Dual involvements of cyclooxygenase and nitric oxide synthase expressions in ketamine-induced ulcerative cystitis in rat bladder

Shu Mien Chuang, Keh Min Liu, Yi Lun Li, Mei Yu Jang, Hei Hwa Lee, Wen Jeng Wu, Wei Chiao Chang, Robert M. Levin, Yung Shun Juan

Research output: Contribution to journalArticle

45 Citations (Scopus)

Abstract

Aims The aims of the present study were to investigate voiding patterns, tissue constituents and the expressions of cyclooxygenase-2 (COX-2) and nitric oxide synthase (NOS) involved in ketamine-induced ulcerative cystitis in rat urinary bladder. Methods Thirty Sprague-Dawley rats were distributed into three groups which received saline or ketamine (25 mg/kg/day) for a period of 14 and 28 days. In each group, cystometry was performed weekly and the concentration of ketamine and its metabolites (norketamine) was assayed. Paraffin-embedded sections were stained with Masson's trichrome stain, and ketamine-induced morphological changes were examined. Western blot analyses were carried out to examine the expressions of COX-2 and different NOS isoforms in bladder tissues. Immunofluorescence study was done to evaluate the expressions of COX-2 and macrophage infiltration (stained with ED-1 macrophage cell surface antigen) within the bladder. Results Ketamine treatment resulted in bladder hyperactivity and the non-voiding contractions were significantly increased. The urine concentrations of ketamine and norketamine were much higher in ketamine-treated group. Moreover, ulcerated urothelium and mononuclear cell infiltration were noted in ketamine-treated group. These alterations in urodynamic functions and tissue constituents were accompanied by increases in the expression of COX-2. Two NOS isoforms (iNOS and eNOS) were also overexpressed, but no significant change was observed for nNOS. COX-2 positive stained cells were significantly increased. Meanwhile, increased amounts of ED-1 positive stained macrophages were present and most of COX-2 expressed cells were co-stained with ED-1 in the early stage of ketamine treatment. Conclusions Ketamine treatment affected bladder tissues by enhancing interstitial fibrosis and accelerating macrophages infiltration. Ketamine also initiated the up-regulations of COX-2 and iNOS and eNOS expressions. These up-regulated enzymes might play an important role in contributing to ketamine-induced alterations in micturition patterns and ulcerative cystitis.

Original languageEnglish
Pages (from-to)1137-1143
Number of pages7
JournalNeurourology and Urodynamics
Volume32
Issue number8
DOIs
Publication statusPublished - Nov 2013

Fingerprint

Cystitis
Ketamine
Prostaglandin-Endoperoxide Synthases
Nitric Oxide Synthase
Urinary Bladder
Cyclooxygenase 2
Macrophages
Protein Isoforms
Urothelium
Urination
Urodynamics
Surface Antigens
Paraffin
Fluorescent Antibody Technique
Sprague Dawley Rats
Fibrosis
Up-Regulation
Therapeutics
Western Blotting
Urine

Keywords

  • cyclooxygenase-2
  • ketamine
  • nitric oxide synthase
  • ulcerative cystitis

ASJC Scopus subject areas

  • Clinical Neurology
  • Urology

Cite this

Dual involvements of cyclooxygenase and nitric oxide synthase expressions in ketamine-induced ulcerative cystitis in rat bladder. / Chuang, Shu Mien; Liu, Keh Min; Li, Yi Lun; Jang, Mei Yu; Lee, Hei Hwa; Wu, Wen Jeng; Chang, Wei Chiao; Levin, Robert M.; Juan, Yung Shun.

In: Neurourology and Urodynamics, Vol. 32, No. 8, 11.2013, p. 1137-1143.

Research output: Contribution to journalArticle

Chuang, Shu Mien ; Liu, Keh Min ; Li, Yi Lun ; Jang, Mei Yu ; Lee, Hei Hwa ; Wu, Wen Jeng ; Chang, Wei Chiao ; Levin, Robert M. ; Juan, Yung Shun. / Dual involvements of cyclooxygenase and nitric oxide synthase expressions in ketamine-induced ulcerative cystitis in rat bladder. In: Neurourology and Urodynamics. 2013 ; Vol. 32, No. 8. pp. 1137-1143.
@article{a6361941f8e54dac8d4a5da6b38d7450,
title = "Dual involvements of cyclooxygenase and nitric oxide synthase expressions in ketamine-induced ulcerative cystitis in rat bladder",
abstract = "Aims The aims of the present study were to investigate voiding patterns, tissue constituents and the expressions of cyclooxygenase-2 (COX-2) and nitric oxide synthase (NOS) involved in ketamine-induced ulcerative cystitis in rat urinary bladder. Methods Thirty Sprague-Dawley rats were distributed into three groups which received saline or ketamine (25 mg/kg/day) for a period of 14 and 28 days. In each group, cystometry was performed weekly and the concentration of ketamine and its metabolites (norketamine) was assayed. Paraffin-embedded sections were stained with Masson's trichrome stain, and ketamine-induced morphological changes were examined. Western blot analyses were carried out to examine the expressions of COX-2 and different NOS isoforms in bladder tissues. Immunofluorescence study was done to evaluate the expressions of COX-2 and macrophage infiltration (stained with ED-1 macrophage cell surface antigen) within the bladder. Results Ketamine treatment resulted in bladder hyperactivity and the non-voiding contractions were significantly increased. The urine concentrations of ketamine and norketamine were much higher in ketamine-treated group. Moreover, ulcerated urothelium and mononuclear cell infiltration were noted in ketamine-treated group. These alterations in urodynamic functions and tissue constituents were accompanied by increases in the expression of COX-2. Two NOS isoforms (iNOS and eNOS) were also overexpressed, but no significant change was observed for nNOS. COX-2 positive stained cells were significantly increased. Meanwhile, increased amounts of ED-1 positive stained macrophages were present and most of COX-2 expressed cells were co-stained with ED-1 in the early stage of ketamine treatment. Conclusions Ketamine treatment affected bladder tissues by enhancing interstitial fibrosis and accelerating macrophages infiltration. Ketamine also initiated the up-regulations of COX-2 and iNOS and eNOS expressions. These up-regulated enzymes might play an important role in contributing to ketamine-induced alterations in micturition patterns and ulcerative cystitis.",
keywords = "cyclooxygenase-2, ketamine, nitric oxide synthase, ulcerative cystitis",
author = "Chuang, {Shu Mien} and Liu, {Keh Min} and Li, {Yi Lun} and Jang, {Mei Yu} and Lee, {Hei Hwa} and Wu, {Wen Jeng} and Chang, {Wei Chiao} and Levin, {Robert M.} and Juan, {Yung Shun}",
year = "2013",
month = "11",
doi = "10.1002/nau.22367",
language = "English",
volume = "32",
pages = "1137--1143",
journal = "Neurourology and Urodynamics",
issn = "0733-2467",
publisher = "Wiley-Liss Inc.",
number = "8",

}

TY - JOUR

T1 - Dual involvements of cyclooxygenase and nitric oxide synthase expressions in ketamine-induced ulcerative cystitis in rat bladder

AU - Chuang, Shu Mien

AU - Liu, Keh Min

AU - Li, Yi Lun

AU - Jang, Mei Yu

AU - Lee, Hei Hwa

AU - Wu, Wen Jeng

AU - Chang, Wei Chiao

AU - Levin, Robert M.

AU - Juan, Yung Shun

PY - 2013/11

Y1 - 2013/11

N2 - Aims The aims of the present study were to investigate voiding patterns, tissue constituents and the expressions of cyclooxygenase-2 (COX-2) and nitric oxide synthase (NOS) involved in ketamine-induced ulcerative cystitis in rat urinary bladder. Methods Thirty Sprague-Dawley rats were distributed into three groups which received saline or ketamine (25 mg/kg/day) for a period of 14 and 28 days. In each group, cystometry was performed weekly and the concentration of ketamine and its metabolites (norketamine) was assayed. Paraffin-embedded sections were stained with Masson's trichrome stain, and ketamine-induced morphological changes were examined. Western blot analyses were carried out to examine the expressions of COX-2 and different NOS isoforms in bladder tissues. Immunofluorescence study was done to evaluate the expressions of COX-2 and macrophage infiltration (stained with ED-1 macrophage cell surface antigen) within the bladder. Results Ketamine treatment resulted in bladder hyperactivity and the non-voiding contractions were significantly increased. The urine concentrations of ketamine and norketamine were much higher in ketamine-treated group. Moreover, ulcerated urothelium and mononuclear cell infiltration were noted in ketamine-treated group. These alterations in urodynamic functions and tissue constituents were accompanied by increases in the expression of COX-2. Two NOS isoforms (iNOS and eNOS) were also overexpressed, but no significant change was observed for nNOS. COX-2 positive stained cells were significantly increased. Meanwhile, increased amounts of ED-1 positive stained macrophages were present and most of COX-2 expressed cells were co-stained with ED-1 in the early stage of ketamine treatment. Conclusions Ketamine treatment affected bladder tissues by enhancing interstitial fibrosis and accelerating macrophages infiltration. Ketamine also initiated the up-regulations of COX-2 and iNOS and eNOS expressions. These up-regulated enzymes might play an important role in contributing to ketamine-induced alterations in micturition patterns and ulcerative cystitis.

AB - Aims The aims of the present study were to investigate voiding patterns, tissue constituents and the expressions of cyclooxygenase-2 (COX-2) and nitric oxide synthase (NOS) involved in ketamine-induced ulcerative cystitis in rat urinary bladder. Methods Thirty Sprague-Dawley rats were distributed into three groups which received saline or ketamine (25 mg/kg/day) for a period of 14 and 28 days. In each group, cystometry was performed weekly and the concentration of ketamine and its metabolites (norketamine) was assayed. Paraffin-embedded sections were stained with Masson's trichrome stain, and ketamine-induced morphological changes were examined. Western blot analyses were carried out to examine the expressions of COX-2 and different NOS isoforms in bladder tissues. Immunofluorescence study was done to evaluate the expressions of COX-2 and macrophage infiltration (stained with ED-1 macrophage cell surface antigen) within the bladder. Results Ketamine treatment resulted in bladder hyperactivity and the non-voiding contractions were significantly increased. The urine concentrations of ketamine and norketamine were much higher in ketamine-treated group. Moreover, ulcerated urothelium and mononuclear cell infiltration were noted in ketamine-treated group. These alterations in urodynamic functions and tissue constituents were accompanied by increases in the expression of COX-2. Two NOS isoforms (iNOS and eNOS) were also overexpressed, but no significant change was observed for nNOS. COX-2 positive stained cells were significantly increased. Meanwhile, increased amounts of ED-1 positive stained macrophages were present and most of COX-2 expressed cells were co-stained with ED-1 in the early stage of ketamine treatment. Conclusions Ketamine treatment affected bladder tissues by enhancing interstitial fibrosis and accelerating macrophages infiltration. Ketamine also initiated the up-regulations of COX-2 and iNOS and eNOS expressions. These up-regulated enzymes might play an important role in contributing to ketamine-induced alterations in micturition patterns and ulcerative cystitis.

KW - cyclooxygenase-2

KW - ketamine

KW - nitric oxide synthase

KW - ulcerative cystitis

UR - http://www.scopus.com/inward/record.url?scp=84886444200&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84886444200&partnerID=8YFLogxK

U2 - 10.1002/nau.22367

DO - 10.1002/nau.22367

M3 - Article

C2 - 23359243

AN - SCOPUS:84886444200

VL - 32

SP - 1137

EP - 1143

JO - Neurourology and Urodynamics

JF - Neurourology and Urodynamics

SN - 0733-2467

IS - 8

ER -