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High-definition ultrasound characterization of acute cyclophosphamide-induced cystitis in the mouse

PURPOSE: To examine associations if any between changes in voiding function, hematuria, and bladder ultrasonography metrics in murine cyclophosphamide-induced chemical cystitis. MATERIALS AND METHODS: Cystitis was induced in 6 female mice by an intraperitoneal injection of cyclophosphamide (300 mg/k...

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Autores principales: Lee, Toy G., Sanderson, Derrick, Doyle, Paula, Li, Dongmei, Wood, Ronald W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Urological Association 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6946820/
https://www.ncbi.nlm.nih.gov/pubmed/31942466
http://dx.doi.org/10.4111/icu.2020.61.1.75
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author Lee, Toy G.
Sanderson, Derrick
Doyle, Paula
Li, Dongmei
Wood, Ronald W.
author_facet Lee, Toy G.
Sanderson, Derrick
Doyle, Paula
Li, Dongmei
Wood, Ronald W.
author_sort Lee, Toy G.
collection PubMed
description PURPOSE: To examine associations if any between changes in voiding function, hematuria, and bladder ultrasonography metrics in murine cyclophosphamide-induced chemical cystitis. MATERIALS AND METHODS: Cystitis was induced in 6 female mice by an intraperitoneal injection of cyclophosphamide (300 mg/kg). Voiding frequency, void volume, hematuria assessment, and ultrasonographic measurements of the bladder were obtained at baseline, days 1 to 5, and days 9, 11, and 13. Voiding was induced with preferred sweet drinking solution and voiding data collected using an automated data collection system in 135 minute sessions. Bladder wall thickness, lumen volume, and vascular Doppler were acquired using a high definition ultrasound system. Spearman's correlation was used to analyze the association between the voiding changes, hematuria, and ultrasound findings. RESULTS: Hematuria was present 24 hours after cyclophosphamide injection. All animals displayed increased bladder vascularity, bladder wall thickness, and void frequency that was associated with concurrent decreased total and average void volumes. Increased bladder wall vascularity was correlated with the presence of hematuria (r=0.59, p<0.01) and bladder wall thickness (r=0.79, p<0.01). Hematuria correlated with increased void frequency (r=0.34, p<0.01). Average void volume was negatively correlated with hematuria (r=−0.50, p<0.01) and frequency (r=−0.38, p<0.01). CONCLUSIONS: High-definition ultrasound imaging permits in vivo monitoring of changes in bladder morphology associated with voiding function in relation to cyclophosphamide-induced cystitis. Ultrasound imaging of the bladder may assist in differential diagnosis of bladder dysfunction.
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spelling pubmed-69468202020-01-15 High-definition ultrasound characterization of acute cyclophosphamide-induced cystitis in the mouse Lee, Toy G. Sanderson, Derrick Doyle, Paula Li, Dongmei Wood, Ronald W. Investig Clin Urol Original Article PURPOSE: To examine associations if any between changes in voiding function, hematuria, and bladder ultrasonography metrics in murine cyclophosphamide-induced chemical cystitis. MATERIALS AND METHODS: Cystitis was induced in 6 female mice by an intraperitoneal injection of cyclophosphamide (300 mg/kg). Voiding frequency, void volume, hematuria assessment, and ultrasonographic measurements of the bladder were obtained at baseline, days 1 to 5, and days 9, 11, and 13. Voiding was induced with preferred sweet drinking solution and voiding data collected using an automated data collection system in 135 minute sessions. Bladder wall thickness, lumen volume, and vascular Doppler were acquired using a high definition ultrasound system. Spearman's correlation was used to analyze the association between the voiding changes, hematuria, and ultrasound findings. RESULTS: Hematuria was present 24 hours after cyclophosphamide injection. All animals displayed increased bladder vascularity, bladder wall thickness, and void frequency that was associated with concurrent decreased total and average void volumes. Increased bladder wall vascularity was correlated with the presence of hematuria (r=0.59, p<0.01) and bladder wall thickness (r=0.79, p<0.01). Hematuria correlated with increased void frequency (r=0.34, p<0.01). Average void volume was negatively correlated with hematuria (r=−0.50, p<0.01) and frequency (r=−0.38, p<0.01). CONCLUSIONS: High-definition ultrasound imaging permits in vivo monitoring of changes in bladder morphology associated with voiding function in relation to cyclophosphamide-induced cystitis. Ultrasound imaging of the bladder may assist in differential diagnosis of bladder dysfunction. The Korean Urological Association 2020-01 2019-12-04 /pmc/articles/PMC6946820/ /pubmed/31942466 http://dx.doi.org/10.4111/icu.2020.61.1.75 Text en © The Korean Urological Association, 2020 http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lee, Toy G.
Sanderson, Derrick
Doyle, Paula
Li, Dongmei
Wood, Ronald W.
High-definition ultrasound characterization of acute cyclophosphamide-induced cystitis in the mouse
title High-definition ultrasound characterization of acute cyclophosphamide-induced cystitis in the mouse
title_full High-definition ultrasound characterization of acute cyclophosphamide-induced cystitis in the mouse
title_fullStr High-definition ultrasound characterization of acute cyclophosphamide-induced cystitis in the mouse
title_full_unstemmed High-definition ultrasound characterization of acute cyclophosphamide-induced cystitis in the mouse
title_short High-definition ultrasound characterization of acute cyclophosphamide-induced cystitis in the mouse
title_sort high-definition ultrasound characterization of acute cyclophosphamide-induced cystitis in the mouse
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6946820/
https://www.ncbi.nlm.nih.gov/pubmed/31942466
http://dx.doi.org/10.4111/icu.2020.61.1.75
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