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Changes of Locomotor Activity by Dopamine D2, D3 Agonist Quinpirole in Mice Using Home-cage Monitoring System

OBJECTIVE: As dopamine is closely linked to locomotor activities, animal studies on locomotor activities using dopaminergic agents were widely done. However, most of animal studies were performed for a short period that there is a lack of longitudinal study on the effects of dopaminergic agents on l...

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Autores principales: Park, Jeonghyun, Moon, Eunsoo, Lim, Hyun Ju, Kim, Kyungwon, Hong, Yoo Rha, Lee, Jung Hyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean College of Neuropsychopharmacology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10591172/
https://www.ncbi.nlm.nih.gov/pubmed/37859441
http://dx.doi.org/10.9758/cpn.22.1016
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author Park, Jeonghyun
Moon, Eunsoo
Lim, Hyun Ju
Kim, Kyungwon
Hong, Yoo Rha
Lee, Jung Hyun
author_facet Park, Jeonghyun
Moon, Eunsoo
Lim, Hyun Ju
Kim, Kyungwon
Hong, Yoo Rha
Lee, Jung Hyun
author_sort Park, Jeonghyun
collection PubMed
description OBJECTIVE: As dopamine is closely linked to locomotor activities, animal studies on locomotor activities using dopaminergic agents were widely done. However, most of animal studies were performed for a short period that there is a lack of longitudinal study on the effects of dopaminergic agents on locomotor activities. This study aimed to examine the long- term effect of a dopamine D2, D3 agonist quinpirole on locomotor activities in mice using a home-cage monitoring system. METHODS: The locomotor activities of Institute Cancer Research mice were measured by infrared motion detectors in home-cages under the 12-hour dark and 12-hour light condition for three days after the quinpirole injection. Quinpirole was injected at a concentration of 0.5 mg/kg intraperitoneally in the beginning of the dark phase. The locomotor activities before and after the quinpirole administration were compared by the Wilcoxon signed-rank test and one-way repeated measures ANOVA. RESULTS: After the quinpirole administration, the 24-hour total locomotor activity did not change (p = 0.169), but activities were significantly increased in the 12-hour dark phase sum (p = 0.013) and decreased in the 12-hour light phase sum (p = 0.009). Significant increases in the activities were observed in the dark-light difference (p = 0.005) and dark-light ratio (p = 0.005) as well. CONCLUSION: This study suggests that quinpirole injection entrains the circadian rest-activity rhythm of locomotor activities. Therefore, quinpirole can be a drug that mediates locomotor activity as a dopamine agonist as well as a modulator of the circadian rhythms.
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spelling pubmed-105911722023-10-24 Changes of Locomotor Activity by Dopamine D2, D3 Agonist Quinpirole in Mice Using Home-cage Monitoring System Park, Jeonghyun Moon, Eunsoo Lim, Hyun Ju Kim, Kyungwon Hong, Yoo Rha Lee, Jung Hyun Clin Psychopharmacol Neurosci Original Article OBJECTIVE: As dopamine is closely linked to locomotor activities, animal studies on locomotor activities using dopaminergic agents were widely done. However, most of animal studies were performed for a short period that there is a lack of longitudinal study on the effects of dopaminergic agents on locomotor activities. This study aimed to examine the long- term effect of a dopamine D2, D3 agonist quinpirole on locomotor activities in mice using a home-cage monitoring system. METHODS: The locomotor activities of Institute Cancer Research mice were measured by infrared motion detectors in home-cages under the 12-hour dark and 12-hour light condition for three days after the quinpirole injection. Quinpirole was injected at a concentration of 0.5 mg/kg intraperitoneally in the beginning of the dark phase. The locomotor activities before and after the quinpirole administration were compared by the Wilcoxon signed-rank test and one-way repeated measures ANOVA. RESULTS: After the quinpirole administration, the 24-hour total locomotor activity did not change (p = 0.169), but activities were significantly increased in the 12-hour dark phase sum (p = 0.013) and decreased in the 12-hour light phase sum (p = 0.009). Significant increases in the activities were observed in the dark-light difference (p = 0.005) and dark-light ratio (p = 0.005) as well. CONCLUSION: This study suggests that quinpirole injection entrains the circadian rest-activity rhythm of locomotor activities. Therefore, quinpirole can be a drug that mediates locomotor activity as a dopamine agonist as well as a modulator of the circadian rhythms. Korean College of Neuropsychopharmacology 2023-11-30 2023-05-22 /pmc/articles/PMC10591172/ /pubmed/37859441 http://dx.doi.org/10.9758/cpn.22.1016 Text en Copyright© 2023, Korean College of Neuropsychopharmacology https://creativecommons.org/licenses/by-nc/4.0/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 (https://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
Park, Jeonghyun
Moon, Eunsoo
Lim, Hyun Ju
Kim, Kyungwon
Hong, Yoo Rha
Lee, Jung Hyun
Changes of Locomotor Activity by Dopamine D2, D3 Agonist Quinpirole in Mice Using Home-cage Monitoring System
title Changes of Locomotor Activity by Dopamine D2, D3 Agonist Quinpirole in Mice Using Home-cage Monitoring System
title_full Changes of Locomotor Activity by Dopamine D2, D3 Agonist Quinpirole in Mice Using Home-cage Monitoring System
title_fullStr Changes of Locomotor Activity by Dopamine D2, D3 Agonist Quinpirole in Mice Using Home-cage Monitoring System
title_full_unstemmed Changes of Locomotor Activity by Dopamine D2, D3 Agonist Quinpirole in Mice Using Home-cage Monitoring System
title_short Changes of Locomotor Activity by Dopamine D2, D3 Agonist Quinpirole in Mice Using Home-cage Monitoring System
title_sort changes of locomotor activity by dopamine d2, d3 agonist quinpirole in mice using home-cage monitoring system
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10591172/
https://www.ncbi.nlm.nih.gov/pubmed/37859441
http://dx.doi.org/10.9758/cpn.22.1016
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