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Potentilla chinensis aqueous extract attenuates cyclophosphamide-induced hemorrhagic cystitis in rat model

Cyclophosphamide (CYP) damages all mucosal defence lines and induces hemorrhagic cystitis (HC) leading to detrusor overactivity. Patients who undergo combined chemio-radiotherapy are at higher risk of HC. Potentilla chinensis extract (PCE) prevent oxidative stress-dependent diseases. Thus, the aim o...

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Autores principales: Juszczak, Kajetan, Adamowicz, Jan, Zapała, Łukasz, Kluz, Tomasz, Adamczyk, Przemysław, Wdowiak, Artur, Bojar, Iwona, Misiek, Marcin, Grzybowska, Magdalena Emilia, Stangel-Wójcikiewicz, Klaudia, Poleszak, Ewa, Pokrywczyńska, Marta, Drewa, Tomasz, Wróbel, Andrzej
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9338276/
https://www.ncbi.nlm.nih.gov/pubmed/35906474
http://dx.doi.org/10.1038/s41598-022-17393-8
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author Juszczak, Kajetan
Adamowicz, Jan
Zapała, Łukasz
Kluz, Tomasz
Adamczyk, Przemysław
Wdowiak, Artur
Bojar, Iwona
Misiek, Marcin
Grzybowska, Magdalena Emilia
Stangel-Wójcikiewicz, Klaudia
Poleszak, Ewa
Pokrywczyńska, Marta
Drewa, Tomasz
Wróbel, Andrzej
author_facet Juszczak, Kajetan
Adamowicz, Jan
Zapała, Łukasz
Kluz, Tomasz
Adamczyk, Przemysław
Wdowiak, Artur
Bojar, Iwona
Misiek, Marcin
Grzybowska, Magdalena Emilia
Stangel-Wójcikiewicz, Klaudia
Poleszak, Ewa
Pokrywczyńska, Marta
Drewa, Tomasz
Wróbel, Andrzej
author_sort Juszczak, Kajetan
collection PubMed
description Cyclophosphamide (CYP) damages all mucosal defence lines and induces hemorrhagic cystitis (HC) leading to detrusor overactivity. Patients who undergo combined chemio-radiotherapy are at higher risk of HC. Potentilla chinensis extract (PCE) prevent oxidative stress-dependent diseases. Thus, the aim of the study was to investigate the effect of PCE on urinary bladder function in CYP-induced HC in preclinical study. 60 rats were divided into 4 groups, as follows: I—control, II—rats with CYP-induced HC, III—rats received PCE in dose of 500 mg/kg, and IV—rats with CYP-induced HC which received PCE in dose of 500 mg/kg. PCE or vehicle were administered orally for 14 days. The cystometry was performed 3 days after the last dose of the PCE. Next, urothelium thickness and oedema measurement and biochemical analyses were performed. Cyclophosphamide induced hemorrhagic cystitis. PCE had no influence on the urinary bladder function and micturition cycles in normal rats. PCE diminished the severity of CYP-induced hemorrhagic cystitis. In the urothelium the cyclophosphamide induced the elevation of CGRP, TNF-α, IL-6, IL-1β, OTC(3,) NIT, and MAL. Also, the level of T-H protein, HB-EGF, and ZO1 was decreased. Moreover, the level of ROCK1 and VAChT in detrusor muscle increased. cyclophosphamide caused an increased concentration of BDNF and NGF in the urine. In turn, PCE in cyclophosphamide-induced hemorrhagic cystitis caused a reversal of the described biochemical changes within urothelium, detrusor muscle and urine. PCE attenuates detrusor overactivity. In conclusion, our results revealed that PCE attenuates detrusor overactivity in case of cyclophosphamide-induced hemorrhagic cystitis. The potential properties of PCE appear to be important in terms of preventing of oxidative stress-dependent dysfunction of urinary bladder. PCE may become a potential supportive treatment in patient to whom cyclophosphamide-based chemotherapy is used.
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spelling pubmed-93382762022-07-31 Potentilla chinensis aqueous extract attenuates cyclophosphamide-induced hemorrhagic cystitis in rat model Juszczak, Kajetan Adamowicz, Jan Zapała, Łukasz Kluz, Tomasz Adamczyk, Przemysław Wdowiak, Artur Bojar, Iwona Misiek, Marcin Grzybowska, Magdalena Emilia Stangel-Wójcikiewicz, Klaudia Poleszak, Ewa Pokrywczyńska, Marta Drewa, Tomasz Wróbel, Andrzej Sci Rep Article Cyclophosphamide (CYP) damages all mucosal defence lines and induces hemorrhagic cystitis (HC) leading to detrusor overactivity. Patients who undergo combined chemio-radiotherapy are at higher risk of HC. Potentilla chinensis extract (PCE) prevent oxidative stress-dependent diseases. Thus, the aim of the study was to investigate the effect of PCE on urinary bladder function in CYP-induced HC in preclinical study. 60 rats were divided into 4 groups, as follows: I—control, II—rats with CYP-induced HC, III—rats received PCE in dose of 500 mg/kg, and IV—rats with CYP-induced HC which received PCE in dose of 500 mg/kg. PCE or vehicle were administered orally for 14 days. The cystometry was performed 3 days after the last dose of the PCE. Next, urothelium thickness and oedema measurement and biochemical analyses were performed. Cyclophosphamide induced hemorrhagic cystitis. PCE had no influence on the urinary bladder function and micturition cycles in normal rats. PCE diminished the severity of CYP-induced hemorrhagic cystitis. In the urothelium the cyclophosphamide induced the elevation of CGRP, TNF-α, IL-6, IL-1β, OTC(3,) NIT, and MAL. Also, the level of T-H protein, HB-EGF, and ZO1 was decreased. Moreover, the level of ROCK1 and VAChT in detrusor muscle increased. cyclophosphamide caused an increased concentration of BDNF and NGF in the urine. In turn, PCE in cyclophosphamide-induced hemorrhagic cystitis caused a reversal of the described biochemical changes within urothelium, detrusor muscle and urine. PCE attenuates detrusor overactivity. In conclusion, our results revealed that PCE attenuates detrusor overactivity in case of cyclophosphamide-induced hemorrhagic cystitis. The potential properties of PCE appear to be important in terms of preventing of oxidative stress-dependent dysfunction of urinary bladder. PCE may become a potential supportive treatment in patient to whom cyclophosphamide-based chemotherapy is used. Nature Publishing Group UK 2022-07-29 /pmc/articles/PMC9338276/ /pubmed/35906474 http://dx.doi.org/10.1038/s41598-022-17393-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Juszczak, Kajetan
Adamowicz, Jan
Zapała, Łukasz
Kluz, Tomasz
Adamczyk, Przemysław
Wdowiak, Artur
Bojar, Iwona
Misiek, Marcin
Grzybowska, Magdalena Emilia
Stangel-Wójcikiewicz, Klaudia
Poleszak, Ewa
Pokrywczyńska, Marta
Drewa, Tomasz
Wróbel, Andrzej
Potentilla chinensis aqueous extract attenuates cyclophosphamide-induced hemorrhagic cystitis in rat model
title Potentilla chinensis aqueous extract attenuates cyclophosphamide-induced hemorrhagic cystitis in rat model
title_full Potentilla chinensis aqueous extract attenuates cyclophosphamide-induced hemorrhagic cystitis in rat model
title_fullStr Potentilla chinensis aqueous extract attenuates cyclophosphamide-induced hemorrhagic cystitis in rat model
title_full_unstemmed Potentilla chinensis aqueous extract attenuates cyclophosphamide-induced hemorrhagic cystitis in rat model
title_short Potentilla chinensis aqueous extract attenuates cyclophosphamide-induced hemorrhagic cystitis in rat model
title_sort potentilla chinensis aqueous extract attenuates cyclophosphamide-induced hemorrhagic cystitis in rat model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9338276/
https://www.ncbi.nlm.nih.gov/pubmed/35906474
http://dx.doi.org/10.1038/s41598-022-17393-8
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