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The Potential of Asiatic Acid in the Reversion of Cyclophosphamide-Induced Hemorrhagic Cystitis in Rats

The purpose of this study was to determine if asiatic acid may act efficiently in the model of cyclophosphamide (CYP)-induced cystitis in rats. We performed experiments after administration of CYP (single dose 200 mg/kg, intraperitoneally), asiatic acid (30 mg/kg/day for 14 consecutive days, by oral...

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Autores principales: Wróbel, Andrzej, Zapała, Łukasz, Kluz, Tomasz, Rogowski, Artur, Misiek, Marcin, Juszczak, Kajetan, Sieńko, Jacek, Gold, Daniela, Stangel-Wójcikiewicz, Klaudia, Poleszak, Ewa, Radziszewski, Piotr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8198845/
https://www.ncbi.nlm.nih.gov/pubmed/34072606
http://dx.doi.org/10.3390/ijms22115853
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author Wróbel, Andrzej
Zapała, Łukasz
Kluz, Tomasz
Rogowski, Artur
Misiek, Marcin
Juszczak, Kajetan
Sieńko, Jacek
Gold, Daniela
Stangel-Wójcikiewicz, Klaudia
Poleszak, Ewa
Radziszewski, Piotr
author_facet Wróbel, Andrzej
Zapała, Łukasz
Kluz, Tomasz
Rogowski, Artur
Misiek, Marcin
Juszczak, Kajetan
Sieńko, Jacek
Gold, Daniela
Stangel-Wójcikiewicz, Klaudia
Poleszak, Ewa
Radziszewski, Piotr
author_sort Wróbel, Andrzej
collection PubMed
description The purpose of this study was to determine if asiatic acid may act efficiently in the model of cyclophosphamide (CYP)-induced cystitis in rats. We performed experiments after administration of CYP (single dose 200 mg/kg, intraperitoneally), asiatic acid (30 mg/kg/day for 14 consecutive days, by oral gavage), or CYP plus asiatic acid, during which conscious cystometry, measurements of urothelium thickness and bladder edema, as well as selected biomarkers analyses were conducted. In rats that received asiatic acid together with CYP, a drop in bladder basal pressure, detrusor overactivity index, non-voiding contraction amplitude, non-voiding contraction frequency, and the area under the pressure curve were observed, when compared to the CYP group. Furthermore, a significant increase in threshold pressure, voided volume, intercontraction interval, bladder compliance, and volume threshold to elicit NVC were found in that group accordingly. Administration of the asiatic acid successfully restored concentrations of biomarkers both in bladder urothelium (BDNF, CGRP, OCT-3, IL-1β, IL-6, NGF, nitrotyrosine, malondialdehyde, TNF-α, SV2A, SNAP23, SNAP25, PAC-1, ORM1, occludin, IGFBP-3, HB-EGF, T–H protein, Z01, and HPX) and detrusor muscle (Rho kinase and VAChT) in CYP-treated rats. Finally, asiatic acid significantly decreased urothelium thickness and bladder oedema. Asiatic acid proved to be a potent and effective drug in the rat model of CYP-induced cystitis.
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spelling pubmed-81988452021-06-14 The Potential of Asiatic Acid in the Reversion of Cyclophosphamide-Induced Hemorrhagic Cystitis in Rats Wróbel, Andrzej Zapała, Łukasz Kluz, Tomasz Rogowski, Artur Misiek, Marcin Juszczak, Kajetan Sieńko, Jacek Gold, Daniela Stangel-Wójcikiewicz, Klaudia Poleszak, Ewa Radziszewski, Piotr Int J Mol Sci Article The purpose of this study was to determine if asiatic acid may act efficiently in the model of cyclophosphamide (CYP)-induced cystitis in rats. We performed experiments after administration of CYP (single dose 200 mg/kg, intraperitoneally), asiatic acid (30 mg/kg/day for 14 consecutive days, by oral gavage), or CYP plus asiatic acid, during which conscious cystometry, measurements of urothelium thickness and bladder edema, as well as selected biomarkers analyses were conducted. In rats that received asiatic acid together with CYP, a drop in bladder basal pressure, detrusor overactivity index, non-voiding contraction amplitude, non-voiding contraction frequency, and the area under the pressure curve were observed, when compared to the CYP group. Furthermore, a significant increase in threshold pressure, voided volume, intercontraction interval, bladder compliance, and volume threshold to elicit NVC were found in that group accordingly. Administration of the asiatic acid successfully restored concentrations of biomarkers both in bladder urothelium (BDNF, CGRP, OCT-3, IL-1β, IL-6, NGF, nitrotyrosine, malondialdehyde, TNF-α, SV2A, SNAP23, SNAP25, PAC-1, ORM1, occludin, IGFBP-3, HB-EGF, T–H protein, Z01, and HPX) and detrusor muscle (Rho kinase and VAChT) in CYP-treated rats. Finally, asiatic acid significantly decreased urothelium thickness and bladder oedema. Asiatic acid proved to be a potent and effective drug in the rat model of CYP-induced cystitis. MDPI 2021-05-29 /pmc/articles/PMC8198845/ /pubmed/34072606 http://dx.doi.org/10.3390/ijms22115853 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wróbel, Andrzej
Zapała, Łukasz
Kluz, Tomasz
Rogowski, Artur
Misiek, Marcin
Juszczak, Kajetan
Sieńko, Jacek
Gold, Daniela
Stangel-Wójcikiewicz, Klaudia
Poleszak, Ewa
Radziszewski, Piotr
The Potential of Asiatic Acid in the Reversion of Cyclophosphamide-Induced Hemorrhagic Cystitis in Rats
title The Potential of Asiatic Acid in the Reversion of Cyclophosphamide-Induced Hemorrhagic Cystitis in Rats
title_full The Potential of Asiatic Acid in the Reversion of Cyclophosphamide-Induced Hemorrhagic Cystitis in Rats
title_fullStr The Potential of Asiatic Acid in the Reversion of Cyclophosphamide-Induced Hemorrhagic Cystitis in Rats
title_full_unstemmed The Potential of Asiatic Acid in the Reversion of Cyclophosphamide-Induced Hemorrhagic Cystitis in Rats
title_short The Potential of Asiatic Acid in the Reversion of Cyclophosphamide-Induced Hemorrhagic Cystitis in Rats
title_sort potential of asiatic acid in the reversion of cyclophosphamide-induced hemorrhagic cystitis in rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8198845/
https://www.ncbi.nlm.nih.gov/pubmed/34072606
http://dx.doi.org/10.3390/ijms22115853
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