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Dehydropyrrolizidine Alkaloid Toxicity, Cytotoxicity, and Carcinogenicity
Dehydropyrrolizidine alkaloid (DHPA)-producing plants have a worldwide distribution amongst flowering plants and commonly cause poisoning of livestock, wildlife, and humans. Previous work has produced considerable understanding of DHPA metabolism, toxicity, species susceptibility, conditions, and ro...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5198550/ https://www.ncbi.nlm.nih.gov/pubmed/27916846 http://dx.doi.org/10.3390/toxins8120356 |
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author | Stegelmeier, Bryan L. Colegate, Steven M. Brown, Ammon W. |
author_facet | Stegelmeier, Bryan L. Colegate, Steven M. Brown, Ammon W. |
author_sort | Stegelmeier, Bryan L. |
collection | PubMed |
description | Dehydropyrrolizidine alkaloid (DHPA)-producing plants have a worldwide distribution amongst flowering plants and commonly cause poisoning of livestock, wildlife, and humans. Previous work has produced considerable understanding of DHPA metabolism, toxicity, species susceptibility, conditions, and routes of exposure, and pathogenesis of acute poisoning. Intoxication is generally caused by contaminated grains, feed, flour, and breads that result in acute, high-dose, short-duration poisoning. Acute poisoning produces hepatic necrosis that is usually confirmed histologically, epidemiologically, and chemically. Less is known about chronic poisoning that may result when plant populations are sporadic, used as tisanes or herbal preparations, or when DHPAs contaminate milk, honey, pollen, or other animal-derived products. Such subclinical exposures may contribute to the development of chronic disease in humans or may be cumulative and probably slowly progress until liver failure. Recent work using rodent models suggest increased neoplastic incidence even with very low DHPA doses of short durations. These concerns have moved some governments to prohibit or limit human exposure to DHPAs. The purpose of this review is to summarize some recent DHPA research, including in vitro and in vivo DHPA toxicity and carcinogenicity reports, and the implications of these findings with respect to diagnosis and prognosis for human and animal health. |
format | Online Article Text |
id | pubmed-5198550 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-51985502017-01-03 Dehydropyrrolizidine Alkaloid Toxicity, Cytotoxicity, and Carcinogenicity Stegelmeier, Bryan L. Colegate, Steven M. Brown, Ammon W. Toxins (Basel) Review Dehydropyrrolizidine alkaloid (DHPA)-producing plants have a worldwide distribution amongst flowering plants and commonly cause poisoning of livestock, wildlife, and humans. Previous work has produced considerable understanding of DHPA metabolism, toxicity, species susceptibility, conditions, and routes of exposure, and pathogenesis of acute poisoning. Intoxication is generally caused by contaminated grains, feed, flour, and breads that result in acute, high-dose, short-duration poisoning. Acute poisoning produces hepatic necrosis that is usually confirmed histologically, epidemiologically, and chemically. Less is known about chronic poisoning that may result when plant populations are sporadic, used as tisanes or herbal preparations, or when DHPAs contaminate milk, honey, pollen, or other animal-derived products. Such subclinical exposures may contribute to the development of chronic disease in humans or may be cumulative and probably slowly progress until liver failure. Recent work using rodent models suggest increased neoplastic incidence even with very low DHPA doses of short durations. These concerns have moved some governments to prohibit or limit human exposure to DHPAs. The purpose of this review is to summarize some recent DHPA research, including in vitro and in vivo DHPA toxicity and carcinogenicity reports, and the implications of these findings with respect to diagnosis and prognosis for human and animal health. MDPI 2016-11-29 /pmc/articles/PMC5198550/ /pubmed/27916846 http://dx.doi.org/10.3390/toxins8120356 Text en © 2016 by the authors; 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Stegelmeier, Bryan L. Colegate, Steven M. Brown, Ammon W. Dehydropyrrolizidine Alkaloid Toxicity, Cytotoxicity, and Carcinogenicity |
title | Dehydropyrrolizidine Alkaloid Toxicity, Cytotoxicity, and Carcinogenicity |
title_full | Dehydropyrrolizidine Alkaloid Toxicity, Cytotoxicity, and Carcinogenicity |
title_fullStr | Dehydropyrrolizidine Alkaloid Toxicity, Cytotoxicity, and Carcinogenicity |
title_full_unstemmed | Dehydropyrrolizidine Alkaloid Toxicity, Cytotoxicity, and Carcinogenicity |
title_short | Dehydropyrrolizidine Alkaloid Toxicity, Cytotoxicity, and Carcinogenicity |
title_sort | dehydropyrrolizidine alkaloid toxicity, cytotoxicity, and carcinogenicity |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5198550/ https://www.ncbi.nlm.nih.gov/pubmed/27916846 http://dx.doi.org/10.3390/toxins8120356 |
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