The effects of tempol on cyclophosphamide-induced oxidative stress in rat micturition reflexes.

Published

Journal Article

We hypothesized that cyclophosphamide- (CYP-) induced cystitis results in oxidative stress and contributes to urinary bladder dysfunction. We determined (1) the expression of oxidative stress markers 3-nitrotyrosine (3-NT), reactive oxygen species (ROS)/reactive nitrogen species (RNS), inflammatory modulators, neuropeptides calcitonin gene-related peptide (CGRP), substance P (Sub P), and adenosine triphosphate (ATP) that contribute to the inflammatory process in the urinary tract and (2) the functional role of oxidative stress in urinary bladder dysfunction with an antioxidant, Tempol, (1 mM in drinking water) combined with conscious cystometry. In CYP-treated (4 hr or 48 hr; 150 mg/kg, i.p.) rats, ROS/RNS and 3-NT significantly (P ≤ 0.01) increased in urinary bladder. CYP treatment increased ATP, Sub P, and CGRP expression in the urinary bladder and cystometric fluid. In CYP-treated rats, Tempol significantly (P ≤ 0.01) increased bladder capacity and reduced voiding frequency compared to CYP-treated rats without Tempol. Tempol significantly (P ≤ 0.01) reduced ATP expression, 3-NT, and ROS/RNS expression in the urinary tract of CYP-treated rats. These studies demonstrate that reducing oxidative stress in CYP-induced cystitis improves urinary bladder function and reduces markers of oxidative stress and inflammation.

Full Text

Duke Authors

Cited Authors

  • Gonzalez, EJ; Peterson, A; Malley, S; Daniel, M; Lambert, D; Kosofsky, M; Vizzard, MA

Published Date

  • January 2015

Published In

Volume / Issue

  • 2015 /

Start / End Page

  • 545048 -

PubMed ID

  • 25973443

Pubmed Central ID

  • 25973443

Electronic International Standard Serial Number (EISSN)

  • 1537-744X

International Standard Serial Number (ISSN)

  • 2356-6140

Digital Object Identifier (DOI)

  • 10.1155/2015/545048

Language

  • eng