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Comparison of neurobehavioral effects of methylmercury exposure in older and younger adult zebrafish (Danio rerio)
It is widely recognized that the nature and severity of responses to toxic exposure are age-dependent. Using active avoidance conditioning as the behavioral paradigm, the present study examined the effect of short-term methylmercury (MeHg) exposure on two adult age classes, 1- and 2-year-olds to coi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8803049/ https://www.ncbi.nlm.nih.gov/pubmed/22796261 http://dx.doi.org/10.1016/j.neuro.2012.06.011 |
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author | Xu, Xiaojuan Weber, Daniel Carvan, Michael J. Coppens, Ryan Lamb, Crystal Goetz, Stefan Schaefer, Lillian A. |
author_facet | Xu, Xiaojuan Weber, Daniel Carvan, Michael J. Coppens, Ryan Lamb, Crystal Goetz, Stefan Schaefer, Lillian A. |
author_sort | Xu, Xiaojuan |
collection | PubMed |
description | It is widely recognized that the nature and severity of responses to toxic exposure are age-dependent. Using active avoidance conditioning as the behavioral paradigm, the present study examined the effect of short-term methylmercury (MeHg) exposure on two adult age classes, 1- and 2-year-olds to coincide with zebrafish in relatively peak vs. declining health conditions. In Experiment 1, 2-year-old zebrafish were randomly divided into groups and were exposed to no MeHg, 0.15% ethanol (EtOH), 0.01, 0.03, 0.1, or 0.3 μM of MeHg (in 0.15% ethanol) for 2 weeks. The groups were then trained and tested for avoidance responses. The results showed that older zebrafish exposed to no MeHg or EtOH learned and retained avoidance responses. However, 0.01 μM or higher concentrations of MeHg exposure impaired avoidance learning in a dose-dependent manner with 0.3 μM of MeHg exposure producing death during the exposure period or shortly after the exposure but before the avoidance training. In Experiment 2, 1-year-old zebrafish were randomly divided into groups and were exposed to the same concentrations of MeHg used in Experiment 1 for 2 weeks. The groups were then trained and tested for avoidance responses. The results showed that younger zebrafish exposed to no MeHg, EtOH, or 0.01 μM of MeHg learned and retained avoidance responses, while 0.1 or 0.3 μM of MeHg exposure impaired avoidance learning in a dose-dependent manner. The study suggested that MeHg exposure produced learning impairments at a much lower concentration of MeHg exposure and more severely in older adult compared against younger adult zebrafish even after short exposure times. |
format | Online Article Text |
id | pubmed-8803049 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
record_format | MEDLINE/PubMed |
spelling | pubmed-88030492022-01-31 Comparison of neurobehavioral effects of methylmercury exposure in older and younger adult zebrafish (Danio rerio) Xu, Xiaojuan Weber, Daniel Carvan, Michael J. Coppens, Ryan Lamb, Crystal Goetz, Stefan Schaefer, Lillian A. Neurotoxicology Article It is widely recognized that the nature and severity of responses to toxic exposure are age-dependent. Using active avoidance conditioning as the behavioral paradigm, the present study examined the effect of short-term methylmercury (MeHg) exposure on two adult age classes, 1- and 2-year-olds to coincide with zebrafish in relatively peak vs. declining health conditions. In Experiment 1, 2-year-old zebrafish were randomly divided into groups and were exposed to no MeHg, 0.15% ethanol (EtOH), 0.01, 0.03, 0.1, or 0.3 μM of MeHg (in 0.15% ethanol) for 2 weeks. The groups were then trained and tested for avoidance responses. The results showed that older zebrafish exposed to no MeHg or EtOH learned and retained avoidance responses. However, 0.01 μM or higher concentrations of MeHg exposure impaired avoidance learning in a dose-dependent manner with 0.3 μM of MeHg exposure producing death during the exposure period or shortly after the exposure but before the avoidance training. In Experiment 2, 1-year-old zebrafish were randomly divided into groups and were exposed to the same concentrations of MeHg used in Experiment 1 for 2 weeks. The groups were then trained and tested for avoidance responses. The results showed that younger zebrafish exposed to no MeHg, EtOH, or 0.01 μM of MeHg learned and retained avoidance responses, while 0.1 or 0.3 μM of MeHg exposure impaired avoidance learning in a dose-dependent manner. The study suggested that MeHg exposure produced learning impairments at a much lower concentration of MeHg exposure and more severely in older adult compared against younger adult zebrafish even after short exposure times. 2012-10 2012-07-13 /pmc/articles/PMC8803049/ /pubmed/22796261 http://dx.doi.org/10.1016/j.neuro.2012.06.011 Text en https://creativecommons.org/licenses/by-nc-nd/3.0/Open access under CC BY-NC-ND license (https://creativecommons.org/licenses/by-nc-nd/3.0/) . |
spellingShingle | Article Xu, Xiaojuan Weber, Daniel Carvan, Michael J. Coppens, Ryan Lamb, Crystal Goetz, Stefan Schaefer, Lillian A. Comparison of neurobehavioral effects of methylmercury exposure in older and younger adult zebrafish (Danio rerio) |
title | Comparison of neurobehavioral effects of methylmercury exposure in older and younger adult zebrafish (Danio rerio) |
title_full | Comparison of neurobehavioral effects of methylmercury exposure in older and younger adult zebrafish (Danio rerio) |
title_fullStr | Comparison of neurobehavioral effects of methylmercury exposure in older and younger adult zebrafish (Danio rerio) |
title_full_unstemmed | Comparison of neurobehavioral effects of methylmercury exposure in older and younger adult zebrafish (Danio rerio) |
title_short | Comparison of neurobehavioral effects of methylmercury exposure in older and younger adult zebrafish (Danio rerio) |
title_sort | comparison of neurobehavioral effects of methylmercury exposure in older and younger adult zebrafish (danio rerio) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8803049/ https://www.ncbi.nlm.nih.gov/pubmed/22796261 http://dx.doi.org/10.1016/j.neuro.2012.06.011 |
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