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Refinement of long-term toxicity and carcinogenesis studies()

The chance that alternatives will completely replace animals for toxicology research in the foreseeable future is nil. Continual refinement of animal toxicity and carcinogenesis studies, however, can be an effective means of reducing the numbers of animals used and conserving time and resources with...

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Detalles Bibliográficos
Autores principales: Rao, Ghanta N., Huff, James
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Inc. 1990
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126419/
https://www.ncbi.nlm.nih.gov/pubmed/2197145
http://dx.doi.org/10.1016/0272-0590(90)90160-L
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author Rao, Ghanta N.
Huff, James
author_facet Rao, Ghanta N.
Huff, James
author_sort Rao, Ghanta N.
collection PubMed
description The chance that alternatives will completely replace animals for toxicology research in the foreseeable future is nil. Continual refinement of animal toxicity and carcinogenesis studies, however, can be an effective means of reducing the numbers of animals used and conserving time and resources without compromising scientific quality. We must continue to strive to find species and strains that can metabolize chemicals similar to humans, are small enough to be housed in large numbers, and have low prevalence of spontaneous lesions with sufficient life span to express the toxic and carcinogenic potential of chemicals. Adequate care of animals with control of variables such as light, temperature, diet, bedding, diseases, and genetic characters of laboratory animals will decrease the variability. Humane considerations and euthanasia of animals with large masses and other conditions interfering with eating and drinking, major injuries and ulcers related to husbandry and treatment, and diseases indicating pain and suffering will help not only to alleviate further pain and distress but also to facilitate collection of tissues without secondary complications for detection of chemical treatment-related lesions. Limiting the duration of studies to decrease the variability due to ageassociated changes will also refine long-term studies. Other considerations for refinement of carcinogenesis studies include selection of the most sensitive sex of one or more species for evaluation of selected chemicals in a class where toxic and carcinogenic potential of other representative chemicals are known. Genetically engineered animal models with known oncogenes may reduce the duration and increase the sensitivity of carcinogenesis studies with a reduction in the use of animals.
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spelling pubmed-71264192020-04-08 Refinement of long-term toxicity and carcinogenesis studies() Rao, Ghanta N. Huff, James Fundam Appl Toxicol Article The chance that alternatives will completely replace animals for toxicology research in the foreseeable future is nil. Continual refinement of animal toxicity and carcinogenesis studies, however, can be an effective means of reducing the numbers of animals used and conserving time and resources without compromising scientific quality. We must continue to strive to find species and strains that can metabolize chemicals similar to humans, are small enough to be housed in large numbers, and have low prevalence of spontaneous lesions with sufficient life span to express the toxic and carcinogenic potential of chemicals. Adequate care of animals with control of variables such as light, temperature, diet, bedding, diseases, and genetic characters of laboratory animals will decrease the variability. Humane considerations and euthanasia of animals with large masses and other conditions interfering with eating and drinking, major injuries and ulcers related to husbandry and treatment, and diseases indicating pain and suffering will help not only to alleviate further pain and distress but also to facilitate collection of tissues without secondary complications for detection of chemical treatment-related lesions. Limiting the duration of studies to decrease the variability due to ageassociated changes will also refine long-term studies. Other considerations for refinement of carcinogenesis studies include selection of the most sensitive sex of one or more species for evaluation of selected chemicals in a class where toxic and carcinogenic potential of other representative chemicals are known. Genetically engineered animal models with known oncogenes may reduce the duration and increase the sensitivity of carcinogenesis studies with a reduction in the use of animals. Published by Elsevier Inc. 1990-07 2004-09-27 /pmc/articles/PMC7126419/ /pubmed/2197145 http://dx.doi.org/10.1016/0272-0590(90)90160-L Text en Copyright © 1990 Published by Elsevier Inc. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Rao, Ghanta N.
Huff, James
Refinement of long-term toxicity and carcinogenesis studies()
title Refinement of long-term toxicity and carcinogenesis studies()
title_full Refinement of long-term toxicity and carcinogenesis studies()
title_fullStr Refinement of long-term toxicity and carcinogenesis studies()
title_full_unstemmed Refinement of long-term toxicity and carcinogenesis studies()
title_short Refinement of long-term toxicity and carcinogenesis studies()
title_sort refinement of long-term toxicity and carcinogenesis studies()
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126419/
https://www.ncbi.nlm.nih.gov/pubmed/2197145
http://dx.doi.org/10.1016/0272-0590(90)90160-L
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