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Zoopharmacognosy in Diseased Laboratory Mice: Conflicting Evidence

Zoopharmacognosy denotes a constellation of learned ingestive responses that promote healing and survival of infected or poisoned animals. A similar self-medication phenomenon was reported in diseased laboratory rodents. In particular, a series of studies revealed that autoimmune MRL/lpr mice readil...

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Autores principales: Kapadia, Minesh, Zhao, Hui, Ma, Donglai, Hatkar, Rupal, Marchese, Monica, Sakic, Boris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4067353/
https://www.ncbi.nlm.nih.gov/pubmed/24956477
http://dx.doi.org/10.1371/journal.pone.0100684
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author Kapadia, Minesh
Zhao, Hui
Ma, Donglai
Hatkar, Rupal
Marchese, Monica
Sakic, Boris
author_facet Kapadia, Minesh
Zhao, Hui
Ma, Donglai
Hatkar, Rupal
Marchese, Monica
Sakic, Boris
author_sort Kapadia, Minesh
collection PubMed
description Zoopharmacognosy denotes a constellation of learned ingestive responses that promote healing and survival of infected or poisoned animals. A similar self-medication phenomenon was reported in diseased laboratory rodents. In particular, a series of studies revealed that autoimmune MRL/lpr mice readily consume solutions paired or laced with cyclophosphamide (CY), an immunosuppressive drug that prevents inflammatory damage to internal organs. However, due to design limitations, it could not be elucidated whether such a response reflects the learned therapeutic effect of CY, or a deficit in sensory input. We presently assess the behavioural effects of prolonged consumption of CY-laced, 16% sucrose solution in a continuous choice paradigm, with tap water available ad lib. Contrary to overall expectation, MRL/lpr mice did not increase their intake of CY with disease progression. Moreover, they ingested lower doses of CY and preferred less CY-laced sucrose solution than age-matched controls. The results obtained could not confirm zoopharmacognosy in diseased MRL/lpr mice, likely due to impaired responsiveness to palatable stimulation, or attenuated survival mechanisms after prolonged inbreeding in captivity. However, by revealing the effectiveness of unrestricted drinking of drug-laced sucrose solution on behavior and immunity, the current study supports broader use of such an administration route in behavioural studies sensitive to external stressors.
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spelling pubmed-40673532014-06-25 Zoopharmacognosy in Diseased Laboratory Mice: Conflicting Evidence Kapadia, Minesh Zhao, Hui Ma, Donglai Hatkar, Rupal Marchese, Monica Sakic, Boris PLoS One Research Article Zoopharmacognosy denotes a constellation of learned ingestive responses that promote healing and survival of infected or poisoned animals. A similar self-medication phenomenon was reported in diseased laboratory rodents. In particular, a series of studies revealed that autoimmune MRL/lpr mice readily consume solutions paired or laced with cyclophosphamide (CY), an immunosuppressive drug that prevents inflammatory damage to internal organs. However, due to design limitations, it could not be elucidated whether such a response reflects the learned therapeutic effect of CY, or a deficit in sensory input. We presently assess the behavioural effects of prolonged consumption of CY-laced, 16% sucrose solution in a continuous choice paradigm, with tap water available ad lib. Contrary to overall expectation, MRL/lpr mice did not increase their intake of CY with disease progression. Moreover, they ingested lower doses of CY and preferred less CY-laced sucrose solution than age-matched controls. The results obtained could not confirm zoopharmacognosy in diseased MRL/lpr mice, likely due to impaired responsiveness to palatable stimulation, or attenuated survival mechanisms after prolonged inbreeding in captivity. However, by revealing the effectiveness of unrestricted drinking of drug-laced sucrose solution on behavior and immunity, the current study supports broader use of such an administration route in behavioural studies sensitive to external stressors. Public Library of Science 2014-06-23 /pmc/articles/PMC4067353/ /pubmed/24956477 http://dx.doi.org/10.1371/journal.pone.0100684 Text en © 2014 Kapadia 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Kapadia, Minesh
Zhao, Hui
Ma, Donglai
Hatkar, Rupal
Marchese, Monica
Sakic, Boris
Zoopharmacognosy in Diseased Laboratory Mice: Conflicting Evidence
title Zoopharmacognosy in Diseased Laboratory Mice: Conflicting Evidence
title_full Zoopharmacognosy in Diseased Laboratory Mice: Conflicting Evidence
title_fullStr Zoopharmacognosy in Diseased Laboratory Mice: Conflicting Evidence
title_full_unstemmed Zoopharmacognosy in Diseased Laboratory Mice: Conflicting Evidence
title_short Zoopharmacognosy in Diseased Laboratory Mice: Conflicting Evidence
title_sort zoopharmacognosy in diseased laboratory mice: conflicting evidence
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4067353/
https://www.ncbi.nlm.nih.gov/pubmed/24956477
http://dx.doi.org/10.1371/journal.pone.0100684
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