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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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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. |
format | Online Article Text |
id | pubmed-8198845 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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