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Single and Repeated Oral Dose Toxicity and Genotoxicity of the Leaves of Butterbur
Butterbur (Petasites japonicus (Siebold & Zucc.) Maxim) leaves are available to consumers in the marketplace, but there is no guarantee that they are safe for human consumption. Previously, we demonstrated that hot water extracts of P. japonicus leaves (KP-1) had anti-inflammatory properties and...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8394925/ https://www.ncbi.nlm.nih.gov/pubmed/34441739 http://dx.doi.org/10.3390/foods10081963 |
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author | Park, Sangsu Lim, Jeongin Lee, Kyung Tae Oh, Myung Sook Jang, Dae Sik |
author_facet | Park, Sangsu Lim, Jeongin Lee, Kyung Tae Oh, Myung Sook Jang, Dae Sik |
author_sort | Park, Sangsu |
collection | PubMed |
description | Butterbur (Petasites japonicus (Siebold & Zucc.) Maxim) leaves are available to consumers in the marketplace, but there is no guarantee that they are safe for human consumption. Previously, we demonstrated that hot water extracts of P. japonicus leaves (KP-1) had anti-inflammatory properties and attenuated memory impairment. However, data regarding KP-1 toxicity are lacking. This study assessed the safety of KP-1 by examining oral and genotoxic effects using in vivo and in vitro tests, respectively. In a single oral dose toxicity and two-week repeated oral dose toxicity study, we observed no toxicologically significant clinical signs or changes in hematology, blood chemistry, and organ weights at any dose during the experiment. Following a thirteen-week repeated oral dose, toxicity, hyperkeratosis, and squamous cell hyperplasia of the limiting ridge in the stomach were observed. The no observable adverse effect level (NOAEL) was found to be 1250 mg/kg/day in male and female rats. However, hyperkeratosis and hyperplasia were not considered to be of toxicological significance when extrapolating the NOAEL to humans because the limiting ridge in the stomach is species-specific to rats. Therefore, in our study, the NOAEL was considered to be 5000 mg/kg/day when the changes in the stomach’s limiting ridge were discounted. Moreover, in vitro bacterial reverse mutations and chromosomal aberrations in Chinese hamster lung (CHL) cells and the in vivo micronucleus in Institute of cancer research (ICR) mice assays showed that KP-1 possessed no mutagenicity. Although additional research is required, these toxicological evaluations suggest that KP-1 could be safe for human consumption. |
format | Online Article Text |
id | pubmed-8394925 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83949252021-08-28 Single and Repeated Oral Dose Toxicity and Genotoxicity of the Leaves of Butterbur Park, Sangsu Lim, Jeongin Lee, Kyung Tae Oh, Myung Sook Jang, Dae Sik Foods Communication Butterbur (Petasites japonicus (Siebold & Zucc.) Maxim) leaves are available to consumers in the marketplace, but there is no guarantee that they are safe for human consumption. Previously, we demonstrated that hot water extracts of P. japonicus leaves (KP-1) had anti-inflammatory properties and attenuated memory impairment. However, data regarding KP-1 toxicity are lacking. This study assessed the safety of KP-1 by examining oral and genotoxic effects using in vivo and in vitro tests, respectively. In a single oral dose toxicity and two-week repeated oral dose toxicity study, we observed no toxicologically significant clinical signs or changes in hematology, blood chemistry, and organ weights at any dose during the experiment. Following a thirteen-week repeated oral dose, toxicity, hyperkeratosis, and squamous cell hyperplasia of the limiting ridge in the stomach were observed. The no observable adverse effect level (NOAEL) was found to be 1250 mg/kg/day in male and female rats. However, hyperkeratosis and hyperplasia were not considered to be of toxicological significance when extrapolating the NOAEL to humans because the limiting ridge in the stomach is species-specific to rats. Therefore, in our study, the NOAEL was considered to be 5000 mg/kg/day when the changes in the stomach’s limiting ridge were discounted. Moreover, in vitro bacterial reverse mutations and chromosomal aberrations in Chinese hamster lung (CHL) cells and the in vivo micronucleus in Institute of cancer research (ICR) mice assays showed that KP-1 possessed no mutagenicity. Although additional research is required, these toxicological evaluations suggest that KP-1 could be safe for human consumption. MDPI 2021-08-23 /pmc/articles/PMC8394925/ /pubmed/34441739 http://dx.doi.org/10.3390/foods10081963 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Park, Sangsu Lim, Jeongin Lee, Kyung Tae Oh, Myung Sook Jang, Dae Sik Single and Repeated Oral Dose Toxicity and Genotoxicity of the Leaves of Butterbur |
title | Single and Repeated Oral Dose Toxicity and Genotoxicity of the Leaves of Butterbur |
title_full | Single and Repeated Oral Dose Toxicity and Genotoxicity of the Leaves of Butterbur |
title_fullStr | Single and Repeated Oral Dose Toxicity and Genotoxicity of the Leaves of Butterbur |
title_full_unstemmed | Single and Repeated Oral Dose Toxicity and Genotoxicity of the Leaves of Butterbur |
title_short | Single and Repeated Oral Dose Toxicity and Genotoxicity of the Leaves of Butterbur |
title_sort | single and repeated oral dose toxicity and genotoxicity of the leaves of butterbur |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8394925/ https://www.ncbi.nlm.nih.gov/pubmed/34441739 http://dx.doi.org/10.3390/foods10081963 |
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