort drug-induced mitochondrial toxicity: risks of developing glucose handling impairments
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9969099/
https://www.ncbi.nlm.nih.gov/pubmed/36860368
http://dx.doi.org/10.3389/fendo.2023.1123928
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