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Coenzyme Q10 plus Multivitamin Treatment Prevents Cisplatin Ototoxicity in Rats
Cisplatin (Cpt) is known to induce a high level of oxidative stress, resulting in an increase of reactive oxygen species damaging the inner ear and causing hearing loss at high frequencies. Studies on animal models show that antioxidants may lower Cpt-induced ototoxicity. The aim of this study is to...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025172/ https://www.ncbi.nlm.nih.gov/pubmed/27632426 http://dx.doi.org/10.1371/journal.pone.0162106 |
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author | Astolfi, Laura Simoni, Edi Valente, Filippo Ghiselli, Sara Hatzopoulos, Stavros Chicca, Milvia Martini, Alessandro |
author_facet | Astolfi, Laura Simoni, Edi Valente, Filippo Ghiselli, Sara Hatzopoulos, Stavros Chicca, Milvia Martini, Alessandro |
author_sort | Astolfi, Laura |
collection | PubMed |
description | Cisplatin (Cpt) is known to induce a high level of oxidative stress, resulting in an increase of reactive oxygen species damaging the inner ear and causing hearing loss at high frequencies. Studies on animal models show that antioxidants may lower Cpt-induced ototoxicity. The aim of this study is to evaluate the ototoxic effects of two different protocols of Cpt administration in a Sprague-Dawley rat model, and to test in the same model the synergic protective effects of a solution of coenzyme Q10 terclatrate and Acuval 400(®), a multivitamin supplement containing antioxidant agents and minerals (Acu-Qter). The Cpt was administered intraperitoneally in a single dose (14 mg/kg) or in three daily doses (4.6 mg/kg/day) to rats orally treated or untreated with Acu-Qter for 5 days. The auditory function was assessed by measuring auditory brainstem responses from 2 to 32 kHz at day 0 and 5 days after treatment. Similar hearing threshold and body weight alterations were observed in both Cpt administration protocols, but mortality reduced to zero when Cpt was administered in three daily doses. The Acu-Qter treatment was able to prevent and completely neutralize ototoxicity in rats treated with three daily Cpt doses, supporting the synergic protective effects of coenzyme Q terclatrate and Acuval 400(®) against Cpt-induced oxidative stress. The administration protocol involving three Cpt doses is more similar to common human chemotherapy protocols, therefore it appears more useful for long-term preclinical studies on ototoxicity prevention. |
format | Online Article Text |
id | pubmed-5025172 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-50251722016-09-27 Coenzyme Q10 plus Multivitamin Treatment Prevents Cisplatin Ototoxicity in Rats Astolfi, Laura Simoni, Edi Valente, Filippo Ghiselli, Sara Hatzopoulos, Stavros Chicca, Milvia Martini, Alessandro PLoS One Research Article Cisplatin (Cpt) is known to induce a high level of oxidative stress, resulting in an increase of reactive oxygen species damaging the inner ear and causing hearing loss at high frequencies. Studies on animal models show that antioxidants may lower Cpt-induced ototoxicity. The aim of this study is to evaluate the ototoxic effects of two different protocols of Cpt administration in a Sprague-Dawley rat model, and to test in the same model the synergic protective effects of a solution of coenzyme Q10 terclatrate and Acuval 400(®), a multivitamin supplement containing antioxidant agents and minerals (Acu-Qter). The Cpt was administered intraperitoneally in a single dose (14 mg/kg) or in three daily doses (4.6 mg/kg/day) to rats orally treated or untreated with Acu-Qter for 5 days. The auditory function was assessed by measuring auditory brainstem responses from 2 to 32 kHz at day 0 and 5 days after treatment. Similar hearing threshold and body weight alterations were observed in both Cpt administration protocols, but mortality reduced to zero when Cpt was administered in three daily doses. The Acu-Qter treatment was able to prevent and completely neutralize ototoxicity in rats treated with three daily Cpt doses, supporting the synergic protective effects of coenzyme Q terclatrate and Acuval 400(®) against Cpt-induced oxidative stress. The administration protocol involving three Cpt doses is more similar to common human chemotherapy protocols, therefore it appears more useful for long-term preclinical studies on ototoxicity prevention. Public Library of Science 2016-09-15 /pmc/articles/PMC5025172/ /pubmed/27632426 http://dx.doi.org/10.1371/journal.pone.0162106 Text en © 2016 Astolfi et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Astolfi, Laura Simoni, Edi Valente, Filippo Ghiselli, Sara Hatzopoulos, Stavros Chicca, Milvia Martini, Alessandro Coenzyme Q10 plus Multivitamin Treatment Prevents Cisplatin Ototoxicity in Rats |
title | Coenzyme Q10 plus Multivitamin Treatment Prevents Cisplatin Ototoxicity in Rats |
title_full | Coenzyme Q10 plus Multivitamin Treatment Prevents Cisplatin Ototoxicity in Rats |
title_fullStr | Coenzyme Q10 plus Multivitamin Treatment Prevents Cisplatin Ototoxicity in Rats |
title_full_unstemmed | Coenzyme Q10 plus Multivitamin Treatment Prevents Cisplatin Ototoxicity in Rats |
title_short | Coenzyme Q10 plus Multivitamin Treatment Prevents Cisplatin Ototoxicity in Rats |
title_sort | coenzyme q10 plus multivitamin treatment prevents cisplatin ototoxicity in rats |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025172/ https://www.ncbi.nlm.nih.gov/pubmed/27632426 http://dx.doi.org/10.1371/journal.pone.0162106 |
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