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Acute ethanol treatment upregulates th1, th2, and hdc in larval zebrafish in stable networks
Earlier studies in zebrafish have revealed that acutely given ethanol has a stimulatory effect on locomotion in fish larvae but the mechanism of this effect has not been revealed. We studied the effects of ethanol concentrations between 0.75 and 3.00% on 7-day-old larval zebrafish (Danio rerio) of t...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3668275/ https://www.ncbi.nlm.nih.gov/pubmed/23754986 http://dx.doi.org/10.3389/fncir.2013.00102 |
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author | Puttonen, Henri A. J. Sundvik, Maria Rozov, Stanislav Chen, Yu-Chia Panula, Pertti |
author_facet | Puttonen, Henri A. J. Sundvik, Maria Rozov, Stanislav Chen, Yu-Chia Panula, Pertti |
author_sort | Puttonen, Henri A. J. |
collection | PubMed |
description | Earlier studies in zebrafish have revealed that acutely given ethanol has a stimulatory effect on locomotion in fish larvae but the mechanism of this effect has not been revealed. We studied the effects of ethanol concentrations between 0.75 and 3.00% on 7-day-old larval zebrafish (Danio rerio) of the Turku strain. At 0.75-3% concentrations ethanol increased swimming speed during the first minute. At 3% the swimming speed decreased rapidly after the first minute, whereas at 0.75 and 1.5% a prolonged increase in swimming speed was seen. At the highest ethanol concentration dopamine levels decreased significantly after a 10-min treatment. We found that ethanol upregulates key genes involved in the biosynthesis of histamine (hdc) and dopamine (th1 and th2) following a short 10-min ethanol treatment, measured by qPCR. Using in situ hybridization and immunohistochemistry, we further discovered that the morphology of the histaminergic and dopaminergic neurons and networks in the larval zebrafish brain was unaffected by both the 10-min and a longer 30-min treatment. The results suggest that acute ethanol rapidly decreases dopamine levels, and activates both forms or th to replenish the dopamine stores within 30 min. The dynamic changes in histaminergic and dopaminergic system enzymes occurred in the same cells which normally express the transcripts. As both dopamine and histamine are known to be involved in the behavioral effects of ethanol and locomotor stimulation, these results suggest that rapid adaptations of these networks are associated with altered locomotor activity. |
format | Online Article Text |
id | pubmed-3668275 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-36682752013-06-10 Acute ethanol treatment upregulates th1, th2, and hdc in larval zebrafish in stable networks Puttonen, Henri A. J. Sundvik, Maria Rozov, Stanislav Chen, Yu-Chia Panula, Pertti Front Neural Circuits Neuroscience Earlier studies in zebrafish have revealed that acutely given ethanol has a stimulatory effect on locomotion in fish larvae but the mechanism of this effect has not been revealed. We studied the effects of ethanol concentrations between 0.75 and 3.00% on 7-day-old larval zebrafish (Danio rerio) of the Turku strain. At 0.75-3% concentrations ethanol increased swimming speed during the first minute. At 3% the swimming speed decreased rapidly after the first minute, whereas at 0.75 and 1.5% a prolonged increase in swimming speed was seen. At the highest ethanol concentration dopamine levels decreased significantly after a 10-min treatment. We found that ethanol upregulates key genes involved in the biosynthesis of histamine (hdc) and dopamine (th1 and th2) following a short 10-min ethanol treatment, measured by qPCR. Using in situ hybridization and immunohistochemistry, we further discovered that the morphology of the histaminergic and dopaminergic neurons and networks in the larval zebrafish brain was unaffected by both the 10-min and a longer 30-min treatment. The results suggest that acute ethanol rapidly decreases dopamine levels, and activates both forms or th to replenish the dopamine stores within 30 min. The dynamic changes in histaminergic and dopaminergic system enzymes occurred in the same cells which normally express the transcripts. As both dopamine and histamine are known to be involved in the behavioral effects of ethanol and locomotor stimulation, these results suggest that rapid adaptations of these networks are associated with altered locomotor activity. Frontiers Media S.A. 2013-05-31 /pmc/articles/PMC3668275/ /pubmed/23754986 http://dx.doi.org/10.3389/fncir.2013.00102 Text en Copyright © 2013 Puttonen, Sundvik, Rozov, Chen, and Panula. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc. |
spellingShingle | Neuroscience Puttonen, Henri A. J. Sundvik, Maria Rozov, Stanislav Chen, Yu-Chia Panula, Pertti Acute ethanol treatment upregulates th1, th2, and hdc in larval zebrafish in stable networks |
title | Acute ethanol treatment upregulates th1, th2, and hdc in larval zebrafish in stable networks |
title_full | Acute ethanol treatment upregulates th1, th2, and hdc in larval zebrafish in stable networks |
title_fullStr | Acute ethanol treatment upregulates th1, th2, and hdc in larval zebrafish in stable networks |
title_full_unstemmed | Acute ethanol treatment upregulates th1, th2, and hdc in larval zebrafish in stable networks |
title_short | Acute ethanol treatment upregulates th1, th2, and hdc in larval zebrafish in stable networks |
title_sort | acute ethanol treatment upregulates th1, th2, and hdc in larval zebrafish in stable networks |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3668275/ https://www.ncbi.nlm.nih.gov/pubmed/23754986 http://dx.doi.org/10.3389/fncir.2013.00102 |
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