Cargando…

Inflammation and enhanced nociceptive responses to bladder distension produced by intravesical zymosan in the rat

BACKGROUND: Mycotic infections of the bladder produce pain and inflammatory changes. The present study examined the inflammatory and nociceptive effects of the yeast cell wall component, zymosan, when admininstered into the urinary bladder in order to characterize this form of bladder sensitization....

Descripción completa

Detalles Bibliográficos
Autores principales: Randich, Alan, Uzzell, Tyler, Cannon, Ronda, Ness, Timothy J
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1395324/
https://www.ncbi.nlm.nih.gov/pubmed/16469099
http://dx.doi.org/10.1186/1471-2490-6-2
_version_ 1782126947176808448
author Randich, Alan
Uzzell, Tyler
Cannon, Ronda
Ness, Timothy J
author_facet Randich, Alan
Uzzell, Tyler
Cannon, Ronda
Ness, Timothy J
author_sort Randich, Alan
collection PubMed
description BACKGROUND: Mycotic infections of the bladder produce pain and inflammatory changes. The present study examined the inflammatory and nociceptive effects of the yeast cell wall component, zymosan, when admininstered into the urinary bladder in order to characterize this form of bladder sensitization. METHODS: Parametric analyses of the time-course (0–48 hr) and concentration (0–2% solutions) variables associated with intravesical zymosan-induced bladder inflammation were performed in female rats. Plasma extravasation of Evan's Blue dye was used as a measure of tissue inflammation. Cardiovascular and visceromotor responses to urinary bladder distension were used as measures of nociception. RESULTS: Zymosan-induced bladder inflammation, as indexed by plasma extravasation of Evan's Blue, was significantly greater in rats treated with either 1 or 2% solutions as compared to either 0.1 or 0.5% zymosan solutions. In time-course studies (1 – 48 hr post-treatment), 1% zymosan-induced inflammation progressively increased with time following administration, was greatest at 24 hr and began to normalize by 48 hr. In the studies of inflammation-induced changes in nociception, arterial blood pressure (ABP) and visceromotor responses to graded distension of the urinary bladder were significantly increased relative to controls 24 hr after zymosan administration. CONCLUSION: These studies provide important time-course and solution concentration parameters for studies of zymosan-induced inflammation of the bladder and suggest utility of this model for the study of bladder-related pain.
format Text
id pubmed-1395324
institution National Center for Biotechnology Information
language English
publishDate 2006
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-13953242006-03-09 Inflammation and enhanced nociceptive responses to bladder distension produced by intravesical zymosan in the rat Randich, Alan Uzzell, Tyler Cannon, Ronda Ness, Timothy J BMC Urol Research Article BACKGROUND: Mycotic infections of the bladder produce pain and inflammatory changes. The present study examined the inflammatory and nociceptive effects of the yeast cell wall component, zymosan, when admininstered into the urinary bladder in order to characterize this form of bladder sensitization. METHODS: Parametric analyses of the time-course (0–48 hr) and concentration (0–2% solutions) variables associated with intravesical zymosan-induced bladder inflammation were performed in female rats. Plasma extravasation of Evan's Blue dye was used as a measure of tissue inflammation. Cardiovascular and visceromotor responses to urinary bladder distension were used as measures of nociception. RESULTS: Zymosan-induced bladder inflammation, as indexed by plasma extravasation of Evan's Blue, was significantly greater in rats treated with either 1 or 2% solutions as compared to either 0.1 or 0.5% zymosan solutions. In time-course studies (1 – 48 hr post-treatment), 1% zymosan-induced inflammation progressively increased with time following administration, was greatest at 24 hr and began to normalize by 48 hr. In the studies of inflammation-induced changes in nociception, arterial blood pressure (ABP) and visceromotor responses to graded distension of the urinary bladder were significantly increased relative to controls 24 hr after zymosan administration. CONCLUSION: These studies provide important time-course and solution concentration parameters for studies of zymosan-induced inflammation of the bladder and suggest utility of this model for the study of bladder-related pain. BioMed Central 2006-02-09 /pmc/articles/PMC1395324/ /pubmed/16469099 http://dx.doi.org/10.1186/1471-2490-6-2 Text en Copyright © 2006 Randich et al; licensee BioMed Central Ltd.
spellingShingle Research Article
Randich, Alan
Uzzell, Tyler
Cannon, Ronda
Ness, Timothy J
Inflammation and enhanced nociceptive responses to bladder distension produced by intravesical zymosan in the rat
title Inflammation and enhanced nociceptive responses to bladder distension produced by intravesical zymosan in the rat
title_full Inflammation and enhanced nociceptive responses to bladder distension produced by intravesical zymosan in the rat
title_fullStr Inflammation and enhanced nociceptive responses to bladder distension produced by intravesical zymosan in the rat
title_full_unstemmed Inflammation and enhanced nociceptive responses to bladder distension produced by intravesical zymosan in the rat
title_short Inflammation and enhanced nociceptive responses to bladder distension produced by intravesical zymosan in the rat
title_sort inflammation and enhanced nociceptive responses to bladder distension produced by intravesical zymosan in the rat
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1395324/
https://www.ncbi.nlm.nih.gov/pubmed/16469099
http://dx.doi.org/10.1186/1471-2490-6-2
work_keys_str_mv AT randichalan inflammationandenhancednociceptiveresponsestobladderdistensionproducedbyintravesicalzymosanintherat
AT uzzelltyler inflammationandenhancednociceptiveresponsestobladderdistensionproducedbyintravesicalzymosanintherat
AT cannonronda inflammationandenhancednociceptiveresponsestobladderdistensionproducedbyintravesicalzymosanintherat
AT nesstimothyj inflammationandenhancednociceptiveresponsestobladderdistensionproducedbyintravesicalzymosanintherat