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UV irradiation to mouse skin decreases hippocampal neurogenesis and synaptic protein expression via HPA axis activation

The skin senses external environment, including ultraviolet light (UV). Hippocampus is a brain region that is responsible for memory and emotion. However, changes in hippocampus by UV irradiation to the skin have not been studied. In this study, after 2 weeks of UV irradiation to the mouse skin, we...

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Autores principales: Han, Mira, Ban, Jae-Jun, Bae, Jung-Soo, Shin, Chang-Yup, Lee, Dong Hun, Chung, Jin Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686175/
https://www.ncbi.nlm.nih.gov/pubmed/29138442
http://dx.doi.org/10.1038/s41598-017-15773-z
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author Han, Mira
Ban, Jae-Jun
Bae, Jung-Soo
Shin, Chang-Yup
Lee, Dong Hun
Chung, Jin Ho
author_facet Han, Mira
Ban, Jae-Jun
Bae, Jung-Soo
Shin, Chang-Yup
Lee, Dong Hun
Chung, Jin Ho
author_sort Han, Mira
collection PubMed
description The skin senses external environment, including ultraviolet light (UV). Hippocampus is a brain region that is responsible for memory and emotion. However, changes in hippocampus by UV irradiation to the skin have not been studied. In this study, after 2 weeks of UV irradiation to the mouse skin, we examined molecular changes related to cognitive functions in the hippocampus and activation of the hypothalamic-pituitary-adrenal (HPA) axis. UV exposure to the skin decreased doublecortin-positive immature neurons and synaptic proteins, including N-methyl-D-aspartate receptor 2 A and postsynaptic density protein-95, in the hippocampus. Moreover, we observed that UV irradiation to the skin down-regulated brain-derived neurotrophic factor expression and ERK signaling in the hippocampus, which are known to modulate neurogenesis and synaptic plasticity. The cutaneous and central HPA axes were activated by UV, which resulted in significant increases in serum levels of corticosterone. Subsequently, UV irradiation to the skin activated the glucocorticoid-signaling pathway in the hippocampal dentate gyrus. Interestingly, after 6 weeks of UV irradiation, mice showed depression-like behavior in the tail suspension test. Taken together, our data suggest that repeated UV exposure through the skin may negatively affect hippocampal neurogenesis and synaptic plasticity along with HPA axis activation.
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spelling pubmed-56861752017-11-21 UV irradiation to mouse skin decreases hippocampal neurogenesis and synaptic protein expression via HPA axis activation Han, Mira Ban, Jae-Jun Bae, Jung-Soo Shin, Chang-Yup Lee, Dong Hun Chung, Jin Ho Sci Rep Article The skin senses external environment, including ultraviolet light (UV). Hippocampus is a brain region that is responsible for memory and emotion. However, changes in hippocampus by UV irradiation to the skin have not been studied. In this study, after 2 weeks of UV irradiation to the mouse skin, we examined molecular changes related to cognitive functions in the hippocampus and activation of the hypothalamic-pituitary-adrenal (HPA) axis. UV exposure to the skin decreased doublecortin-positive immature neurons and synaptic proteins, including N-methyl-D-aspartate receptor 2 A and postsynaptic density protein-95, in the hippocampus. Moreover, we observed that UV irradiation to the skin down-regulated brain-derived neurotrophic factor expression and ERK signaling in the hippocampus, which are known to modulate neurogenesis and synaptic plasticity. The cutaneous and central HPA axes were activated by UV, which resulted in significant increases in serum levels of corticosterone. Subsequently, UV irradiation to the skin activated the glucocorticoid-signaling pathway in the hippocampal dentate gyrus. Interestingly, after 6 weeks of UV irradiation, mice showed depression-like behavior in the tail suspension test. Taken together, our data suggest that repeated UV exposure through the skin may negatively affect hippocampal neurogenesis and synaptic plasticity along with HPA axis activation. Nature Publishing Group UK 2017-11-14 /pmc/articles/PMC5686175/ /pubmed/29138442 http://dx.doi.org/10.1038/s41598-017-15773-z Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Han, Mira
Ban, Jae-Jun
Bae, Jung-Soo
Shin, Chang-Yup
Lee, Dong Hun
Chung, Jin Ho
UV irradiation to mouse skin decreases hippocampal neurogenesis and synaptic protein expression via HPA axis activation
title UV irradiation to mouse skin decreases hippocampal neurogenesis and synaptic protein expression via HPA axis activation
title_full UV irradiation to mouse skin decreases hippocampal neurogenesis and synaptic protein expression via HPA axis activation
title_fullStr UV irradiation to mouse skin decreases hippocampal neurogenesis and synaptic protein expression via HPA axis activation
title_full_unstemmed UV irradiation to mouse skin decreases hippocampal neurogenesis and synaptic protein expression via HPA axis activation
title_short UV irradiation to mouse skin decreases hippocampal neurogenesis and synaptic protein expression via HPA axis activation
title_sort uv irradiation to mouse skin decreases hippocampal neurogenesis and synaptic protein expression via hpa axis activation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686175/
https://www.ncbi.nlm.nih.gov/pubmed/29138442
http://dx.doi.org/10.1038/s41598-017-15773-z
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