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Preventive effect of oral goshajinkigan on chronic oxaliplatin-induced hypoesthesia in rats
Oxaliplatin, a widely used chemotherapeutic agent, induces peripheral neuropathy that manifests itself as two distinct phases: acute cold hyperesthesia and chronic peripheral hypoesthesia/dysesthesia. The latter is a serious dose-limiting side effect that can often lead to withdrawal of treatment. W...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4635352/ https://www.ncbi.nlm.nih.gov/pubmed/26542342 http://dx.doi.org/10.1038/srep16078 |
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author | Kono, Toru Suzuki, Yasuyuki Mizuno, Keita Miyagi, Chika Omiya, Yuji Sekine, Hitomi Mizuhara, Yasuharu Miyano, Kanako Kase, Yoshio Uezono, Yasuhito |
author_facet | Kono, Toru Suzuki, Yasuyuki Mizuno, Keita Miyagi, Chika Omiya, Yuji Sekine, Hitomi Mizuhara, Yasuharu Miyano, Kanako Kase, Yoshio Uezono, Yasuhito |
author_sort | Kono, Toru |
collection | PubMed |
description | Oxaliplatin, a widely used chemotherapeutic agent, induces peripheral neuropathy that manifests itself as two distinct phases: acute cold hyperesthesia and chronic peripheral hypoesthesia/dysesthesia. The latter is a serious dose-limiting side effect that can often lead to withdrawal of treatment. We have developed a rat model expressing both phases and used the model to investigate the action of goshajinkigan (GJG), a traditional Japanese herbal medicine, which was reported to ameliorate oxaliplatin-induced neuropathy in a placebo-controlled double-blind randomized phase II study. In this study, neuropathy was induced by injection of oxaliplatin twice weekly for 8 wks. The maximum level of cold hyperesthesia was observed at 4 wks with heat hypoesthesia developing later. Microscopy studies revealed atrophy of axons of myelinated sciatic nerve fibers in oxaliplatin-treated rats at 8 wks. Co-administration of GJG ameliorated both abnormal sensations as well as histological damage to the sciatic nerve. A pharmacokinetic study revealed numerous neuroprotective components of GJG that are rapidly absorbed into the blood. GJG and some of its components attenuated the generation of oxaliplatin-induced reactive oxygen species, which is a possible mechanism of oxaliplatin-induced neurotoxicity. The present study provides a useful animal model for oxaliplatin-induced neurotoxicity as well as a promising prophylactic agent. |
format | Online Article Text |
id | pubmed-4635352 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46353522015-11-25 Preventive effect of oral goshajinkigan on chronic oxaliplatin-induced hypoesthesia in rats Kono, Toru Suzuki, Yasuyuki Mizuno, Keita Miyagi, Chika Omiya, Yuji Sekine, Hitomi Mizuhara, Yasuharu Miyano, Kanako Kase, Yoshio Uezono, Yasuhito Sci Rep Article Oxaliplatin, a widely used chemotherapeutic agent, induces peripheral neuropathy that manifests itself as two distinct phases: acute cold hyperesthesia and chronic peripheral hypoesthesia/dysesthesia. The latter is a serious dose-limiting side effect that can often lead to withdrawal of treatment. We have developed a rat model expressing both phases and used the model to investigate the action of goshajinkigan (GJG), a traditional Japanese herbal medicine, which was reported to ameliorate oxaliplatin-induced neuropathy in a placebo-controlled double-blind randomized phase II study. In this study, neuropathy was induced by injection of oxaliplatin twice weekly for 8 wks. The maximum level of cold hyperesthesia was observed at 4 wks with heat hypoesthesia developing later. Microscopy studies revealed atrophy of axons of myelinated sciatic nerve fibers in oxaliplatin-treated rats at 8 wks. Co-administration of GJG ameliorated both abnormal sensations as well as histological damage to the sciatic nerve. A pharmacokinetic study revealed numerous neuroprotective components of GJG that are rapidly absorbed into the blood. GJG and some of its components attenuated the generation of oxaliplatin-induced reactive oxygen species, which is a possible mechanism of oxaliplatin-induced neurotoxicity. The present study provides a useful animal model for oxaliplatin-induced neurotoxicity as well as a promising prophylactic agent. Nature Publishing Group 2015-11-06 /pmc/articles/PMC4635352/ /pubmed/26542342 http://dx.doi.org/10.1038/srep16078 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Kono, Toru Suzuki, Yasuyuki Mizuno, Keita Miyagi, Chika Omiya, Yuji Sekine, Hitomi Mizuhara, Yasuharu Miyano, Kanako Kase, Yoshio Uezono, Yasuhito Preventive effect of oral goshajinkigan on chronic oxaliplatin-induced hypoesthesia in rats |
title | Preventive effect of oral goshajinkigan on chronic oxaliplatin-induced hypoesthesia in rats |
title_full | Preventive effect of oral goshajinkigan on chronic oxaliplatin-induced hypoesthesia in rats |
title_fullStr | Preventive effect of oral goshajinkigan on chronic oxaliplatin-induced hypoesthesia in rats |
title_full_unstemmed | Preventive effect of oral goshajinkigan on chronic oxaliplatin-induced hypoesthesia in rats |
title_short | Preventive effect of oral goshajinkigan on chronic oxaliplatin-induced hypoesthesia in rats |
title_sort | preventive effect of oral goshajinkigan on chronic oxaliplatin-induced hypoesthesia in rats |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4635352/ https://www.ncbi.nlm.nih.gov/pubmed/26542342 http://dx.doi.org/10.1038/srep16078 |
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