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Foraging enrichment modulates open field response to monosodium glutamate in mice
BACKGROUND: Environmental enrichment can enhance expression of species-specific behaviour. While foraging enrichment is encouraged in laboratory animals, its impact on novelty induced behaviour remain largely unknown. PURPOSE: Here, we studied behavioural response of mice to acute and subchronic ora...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Indian Academy of Neurosciences
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4481551/ https://www.ncbi.nlm.nih.gov/pubmed/26130924 http://dx.doi.org/10.5214/ans.0972.7531.220306 |
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author | Onaolapo, Olakunle J Onaolapo, Adejoke Y Akanmu, Moses A Olayiwola, Gbola |
author_facet | Onaolapo, Olakunle J Onaolapo, Adejoke Y Akanmu, Moses A Olayiwola, Gbola |
author_sort | Onaolapo, Olakunle J |
collection | PubMed |
description | BACKGROUND: Environmental enrichment can enhance expression of species-specific behaviour. While foraging enrichment is encouraged in laboratory animals, its impact on novelty induced behaviour remain largely unknown. PURPOSE: Here, we studied behavioural response of mice to acute and subchronic oral monosodium glutamate (MSG) in an open field with /without foraging enrichment. METHODS: Adult male mice, assigned to five groups were administered vehicle (distilled water), or one of four selected doses of MSG (10, 20, 40 and 80 mg/kg) for 21 days. Open field novelty induced behaviours i.e. horizontal locomotion, rearing and grooming were assessed after the first and last doses of MSG. Results were analysed using MANOVA followed by Tukey HSD multiple comparison test and expressed as mean ± S.E.M. RESULTS: Following acute MSG administration without enrichment, locomotor activity reduced, grooming increased, while rearing activity reduced at lower doses and increased at higher doses. Subchronic administration without enrichment was associated with increased locomotor activity and reduction in grooming, rearing activity however still showed a biphasic response. Addition of enrichment with acute administration resulted in sustained reduction in locomotor and rearing activities with a biphasic grooming response. Subchronically, there was reduction in horizontal locomotion, biphasic rearing response and sustained increase in grooming activity. CONCLUSION: Behavioural response to varying doses of MSG as observed in the open field is affected by modifications such as foraging enrichment, which can reverse or dampen the central effects seen irrespective of duration of administration. |
format | Online Article Text |
id | pubmed-4481551 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Indian Academy of Neurosciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-44815512015-07-01 Foraging enrichment modulates open field response to monosodium glutamate in mice Onaolapo, Olakunle J Onaolapo, Adejoke Y Akanmu, Moses A Olayiwola, Gbola Ann Neurosci Research Article BACKGROUND: Environmental enrichment can enhance expression of species-specific behaviour. While foraging enrichment is encouraged in laboratory animals, its impact on novelty induced behaviour remain largely unknown. PURPOSE: Here, we studied behavioural response of mice to acute and subchronic oral monosodium glutamate (MSG) in an open field with /without foraging enrichment. METHODS: Adult male mice, assigned to five groups were administered vehicle (distilled water), or one of four selected doses of MSG (10, 20, 40 and 80 mg/kg) for 21 days. Open field novelty induced behaviours i.e. horizontal locomotion, rearing and grooming were assessed after the first and last doses of MSG. Results were analysed using MANOVA followed by Tukey HSD multiple comparison test and expressed as mean ± S.E.M. RESULTS: Following acute MSG administration without enrichment, locomotor activity reduced, grooming increased, while rearing activity reduced at lower doses and increased at higher doses. Subchronic administration without enrichment was associated with increased locomotor activity and reduction in grooming, rearing activity however still showed a biphasic response. Addition of enrichment with acute administration resulted in sustained reduction in locomotor and rearing activities with a biphasic grooming response. Subchronically, there was reduction in horizontal locomotion, biphasic rearing response and sustained increase in grooming activity. CONCLUSION: Behavioural response to varying doses of MSG as observed in the open field is affected by modifications such as foraging enrichment, which can reverse or dampen the central effects seen irrespective of duration of administration. Indian Academy of Neurosciences 2015-07 /pmc/articles/PMC4481551/ /pubmed/26130924 http://dx.doi.org/10.5214/ans.0972.7531.220306 Text en Copyright © 2015, The National Academy of Sciences http://creativecommons.org/licenses/by-nc-nd/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 work is properly cited. |
spellingShingle | Research Article Onaolapo, Olakunle J Onaolapo, Adejoke Y Akanmu, Moses A Olayiwola, Gbola Foraging enrichment modulates open field response to monosodium glutamate in mice |
title | Foraging enrichment modulates open field response to monosodium glutamate in mice |
title_full | Foraging enrichment modulates open field response to monosodium glutamate in mice |
title_fullStr | Foraging enrichment modulates open field response to monosodium glutamate in mice |
title_full_unstemmed | Foraging enrichment modulates open field response to monosodium glutamate in mice |
title_short | Foraging enrichment modulates open field response to monosodium glutamate in mice |
title_sort | foraging enrichment modulates open field response to monosodium glutamate in mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4481551/ https://www.ncbi.nlm.nih.gov/pubmed/26130924 http://dx.doi.org/10.5214/ans.0972.7531.220306 |
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