Low concentrations of niflumic acid enhance basal spontaneous and carbachol-induced contractions of the detrusor

Purpose The urinary bladder expresses Ca 2+ -activated Cl − channels (CACC), but its physiological role in governing contractility remains to be defined. The CACC modulator niflumic acid (NFA) is widely used despite the variable results arisen from different drug concentrations used. This study was...

Full description

Saved in:
Bibliographic Details
Published inInternational urology and nephrology Vol. 46; no. 2; pp. 349 - 357
Main Authors Lam, Wai Ping, Tang, Hong Chai, Zhang, Xin, Leung, Ping Chung, Yew, David Tai Wai, Liang, Willmann
Format Journal Article
LanguageEnglish
Published Dordrecht Springer Netherlands 01.02.2014
Springer Nature B.V
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Purpose The urinary bladder expresses Ca 2+ -activated Cl − channels (CACC), but its physiological role in governing contractility remains to be defined. The CACC modulator niflumic acid (NFA) is widely used despite the variable results arisen from different drug concentrations used. This study was designed to examine the effects of NFA at low concentrations on detrusor strip contractility. Methods Rat detrusor strips with mucosa-intact (+MU) and mucosa-denuded (−MU) were prepared in transverse (Tr) and longitudinal (Lg) with respect to the bladder orientation. Isometric force measurements were made at baseline (for spontaneous phasic contractile activity) and during drug stimulation (by carbachol, CCh) with and without NFA. Results NFA (1 and 10 μmol/L) pretreatment enhanced CCh-induced contractions more in +MU than −MU strips with no selectivity on contractile direction. For spontaneous phasic contractions, NFA-treated strips in the Tr direction showed increased phasic amplitude, while phasic frequency was unchanged. Conclusions The findings suggest low concentrations of NFA having a potentiating effect on detrusor contractions that was sensitive to the MU and contractile direction.
ISSN:0301-1623
1573-2584
DOI:10.1007/s11255-013-0550-8