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Oral Administration of Caffeine Exacerbates Cisplatin-Induced Hearing Loss

Adenosine A(1) receptors (A(1)AR) are well characterized for their role in cytoprotection. Previous studies have demonstrated the presence of these receptors in the cochlea where their activation were shown to suppress cisplatin-induced inflammatory response and the resulting ototoxicity. Inhibition...

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Autores principales: Sheth, Sandeep, Sheehan, Kelly, Dhukhwa, Asmita, Al Aameri, Raheem F. H., Mamillapalli, Chaitanya, Mukherjea, Debashree, Rybak, Leonard P., Ramkumar, Vickram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6606569/
https://www.ncbi.nlm.nih.gov/pubmed/31267026
http://dx.doi.org/10.1038/s41598-019-45964-9
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author Sheth, Sandeep
Sheehan, Kelly
Dhukhwa, Asmita
Al Aameri, Raheem F. H.
Mamillapalli, Chaitanya
Mukherjea, Debashree
Rybak, Leonard P.
Ramkumar, Vickram
author_facet Sheth, Sandeep
Sheehan, Kelly
Dhukhwa, Asmita
Al Aameri, Raheem F. H.
Mamillapalli, Chaitanya
Mukherjea, Debashree
Rybak, Leonard P.
Ramkumar, Vickram
author_sort Sheth, Sandeep
collection PubMed
description Adenosine A(1) receptors (A(1)AR) are well characterized for their role in cytoprotection. Previous studies have demonstrated the presence of these receptors in the cochlea where their activation were shown to suppress cisplatin-induced inflammatory response and the resulting ototoxicity. Inhibition of A(1)AR by caffeine, a widely consumed psychoactive substance, could antagonize the endogenous protective role of these receptors in cochlea and potentiate cisplatin-induced hearing loss. This hypothesis was tested in a rat model of cisplatin ototoxicity following oral administration of caffeine. We report here that single-dose administration of caffeine exacerbates cisplatin-induced hearing loss without increasing the damage to outer hair cells (OHCs), but increased synaptopathy and inflammation in the cochlea. These effects of caffeine were mediated by its blockade of A(1)AR, as co-administration of R-PIA, an A(1)AR agonist, reversed the detrimental actions of caffeine and cisplatin on hearing loss. Multiple doses of caffeine exacerbated cisplatin ototoxicity which was associated with damage to OHCs and cochlear synaptopathy. These findings highlight a possible drug-drug interaction between caffeine and cisplatin for ototoxicity and suggest that caffeine consumption should be cautioned in cancer patients treated with a chemotherapeutic regimen containing cisplatin.
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spelling pubmed-66065692019-07-14 Oral Administration of Caffeine Exacerbates Cisplatin-Induced Hearing Loss Sheth, Sandeep Sheehan, Kelly Dhukhwa, Asmita Al Aameri, Raheem F. H. Mamillapalli, Chaitanya Mukherjea, Debashree Rybak, Leonard P. Ramkumar, Vickram Sci Rep Article Adenosine A(1) receptors (A(1)AR) are well characterized for their role in cytoprotection. Previous studies have demonstrated the presence of these receptors in the cochlea where their activation were shown to suppress cisplatin-induced inflammatory response and the resulting ototoxicity. Inhibition of A(1)AR by caffeine, a widely consumed psychoactive substance, could antagonize the endogenous protective role of these receptors in cochlea and potentiate cisplatin-induced hearing loss. This hypothesis was tested in a rat model of cisplatin ototoxicity following oral administration of caffeine. We report here that single-dose administration of caffeine exacerbates cisplatin-induced hearing loss without increasing the damage to outer hair cells (OHCs), but increased synaptopathy and inflammation in the cochlea. These effects of caffeine were mediated by its blockade of A(1)AR, as co-administration of R-PIA, an A(1)AR agonist, reversed the detrimental actions of caffeine and cisplatin on hearing loss. Multiple doses of caffeine exacerbated cisplatin ototoxicity which was associated with damage to OHCs and cochlear synaptopathy. These findings highlight a possible drug-drug interaction between caffeine and cisplatin for ototoxicity and suggest that caffeine consumption should be cautioned in cancer patients treated with a chemotherapeutic regimen containing cisplatin. Nature Publishing Group UK 2019-07-02 /pmc/articles/PMC6606569/ /pubmed/31267026 http://dx.doi.org/10.1038/s41598-019-45964-9 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Sheth, Sandeep
Sheehan, Kelly
Dhukhwa, Asmita
Al Aameri, Raheem F. H.
Mamillapalli, Chaitanya
Mukherjea, Debashree
Rybak, Leonard P.
Ramkumar, Vickram
Oral Administration of Caffeine Exacerbates Cisplatin-Induced Hearing Loss
title Oral Administration of Caffeine Exacerbates Cisplatin-Induced Hearing Loss
title_full Oral Administration of Caffeine Exacerbates Cisplatin-Induced Hearing Loss
title_fullStr Oral Administration of Caffeine Exacerbates Cisplatin-Induced Hearing Loss
title_full_unstemmed Oral Administration of Caffeine Exacerbates Cisplatin-Induced Hearing Loss
title_short Oral Administration of Caffeine Exacerbates Cisplatin-Induced Hearing Loss
title_sort oral administration of caffeine exacerbates cisplatin-induced hearing loss
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6606569/
https://www.ncbi.nlm.nih.gov/pubmed/31267026
http://dx.doi.org/10.1038/s41598-019-45964-9
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