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Effect Neonatal Ketamine Treatment on Exploratory and Anxiety-like Behaviours in Adulthood
OBJECTIVE: In this study, we evaluated the effect of neonatal ketamine exposure on anxiety-like and exploratory behaviours in adult the Balb/c and C57BL/6 strains of mice which anxiety responses are different. METHODS: Ketamine was administered at two different doses single dose (10, 20 mg/kg, 0.1 m...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean College of Neuropsychopharmacology
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7851452/ https://www.ncbi.nlm.nih.gov/pubmed/33508792 http://dx.doi.org/10.9758/cpn.2021.19.1.93 |
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author | Akillioglu, Kübra Karadepe, Mustafa |
author_facet | Akillioglu, Kübra Karadepe, Mustafa |
author_sort | Akillioglu, Kübra |
collection | PubMed |
description | OBJECTIVE: In this study, we evaluated the effect of neonatal ketamine exposure on anxiety-like and exploratory behaviours in adult the Balb/c and C57BL/6 strains of mice which anxiety responses are different. METHODS: Ketamine was administered at two different doses single dose (10, 20 mg/kg, 0.1 ml/10 g body weight, intraperitoneally) and repeated doses (10, 20 mg/kg every 240 minutes; thrice times) on the 7th postnatal day to male Balb/c and C57BL/6 mice. In adulthood, open-field (OF) and elevated plus maze (EPM) apparatuses were used to evaluate exploratory and anxiety-like behaviour. RESULTS: In the C57BL/6 mice, the 20 mg/kg single dose decreased open-arm time and total-arm entries in EPM and increased time of central latency and decreased distance travelled in OF. Both the 10 and 20 mg/kg repetitive doses increased time of central latency and decreased time spent in the centre, frequency of rearing and centre crossing in OF and decreased open-arm time, total-arm entries, number of open-arm entries in EPM. The 20 mg/kg repetitive dose decreased number of head dipping behaviours in EPM. In the Balb/c mice, both the single and repetitive 10−20 mg/kg doses had no significant effect on anxiety-like and exploratory behaviours. CONCLUSION: There were no significant differences in anxiety-like and exploratory behaviour in different strains by the single 10 mg/kg dose. However, in the C57BL/6 mice, both the single and repetitive 20 mg/kg doses and the 10 mg/kg repetitive dose increased anxiety-like behaviour and decreased exploratory behaviour in EPM and OF. In conclusion, hereditary factors may be effective on the effect of neonatal ketamine treatment on anxiety-like and exploratory behaviour. |
format | Online Article Text |
id | pubmed-7851452 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Korean College of Neuropsychopharmacology |
record_format | MEDLINE/PubMed |
spelling | pubmed-78514522021-02-28 Effect Neonatal Ketamine Treatment on Exploratory and Anxiety-like Behaviours in Adulthood Akillioglu, Kübra Karadepe, Mustafa Clin Psychopharmacol Neurosci Original Article OBJECTIVE: In this study, we evaluated the effect of neonatal ketamine exposure on anxiety-like and exploratory behaviours in adult the Balb/c and C57BL/6 strains of mice which anxiety responses are different. METHODS: Ketamine was administered at two different doses single dose (10, 20 mg/kg, 0.1 ml/10 g body weight, intraperitoneally) and repeated doses (10, 20 mg/kg every 240 minutes; thrice times) on the 7th postnatal day to male Balb/c and C57BL/6 mice. In adulthood, open-field (OF) and elevated plus maze (EPM) apparatuses were used to evaluate exploratory and anxiety-like behaviour. RESULTS: In the C57BL/6 mice, the 20 mg/kg single dose decreased open-arm time and total-arm entries in EPM and increased time of central latency and decreased distance travelled in OF. Both the 10 and 20 mg/kg repetitive doses increased time of central latency and decreased time spent in the centre, frequency of rearing and centre crossing in OF and decreased open-arm time, total-arm entries, number of open-arm entries in EPM. The 20 mg/kg repetitive dose decreased number of head dipping behaviours in EPM. In the Balb/c mice, both the single and repetitive 10−20 mg/kg doses had no significant effect on anxiety-like and exploratory behaviours. CONCLUSION: There were no significant differences in anxiety-like and exploratory behaviour in different strains by the single 10 mg/kg dose. However, in the C57BL/6 mice, both the single and repetitive 20 mg/kg doses and the 10 mg/kg repetitive dose increased anxiety-like behaviour and decreased exploratory behaviour in EPM and OF. In conclusion, hereditary factors may be effective on the effect of neonatal ketamine treatment on anxiety-like and exploratory behaviour. Korean College of Neuropsychopharmacology 2021-02-28 2021-02-28 /pmc/articles/PMC7851452/ /pubmed/33508792 http://dx.doi.org/10.9758/cpn.2021.19.1.93 Text en Copyright© 2021, Korean College of Neuropsychopharmacology This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Akillioglu, Kübra Karadepe, Mustafa Effect Neonatal Ketamine Treatment on Exploratory and Anxiety-like Behaviours in Adulthood |
title | Effect Neonatal Ketamine Treatment on Exploratory and Anxiety-like Behaviours in Adulthood |
title_full | Effect Neonatal Ketamine Treatment on Exploratory and Anxiety-like Behaviours in Adulthood |
title_fullStr | Effect Neonatal Ketamine Treatment on Exploratory and Anxiety-like Behaviours in Adulthood |
title_full_unstemmed | Effect Neonatal Ketamine Treatment on Exploratory and Anxiety-like Behaviours in Adulthood |
title_short | Effect Neonatal Ketamine Treatment on Exploratory and Anxiety-like Behaviours in Adulthood |
title_sort | effect neonatal ketamine treatment on exploratory and anxiety-like behaviours in adulthood |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7851452/ https://www.ncbi.nlm.nih.gov/pubmed/33508792 http://dx.doi.org/10.9758/cpn.2021.19.1.93 |
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