β3-Adrenoceptor-mediated relaxation of rat and human urinary bladder: roles of BKCa channels and Rho kinase

Naunyn Schmiedebergs Arch Pharmacol. 2015 Jul;388(7):749-59. doi: 10.1007/s00210-015-1128-z. Epub 2015 May 9.

Abstract

Previous studies suggest that the large-conductance Ca(2+)-activated K(+) (BKCa) channel and Rho-kinase play major roles in the control of urinary bladder tone. Here, we investigated their involvement in β-adrenoceptor (AR)-mediated relaxation of rat and human bladder. Concentration-response curves of isoprenaline and mirabegron-induced bladder relaxation were generated against passive tension and KCl- and carbachol-induced tone, in the absence or presence of the BKCa channel inhibitor iberiotoxin (100 nM) or the Rho-kinase inhibitor Y27,632 (1 μM). Myosin light chain (MLC) phosphorylation was studied by Western blot. In rat, iberiotoxin only slightly altered isoprenaline- and mirabegron-induced relaxation against KCl-induced tone but attenuated relaxation by both agonists against carbachol-induced tone. Y27,632 enhanced isoprenaline- or mirabegron-induced relaxation only against carbachol-induced tone. In humans, iberiotoxin slightly enhanced relaxation by both agonists against carbachol-induced pre-contraction. Y27,632 did not change isoprenaline-induced relaxation but enhanced that by mirabegron. Under passive tension, MLC phosphorylation was markedly reduced by both β-AR agonists, an effect insensitive to Y27,632. In the presence of carbachol, both β-AR agonists increased MLC phosphorylation, an effect reduced by Y27,632 only in the presence of 1 μM carbachol. These results indicate that the extent of BKCa channel and Rho-kinase involvement in relaxation induced by β-AR agonists depends on pre contractile stimulus and species.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetanilides / pharmacology
  • Adrenergic beta-3 Receptor Agonists / pharmacology
  • Adult
  • Aged
  • Amides / pharmacology
  • Animals
  • Female
  • Humans
  • In Vitro Techniques
  • Large-Conductance Calcium-Activated Potassium Channel alpha Subunits / antagonists & inhibitors
  • Large-Conductance Calcium-Activated Potassium Channel alpha Subunits / metabolism*
  • Male
  • Middle Aged
  • Muscle Relaxation / drug effects
  • Muscle Relaxation / physiology*
  • Peptides / pharmacology
  • Phosphorylation
  • Pyridines / pharmacology
  • Rats, Wistar
  • Receptors, Adrenergic, beta-3 / metabolism*
  • Species Specificity
  • Thiazoles / pharmacology
  • Urinary Bladder / drug effects
  • Urinary Bladder / metabolism
  • Urinary Bladder / physiology*
  • rho-Associated Kinases / antagonists & inhibitors
  • rho-Associated Kinases / metabolism*

Substances

  • Acetanilides
  • Adrenergic beta-3 Receptor Agonists
  • Amides
  • KCNMA1 protein, human
  • Kcnma1 protein, rat
  • Large-Conductance Calcium-Activated Potassium Channel alpha Subunits
  • Peptides
  • Pyridines
  • Receptors, Adrenergic, beta-3
  • Thiazoles
  • Y 27632
  • iberiotoxin
  • rho-Associated Kinases
  • mirabegron