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Chemical cystitis developed in experimental animals model: Topical effect of intravesical ozone application to bladder
AIMS: To demonstrate the effects of intravesical ozone treatment on inflammation and epithelial cell damage in chemical cystitis animal model. MATERIALS AND METHODS: A total of 30 New Zealand rabbits were divided into six groups. Cystitis was conducted with transurethral intravesical hydrochloric ac...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4021650/ https://www.ncbi.nlm.nih.gov/pubmed/24833822 http://dx.doi.org/10.4103/0974-7796.130553 |
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author | Bayrak, Omer Erturhan, Sakip Seckiner, Ilker Erbagci, Ahmet Ustun, Abdulkerim Karakok, Metin |
author_facet | Bayrak, Omer Erturhan, Sakip Seckiner, Ilker Erbagci, Ahmet Ustun, Abdulkerim Karakok, Metin |
author_sort | Bayrak, Omer |
collection | PubMed |
description | AIMS: To demonstrate the effects of intravesical ozone treatment on inflammation and epithelial cell damage in chemical cystitis animal model. MATERIALS AND METHODS: A total of 30 New Zealand rabbits were divided into six groups. Cystitis was conducted with transurethral intravesical hydrochloric acid instillation on the subjects in Groups IA, IB, IIA, and IIB. Then, Group IA-IB subjects were transurethrally administered intravesical ozone therapy twice a week, while Group IIA-IIB subjects were only given intravesical isotonic NaCl instillation. Group IIIA-IIIB subjects were administered intravesical isotonic NaCl instillation without conducting chemical cystitis in order to create the same stress. Treatment schemes of all groups were arranged in the same manner. Following a 3-week (early period) and 6-week (late period) therapy, the rabbits were sacrificed and histopathologic investigations were carried out in order to demonstrate changes in the urinary bladder. RESULTS: In our study, we observed that the basal membrane and mucosal integrity were maintained, inflammatory cells were suppressed in Group IA-IB (Early and late period), which received ozone therapy. However, it was also observed that mucosal integrity was spoiled, numerous inflammatory cells were accumulated in Group IIA-IIB, which was administered isotonic NaCl. CONCLUSION: Due to its low cost and minimal side effects; ozone therapy could be a new therapeutic approach in the treatment of interstitial cystitis. |
format | Online Article Text |
id | pubmed-4021650 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-40216502014-05-15 Chemical cystitis developed in experimental animals model: Topical effect of intravesical ozone application to bladder Bayrak, Omer Erturhan, Sakip Seckiner, Ilker Erbagci, Ahmet Ustun, Abdulkerim Karakok, Metin Urol Ann Original Article AIMS: To demonstrate the effects of intravesical ozone treatment on inflammation and epithelial cell damage in chemical cystitis animal model. MATERIALS AND METHODS: A total of 30 New Zealand rabbits were divided into six groups. Cystitis was conducted with transurethral intravesical hydrochloric acid instillation on the subjects in Groups IA, IB, IIA, and IIB. Then, Group IA-IB subjects were transurethrally administered intravesical ozone therapy twice a week, while Group IIA-IIB subjects were only given intravesical isotonic NaCl instillation. Group IIIA-IIIB subjects were administered intravesical isotonic NaCl instillation without conducting chemical cystitis in order to create the same stress. Treatment schemes of all groups were arranged in the same manner. Following a 3-week (early period) and 6-week (late period) therapy, the rabbits were sacrificed and histopathologic investigations were carried out in order to demonstrate changes in the urinary bladder. RESULTS: In our study, we observed that the basal membrane and mucosal integrity were maintained, inflammatory cells were suppressed in Group IA-IB (Early and late period), which received ozone therapy. However, it was also observed that mucosal integrity was spoiled, numerous inflammatory cells were accumulated in Group IIA-IIB, which was administered isotonic NaCl. CONCLUSION: Due to its low cost and minimal side effects; ozone therapy could be a new therapeutic approach in the treatment of interstitial cystitis. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4021650/ /pubmed/24833822 http://dx.doi.org/10.4103/0974-7796.130553 Text en Copyright: © Urology Annals http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Bayrak, Omer Erturhan, Sakip Seckiner, Ilker Erbagci, Ahmet Ustun, Abdulkerim Karakok, Metin Chemical cystitis developed in experimental animals model: Topical effect of intravesical ozone application to bladder |
title | Chemical cystitis developed in experimental animals model: Topical effect of intravesical ozone application to bladder |
title_full | Chemical cystitis developed in experimental animals model: Topical effect of intravesical ozone application to bladder |
title_fullStr | Chemical cystitis developed in experimental animals model: Topical effect of intravesical ozone application to bladder |
title_full_unstemmed | Chemical cystitis developed in experimental animals model: Topical effect of intravesical ozone application to bladder |
title_short | Chemical cystitis developed in experimental animals model: Topical effect of intravesical ozone application to bladder |
title_sort | chemical cystitis developed in experimental animals model: topical effect of intravesical ozone application to bladder |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4021650/ https://www.ncbi.nlm.nih.gov/pubmed/24833822 http://dx.doi.org/10.4103/0974-7796.130553 |
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