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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...

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Autores principales: Delay, Eugene R., Socia, Sarah H., Girardin, Jessica L., Jewkes, Benjamin C., King, John H., Delay, Rona J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
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.
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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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