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Cyclophosphamide and the taste system: Effects of dose fractionation and amifostine on taste cell renewal
Chemotherapy often causes side effects that include disturbances in taste functions. Cyclophosphamide (CYP) is a chemotherapy drug that, after a single dose, elevates murine taste thresholds at times related to drug-induced losses of taste sensory cells and disruptions of proliferating cells that re...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6448888/ https://www.ncbi.nlm.nih.gov/pubmed/30947285 http://dx.doi.org/10.1371/journal.pone.0214890 |
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author | Delay, Eugene R. Socia, Sarah H. Girardin, Jessica L. Jewkes, Benjamin C. King, John H. Delay, Rona J. |
author_facet | Delay, Eugene R. Socia, Sarah H. Girardin, Jessica L. Jewkes, Benjamin C. King, John H. Delay, Rona J. |
author_sort | Delay, Eugene R. |
collection | PubMed |
description | Chemotherapy often causes side effects that include disturbances in taste functions. Cyclophosphamide (CYP) is a chemotherapy drug that, after a single dose, elevates murine taste thresholds at times related to drug-induced losses of taste sensory cells and disruptions of proliferating cells that renew taste sensory cells. Pretreatment with amifostine can protect the taste system from many of these effects. This study compared the effects of a single dose (75 mg/kg) of CYP with effects generated by fractionated dosing of CYP (5 doses of 15 mg/kg), a dosing approach often used during chemotherapy, on the taste system of mice using immunohistochemistry. Dose fractionation prolonged the suppressive effects of CYP on cell proliferation responsible for renewal of taste sensory cells. Fractionation also reduced the total number of cells and the proportion of Type II cells within taste buds. The post-injection time of these losses coincided with the life span of Type I and II taste cells combined with lack of replacement cells. Fractionated dosing also decreased Type III cells more than a single dose, but loss of these cells may be due to factors related to the general health and/or cell renewal of taste buds rather than the life span of Type III cells. In general, pretreatment with amifostine appeared to protect taste cell renewal and the population of cells within taste buds from the cytotoxic effects of CYP with few observable adverse effects due to repeated administration. These findings may have important implications for patients undergoing chemotherapy. |
format | Online Article Text |
id | pubmed-6448888 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-64488882019-04-19 Cyclophosphamide and the taste system: Effects of dose fractionation and amifostine on taste cell renewal Delay, Eugene R. Socia, Sarah H. Girardin, Jessica L. Jewkes, Benjamin C. King, John H. Delay, Rona J. PLoS One Research Article Chemotherapy often causes side effects that include disturbances in taste functions. Cyclophosphamide (CYP) is a chemotherapy drug that, after a single dose, elevates murine taste thresholds at times related to drug-induced losses of taste sensory cells and disruptions of proliferating cells that renew taste sensory cells. Pretreatment with amifostine can protect the taste system from many of these effects. This study compared the effects of a single dose (75 mg/kg) of CYP with effects generated by fractionated dosing of CYP (5 doses of 15 mg/kg), a dosing approach often used during chemotherapy, on the taste system of mice using immunohistochemistry. Dose fractionation prolonged the suppressive effects of CYP on cell proliferation responsible for renewal of taste sensory cells. Fractionation also reduced the total number of cells and the proportion of Type II cells within taste buds. The post-injection time of these losses coincided with the life span of Type I and II taste cells combined with lack of replacement cells. Fractionated dosing also decreased Type III cells more than a single dose, but loss of these cells may be due to factors related to the general health and/or cell renewal of taste buds rather than the life span of Type III cells. In general, pretreatment with amifostine appeared to protect taste cell renewal and the population of cells within taste buds from the cytotoxic effects of CYP with few observable adverse effects due to repeated administration. These findings may have important implications for patients undergoing chemotherapy. Public Library of Science 2019-04-04 /pmc/articles/PMC6448888/ /pubmed/30947285 http://dx.doi.org/10.1371/journal.pone.0214890 Text en © 2019 Delay 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 Delay, Eugene R. Socia, Sarah H. Girardin, Jessica L. Jewkes, Benjamin C. King, John H. Delay, Rona J. Cyclophosphamide and the taste system: Effects of dose fractionation and amifostine on taste cell renewal |
title | Cyclophosphamide and the taste system: Effects of dose fractionation and amifostine on taste cell renewal |
title_full | Cyclophosphamide and the taste system: Effects of dose fractionation and amifostine on taste cell renewal |
title_fullStr | Cyclophosphamide and the taste system: Effects of dose fractionation and amifostine on taste cell renewal |
title_full_unstemmed | Cyclophosphamide and the taste system: Effects of dose fractionation and amifostine on taste cell renewal |
title_short | Cyclophosphamide and the taste system: Effects of dose fractionation and amifostine on taste cell renewal |
title_sort | cyclophosphamide and the taste system: effects of dose fractionation and amifostine on taste cell renewal |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6448888/ https://www.ncbi.nlm.nih.gov/pubmed/30947285 http://dx.doi.org/10.1371/journal.pone.0214890 |
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