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Bladder outlet obstruction disrupts circadian bladder function in mice

The circadian clock programs daily rhythms and coordinates multiple behavioural processes, including micturition. Partial bladder outlet obstruction (pBOO) in mice produces hyperactive voiding. However, long-term effects of pBOO on bladder function have not been clarified. In this study, we investig...

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Autores principales: Kitta, Takeya, Chiba, Hiroki, Kanno, Yukiko, Hattori, Tsuyoshi, Higuchi, Madoka, Ouchi, Mifuka, Togo, Mio, Takahashi, Yui, Michishita, Mai, Kitano, Tatsuya, Shinohara, Nobuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7360733/
https://www.ncbi.nlm.nih.gov/pubmed/32665549
http://dx.doi.org/10.1038/s41598-020-68499-w
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author Kitta, Takeya
Chiba, Hiroki
Kanno, Yukiko
Hattori, Tsuyoshi
Higuchi, Madoka
Ouchi, Mifuka
Togo, Mio
Takahashi, Yui
Michishita, Mai
Kitano, Tatsuya
Shinohara, Nobuo
author_facet Kitta, Takeya
Chiba, Hiroki
Kanno, Yukiko
Hattori, Tsuyoshi
Higuchi, Madoka
Ouchi, Mifuka
Togo, Mio
Takahashi, Yui
Michishita, Mai
Kitano, Tatsuya
Shinohara, Nobuo
author_sort Kitta, Takeya
collection PubMed
description The circadian clock programs daily rhythms and coordinates multiple behavioural processes, including micturition. Partial bladder outlet obstruction (pBOO) in mice produces hyperactive voiding. However, long-term effects of pBOO on bladder function have not been clarified. In this study, we investigated micturition under conditions of impaired circadian bladder function by inducing long-term pBOO by tying the proximal urethra. Micturition behavior was evaluated at 1, 3, 6 and 12 months after surgery. We used automated voided stain on paper method for a precise micturition recording for mice. And quantitative assessment of gene expression was performed at 24 months after pBOO surgery using qRT-PCR procedure. The micturition frequencies in the pBOO group were significantly decreased at 3, 6, and 12 months compared to those at 1 month after operation in the same group (p < 0.05). Body weight of pBOO mice was significantly increased compared to sham operated mice at 12 months. The expression level of mRNA was exhibited a 3.4-fold nominal increased for a 5-HT2B receptor in the pBOO group compared to the sham group. The current study found that long-term pBOO led to disruption of the circadian bladder function (the day/night cycle) in mice, similar to those observed in human as nocturia. This disruption is possible involvement of the gain of body weight and/or serotonergic alteration after pBOO.
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spelling pubmed-73607332020-07-16 Bladder outlet obstruction disrupts circadian bladder function in mice Kitta, Takeya Chiba, Hiroki Kanno, Yukiko Hattori, Tsuyoshi Higuchi, Madoka Ouchi, Mifuka Togo, Mio Takahashi, Yui Michishita, Mai Kitano, Tatsuya Shinohara, Nobuo Sci Rep Article The circadian clock programs daily rhythms and coordinates multiple behavioural processes, including micturition. Partial bladder outlet obstruction (pBOO) in mice produces hyperactive voiding. However, long-term effects of pBOO on bladder function have not been clarified. In this study, we investigated micturition under conditions of impaired circadian bladder function by inducing long-term pBOO by tying the proximal urethra. Micturition behavior was evaluated at 1, 3, 6 and 12 months after surgery. We used automated voided stain on paper method for a precise micturition recording for mice. And quantitative assessment of gene expression was performed at 24 months after pBOO surgery using qRT-PCR procedure. The micturition frequencies in the pBOO group were significantly decreased at 3, 6, and 12 months compared to those at 1 month after operation in the same group (p < 0.05). Body weight of pBOO mice was significantly increased compared to sham operated mice at 12 months. The expression level of mRNA was exhibited a 3.4-fold nominal increased for a 5-HT2B receptor in the pBOO group compared to the sham group. The current study found that long-term pBOO led to disruption of the circadian bladder function (the day/night cycle) in mice, similar to those observed in human as nocturia. This disruption is possible involvement of the gain of body weight and/or serotonergic alteration after pBOO. Nature Publishing Group UK 2020-07-14 /pmc/articles/PMC7360733/ /pubmed/32665549 http://dx.doi.org/10.1038/s41598-020-68499-w Text en © The Author(s) 2020 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
Kitta, Takeya
Chiba, Hiroki
Kanno, Yukiko
Hattori, Tsuyoshi
Higuchi, Madoka
Ouchi, Mifuka
Togo, Mio
Takahashi, Yui
Michishita, Mai
Kitano, Tatsuya
Shinohara, Nobuo
Bladder outlet obstruction disrupts circadian bladder function in mice
title Bladder outlet obstruction disrupts circadian bladder function in mice
title_full Bladder outlet obstruction disrupts circadian bladder function in mice
title_fullStr Bladder outlet obstruction disrupts circadian bladder function in mice
title_full_unstemmed Bladder outlet obstruction disrupts circadian bladder function in mice
title_short Bladder outlet obstruction disrupts circadian bladder function in mice
title_sort bladder outlet obstruction disrupts circadian bladder function in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7360733/
https://www.ncbi.nlm.nih.gov/pubmed/32665549
http://dx.doi.org/10.1038/s41598-020-68499-w
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