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Effects of nitric oxide inhibitors in mice with bladder outlet obstruction
PURPOSE: To investigate the lower urinary tract changes in mice treated with L-NAME, a non-selective competitive inhibitor of nitric oxide synthase (NOS), or aminoguanidine, a competitive inhibitor of inducible nitric oxide synthase (iNOS), after 5 weeks of partial bladder outlet obstruction (BOO),...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Urologia
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5433376/ https://www.ncbi.nlm.nih.gov/pubmed/28328190 http://dx.doi.org/10.1590/S1677-5538.IBJU.2015.0441 |
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author | Pereira, Marcy Lancia D’ancona, Carlos Arturo Levi Rojas-Moscoso, Julio Alejandro Ramos, Antonio Celso Saragossa Mónica, Fabiola Zakia Antunes, Edson |
author_facet | Pereira, Marcy Lancia D’ancona, Carlos Arturo Levi Rojas-Moscoso, Julio Alejandro Ramos, Antonio Celso Saragossa Mónica, Fabiola Zakia Antunes, Edson |
author_sort | Pereira, Marcy Lancia |
collection | PubMed |
description | PURPOSE: To investigate the lower urinary tract changes in mice treated with L-NAME, a non-selective competitive inhibitor of nitric oxide synthase (NOS), or aminoguanidine, a competitive inhibitor of inducible nitric oxide synthase (iNOS), after 5 weeks of partial bladder outlet obstruction (BOO), in order to evaluate the role of constitutive and non-constitutive NOS in the pathogenesis of this experimental condition. MATERIALS AND METHODS: C57BL6 male mice were partially obstructed and randomly allocated into 6 groups: Sham, Sham + L-NAME, Sham + aminoguanidine, BOO, BOO + L-NAME and BOO + aminoguanidine. After 5 weeks, bladder weight was obtained and cystometry and tissue bath contractile studies were performed. RESULTS: BOO animals showed increase of non-voiding contractions (NVC) and bladder capacity, and also less contractile response to Carbachol and Electric Field Stimulation. Inhibition of NOS isoforms improved bladder capacity and compliance in BOO animals. L-NAME caused more NVC, prevented bladder weight gain and leaded to augmented contractile responses at muscarinic and electric stimulation. Aminoguanidine diminished NVC, but did not avoid bladder weight gain in BOO animals and did not improve contractile responses. CONCLUSION: It can be hypothesized that chronic inhibition of three NOS isoforms in BOO animals leaded to worsening of bladder function, while selective inhibition of iNOS did not improve responses, what suggests that, in BOO animals, alterations are related to constitutive NOS. |
format | Online Article Text |
id | pubmed-5433376 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Sociedade Brasileira de Urologia |
record_format | MEDLINE/PubMed |
spelling | pubmed-54333762017-05-30 Effects of nitric oxide inhibitors in mice with bladder outlet obstruction Pereira, Marcy Lancia D’ancona, Carlos Arturo Levi Rojas-Moscoso, Julio Alejandro Ramos, Antonio Celso Saragossa Mónica, Fabiola Zakia Antunes, Edson Int Braz J Urol Original Article PURPOSE: To investigate the lower urinary tract changes in mice treated with L-NAME, a non-selective competitive inhibitor of nitric oxide synthase (NOS), or aminoguanidine, a competitive inhibitor of inducible nitric oxide synthase (iNOS), after 5 weeks of partial bladder outlet obstruction (BOO), in order to evaluate the role of constitutive and non-constitutive NOS in the pathogenesis of this experimental condition. MATERIALS AND METHODS: C57BL6 male mice were partially obstructed and randomly allocated into 6 groups: Sham, Sham + L-NAME, Sham + aminoguanidine, BOO, BOO + L-NAME and BOO + aminoguanidine. After 5 weeks, bladder weight was obtained and cystometry and tissue bath contractile studies were performed. RESULTS: BOO animals showed increase of non-voiding contractions (NVC) and bladder capacity, and also less contractile response to Carbachol and Electric Field Stimulation. Inhibition of NOS isoforms improved bladder capacity and compliance in BOO animals. L-NAME caused more NVC, prevented bladder weight gain and leaded to augmented contractile responses at muscarinic and electric stimulation. Aminoguanidine diminished NVC, but did not avoid bladder weight gain in BOO animals and did not improve contractile responses. CONCLUSION: It can be hypothesized that chronic inhibition of three NOS isoforms in BOO animals leaded to worsening of bladder function, while selective inhibition of iNOS did not improve responses, what suggests that, in BOO animals, alterations are related to constitutive NOS. Sociedade Brasileira de Urologia 2017 /pmc/articles/PMC5433376/ /pubmed/28328190 http://dx.doi.org/10.1590/S1677-5538.IBJU.2015.0441 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Pereira, Marcy Lancia D’ancona, Carlos Arturo Levi Rojas-Moscoso, Julio Alejandro Ramos, Antonio Celso Saragossa Mónica, Fabiola Zakia Antunes, Edson Effects of nitric oxide inhibitors in mice with bladder outlet obstruction |
title | Effects of nitric oxide inhibitors in mice with bladder outlet obstruction |
title_full | Effects of nitric oxide inhibitors in mice with bladder outlet obstruction |
title_fullStr | Effects of nitric oxide inhibitors in mice with bladder outlet obstruction |
title_full_unstemmed | Effects of nitric oxide inhibitors in mice with bladder outlet obstruction |
title_short | Effects of nitric oxide inhibitors in mice with bladder outlet obstruction |
title_sort | effects of nitric oxide inhibitors in mice with bladder outlet obstruction |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5433376/ https://www.ncbi.nlm.nih.gov/pubmed/28328190 http://dx.doi.org/10.1590/S1677-5538.IBJU.2015.0441 |
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