Cargando…

Critical Effects on Akt Signaling in Adult Zebrafish Brain Following Alterations in Light Exposure

Evidence from human and animal studies indicate that disrupted light cycles leads to alterations of the sleep state, poor cognition, and the risk of developing neuroinflammatory and generalized health disorders. Zebrafish exhibit a diurnal circadian rhythm and are an increasingly popular model in st...

Descripción completa

Detalles Bibliográficos
Autores principales: Moore, Nicholas S., Mans, Robert A., McCauley, Mackenzee K., Allgood, Colton S., Barksdale, Keri A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8000057/
https://www.ncbi.nlm.nih.gov/pubmed/33809219
http://dx.doi.org/10.3390/cells10030637
_version_ 1783670919036665856
author Moore, Nicholas S.
Mans, Robert A.
McCauley, Mackenzee K.
Allgood, Colton S.
Barksdale, Keri A.
author_facet Moore, Nicholas S.
Mans, Robert A.
McCauley, Mackenzee K.
Allgood, Colton S.
Barksdale, Keri A.
author_sort Moore, Nicholas S.
collection PubMed
description Evidence from human and animal studies indicate that disrupted light cycles leads to alterations of the sleep state, poor cognition, and the risk of developing neuroinflammatory and generalized health disorders. Zebrafish exhibit a diurnal circadian rhythm and are an increasingly popular model in studies of neurophysiology and neuropathophysiology. Here, we investigate the effect of alterations in light cycle on the adult zebrafish brain: we measured the effect of altered, unpredictable light exposure in adult zebrafish telencephalon, homologous to mammalian hippocampus, and the optic tectum, a significant visual processing center with extensive telencephalon connections. The expression of heat shock protein-70 (HSP70), an important cell stress mediator, was significantly decreased in optic tectum of adult zebrafish brain following four days of altered light exposure. Further, pSer473-Akt (protein kinase B) was significantly reduced in telencephalon following light cycle alteration, and pSer9-GSK3β (glycogen synthase kinase-3β) was significantly reduced in both the telencephalon and optic tectum of light-altered fish. Animals exposed to five minutes of environmental enrichment showed significant increase in pSer473Akt, which was significantly attenuated by four days of altered light exposure. These data show for the first time that unpredictable light exposure alters HSP70 expression and dysregulates Akt-GSK3β signaling in the adult zebrafish brain.
format Online
Article
Text
id pubmed-8000057
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-80000572021-03-28 Critical Effects on Akt Signaling in Adult Zebrafish Brain Following Alterations in Light Exposure Moore, Nicholas S. Mans, Robert A. McCauley, Mackenzee K. Allgood, Colton S. Barksdale, Keri A. Cells Communication Evidence from human and animal studies indicate that disrupted light cycles leads to alterations of the sleep state, poor cognition, and the risk of developing neuroinflammatory and generalized health disorders. Zebrafish exhibit a diurnal circadian rhythm and are an increasingly popular model in studies of neurophysiology and neuropathophysiology. Here, we investigate the effect of alterations in light cycle on the adult zebrafish brain: we measured the effect of altered, unpredictable light exposure in adult zebrafish telencephalon, homologous to mammalian hippocampus, and the optic tectum, a significant visual processing center with extensive telencephalon connections. The expression of heat shock protein-70 (HSP70), an important cell stress mediator, was significantly decreased in optic tectum of adult zebrafish brain following four days of altered light exposure. Further, pSer473-Akt (protein kinase B) was significantly reduced in telencephalon following light cycle alteration, and pSer9-GSK3β (glycogen synthase kinase-3β) was significantly reduced in both the telencephalon and optic tectum of light-altered fish. Animals exposed to five minutes of environmental enrichment showed significant increase in pSer473Akt, which was significantly attenuated by four days of altered light exposure. These data show for the first time that unpredictable light exposure alters HSP70 expression and dysregulates Akt-GSK3β signaling in the adult zebrafish brain. MDPI 2021-03-12 /pmc/articles/PMC8000057/ /pubmed/33809219 http://dx.doi.org/10.3390/cells10030637 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Communication
Moore, Nicholas S.
Mans, Robert A.
McCauley, Mackenzee K.
Allgood, Colton S.
Barksdale, Keri A.
Critical Effects on Akt Signaling in Adult Zebrafish Brain Following Alterations in Light Exposure
title Critical Effects on Akt Signaling in Adult Zebrafish Brain Following Alterations in Light Exposure
title_full Critical Effects on Akt Signaling in Adult Zebrafish Brain Following Alterations in Light Exposure
title_fullStr Critical Effects on Akt Signaling in Adult Zebrafish Brain Following Alterations in Light Exposure
title_full_unstemmed Critical Effects on Akt Signaling in Adult Zebrafish Brain Following Alterations in Light Exposure
title_short Critical Effects on Akt Signaling in Adult Zebrafish Brain Following Alterations in Light Exposure
title_sort critical effects on akt signaling in adult zebrafish brain following alterations in light exposure
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8000057/
https://www.ncbi.nlm.nih.gov/pubmed/33809219
http://dx.doi.org/10.3390/cells10030637
work_keys_str_mv AT moorenicholass criticaleffectsonaktsignalinginadultzebrafishbrainfollowingalterationsinlightexposure
AT mansroberta criticaleffectsonaktsignalinginadultzebrafishbrainfollowingalterationsinlightexposure
AT mccauleymackenzeek criticaleffectsonaktsignalinginadultzebrafishbrainfollowingalterationsinlightexposure
AT allgoodcoltons criticaleffectsonaktsignalinginadultzebrafishbrainfollowingalterationsinlightexposure
AT barksdalekeria criticaleffectsonaktsignalinginadultzebrafishbrainfollowingalterationsinlightexposure