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Caffeine improves bladder function in diabetic rats via a neuroprotective effect
Diabetic cystopathy (DCP) is one of the most common complications of diabetes mellitus (DM). A previous study reported that caffeine may improve bladder dysfunction in rats with DM. The aim of the present study was to investigate the mechanisms behind the capacity for caffeine to improve bladder fun...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8005692/ https://www.ncbi.nlm.nih.gov/pubmed/33791010 http://dx.doi.org/10.3892/etm.2021.9932 |
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author | Xue, Jun Liu, Yadong Zhang, Sichong Ding, Liucheng Shen, Baixin Shao, Yunpeng Wei, Zhongqing |
author_facet | Xue, Jun Liu, Yadong Zhang, Sichong Ding, Liucheng Shen, Baixin Shao, Yunpeng Wei, Zhongqing |
author_sort | Xue, Jun |
collection | PubMed |
description | Diabetic cystopathy (DCP) is one of the most common complications of diabetes mellitus (DM). A previous study reported that caffeine may improve bladder dysfunction in rats with DM. The aim of the present study was to investigate the mechanisms behind the capacity for caffeine to improve bladder function in rats with DM. Sprague Dawley rats were divided into four groups: control, caffeine, DM and DM plus caffeine treatment (DM + caffeine). Bladder function was measured by urodynamic analyses. The levels of nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF) and calcitonin gene-related peptide (CGRP) in the bladder tissue were detected by ELISA. Apoptosis in the dorsal root ganglion (DRG) was detected by terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling assay. The expression levels of B-cell lymphoma-2 (Bcl-2), Bcl-2-associated X protein (Bax), caspase-3, cleaved caspase-3, caspase-9 and cleaved caspase-9 proteins in the DRG were detected by western blotting. Following treatment with caffeine, the urination time and micturition interval of rats with DM were improved, the bladder wet weight was decreased, and the maximum voiding pressure was increased. Relative to that in the DM group, the expression levels of NGF, BDNF and CGRP in the bladder tissue of DM + caffeine rats increased; cellular apoptosis in the DRG of DM + caffeine rates decreased; and the expression levels of Bcl-2, Bax, cleaved caspase-3 and cleaved caspase-9 proteins in the DRG of DM + caffeine rats were restored to a certain extent. In conclusion, caffeine promotes bladder function in rats with DM through a protective effect on DRG. |
format | Online Article Text |
id | pubmed-8005692 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-80056922021-03-30 Caffeine improves bladder function in diabetic rats via a neuroprotective effect Xue, Jun Liu, Yadong Zhang, Sichong Ding, Liucheng Shen, Baixin Shao, Yunpeng Wei, Zhongqing Exp Ther Med Articles Diabetic cystopathy (DCP) is one of the most common complications of diabetes mellitus (DM). A previous study reported that caffeine may improve bladder dysfunction in rats with DM. The aim of the present study was to investigate the mechanisms behind the capacity for caffeine to improve bladder function in rats with DM. Sprague Dawley rats were divided into four groups: control, caffeine, DM and DM plus caffeine treatment (DM + caffeine). Bladder function was measured by urodynamic analyses. The levels of nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF) and calcitonin gene-related peptide (CGRP) in the bladder tissue were detected by ELISA. Apoptosis in the dorsal root ganglion (DRG) was detected by terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling assay. The expression levels of B-cell lymphoma-2 (Bcl-2), Bcl-2-associated X protein (Bax), caspase-3, cleaved caspase-3, caspase-9 and cleaved caspase-9 proteins in the DRG were detected by western blotting. Following treatment with caffeine, the urination time and micturition interval of rats with DM were improved, the bladder wet weight was decreased, and the maximum voiding pressure was increased. Relative to that in the DM group, the expression levels of NGF, BDNF and CGRP in the bladder tissue of DM + caffeine rats increased; cellular apoptosis in the DRG of DM + caffeine rates decreased; and the expression levels of Bcl-2, Bax, cleaved caspase-3 and cleaved caspase-9 proteins in the DRG of DM + caffeine rats were restored to a certain extent. In conclusion, caffeine promotes bladder function in rats with DM through a protective effect on DRG. D.A. Spandidos 2021-05 2021-03-17 /pmc/articles/PMC8005692/ /pubmed/33791010 http://dx.doi.org/10.3892/etm.2021.9932 Text en Copyright: © Xue et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Xue, Jun Liu, Yadong Zhang, Sichong Ding, Liucheng Shen, Baixin Shao, Yunpeng Wei, Zhongqing Caffeine improves bladder function in diabetic rats via a neuroprotective effect |
title | Caffeine improves bladder function in diabetic rats via a neuroprotective effect |
title_full | Caffeine improves bladder function in diabetic rats via a neuroprotective effect |
title_fullStr | Caffeine improves bladder function in diabetic rats via a neuroprotective effect |
title_full_unstemmed | Caffeine improves bladder function in diabetic rats via a neuroprotective effect |
title_short | Caffeine improves bladder function in diabetic rats via a neuroprotective effect |
title_sort | caffeine improves bladder function in diabetic rats via a neuroprotective effect |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8005692/ https://www.ncbi.nlm.nih.gov/pubmed/33791010 http://dx.doi.org/10.3892/etm.2021.9932 |
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