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An animal study to compare the degree of the suppressive effects on the afferent pathways of micturition between tamsulosin and sildenafil
BACKGROUND: Tamsulosin, an α1-adrenoceptor antagonist, and sildenafil, a phosphodiesterase (PDE) inhibitor, are reported to improve lower urinary tract symptoms including overactive bladder (OAB). This study is aimed at investing the effects of tamsulosin and sildenafil and comparing the degree of t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3871018/ https://www.ncbi.nlm.nih.gov/pubmed/24160992 http://dx.doi.org/10.1186/1423-0127-20-81 |
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author | Kim, Sung-Eun Ko, Il-Gyu Hwang, Lakkyong Choi, In-Young Shin, Mal-Soon Kim, Chang-Ju Kim, Khae-Hawn |
author_facet | Kim, Sung-Eun Ko, Il-Gyu Hwang, Lakkyong Choi, In-Young Shin, Mal-Soon Kim, Chang-Ju Kim, Khae-Hawn |
author_sort | Kim, Sung-Eun |
collection | PubMed |
description | BACKGROUND: Tamsulosin, an α1-adrenoceptor antagonist, and sildenafil, a phosphodiesterase (PDE) inhibitor, are reported to improve lower urinary tract symptoms including overactive bladder (OAB). This study is aimed at investing the effects of tamsulosin and sildenafil and comparing the degree of the suppressive effects on the afferent pathways of micturition between them using an animal model of OAB, the spontaneously hypertensive rat (SHR). RESULTS: The cystometric parameters, the basal pressure and duration of bladder contraction, were significantly increased in the SHR group as compared with the Wistar-Kyoto (WKY) group. The intercontraction interval also significantly decreased in the SHR group. In the SHR-Tam 0.01 mg/kg group and the SHR-Sil 1 mg/kg group, however, the basal pressure and duration were significantly reduced and the intercontraction interval was significantly prolonged. Moreover, the degree of the expression of c-Fos and NGF was significantly higher in the SHR group as compared with the WKY group. But it was significantly reduced in the SHR-Tam 0.01 mg/kg group and the SHR-Sil 1 mg/kg group. Furthermore, tamsulosin had a higher degree of effect as compared with sildenafil. CONCLUSIONS: In conclusion, α1-adrenergic receptor antagonists and PDE-5 inhibitors may have an effect in improving the voiding functions through an inhibition of the neuronal activity in the afferent pathways of micturition. |
format | Online Article Text |
id | pubmed-3871018 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38710182013-12-25 An animal study to compare the degree of the suppressive effects on the afferent pathways of micturition between tamsulosin and sildenafil Kim, Sung-Eun Ko, Il-Gyu Hwang, Lakkyong Choi, In-Young Shin, Mal-Soon Kim, Chang-Ju Kim, Khae-Hawn J Biomed Sci Research BACKGROUND: Tamsulosin, an α1-adrenoceptor antagonist, and sildenafil, a phosphodiesterase (PDE) inhibitor, are reported to improve lower urinary tract symptoms including overactive bladder (OAB). This study is aimed at investing the effects of tamsulosin and sildenafil and comparing the degree of the suppressive effects on the afferent pathways of micturition between them using an animal model of OAB, the spontaneously hypertensive rat (SHR). RESULTS: The cystometric parameters, the basal pressure and duration of bladder contraction, were significantly increased in the SHR group as compared with the Wistar-Kyoto (WKY) group. The intercontraction interval also significantly decreased in the SHR group. In the SHR-Tam 0.01 mg/kg group and the SHR-Sil 1 mg/kg group, however, the basal pressure and duration were significantly reduced and the intercontraction interval was significantly prolonged. Moreover, the degree of the expression of c-Fos and NGF was significantly higher in the SHR group as compared with the WKY group. But it was significantly reduced in the SHR-Tam 0.01 mg/kg group and the SHR-Sil 1 mg/kg group. Furthermore, tamsulosin had a higher degree of effect as compared with sildenafil. CONCLUSIONS: In conclusion, α1-adrenergic receptor antagonists and PDE-5 inhibitors may have an effect in improving the voiding functions through an inhibition of the neuronal activity in the afferent pathways of micturition. BioMed Central 2013-10-25 /pmc/articles/PMC3871018/ /pubmed/24160992 http://dx.doi.org/10.1186/1423-0127-20-81 Text en Copyright © 2013 Kim et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Kim, Sung-Eun Ko, Il-Gyu Hwang, Lakkyong Choi, In-Young Shin, Mal-Soon Kim, Chang-Ju Kim, Khae-Hawn An animal study to compare the degree of the suppressive effects on the afferent pathways of micturition between tamsulosin and sildenafil |
title | An animal study to compare the degree of the suppressive effects on the afferent pathways of micturition between tamsulosin and sildenafil |
title_full | An animal study to compare the degree of the suppressive effects on the afferent pathways of micturition between tamsulosin and sildenafil |
title_fullStr | An animal study to compare the degree of the suppressive effects on the afferent pathways of micturition between tamsulosin and sildenafil |
title_full_unstemmed | An animal study to compare the degree of the suppressive effects on the afferent pathways of micturition between tamsulosin and sildenafil |
title_short | An animal study to compare the degree of the suppressive effects on the afferent pathways of micturition between tamsulosin and sildenafil |
title_sort | animal study to compare the degree of the suppressive effects on the afferent pathways of micturition between tamsulosin and sildenafil |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3871018/ https://www.ncbi.nlm.nih.gov/pubmed/24160992 http://dx.doi.org/10.1186/1423-0127-20-81 |
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