β-Adrenoceptor-Mediated Relaxation of Carbachol-Pre-Contracted Mouse Detrusor

Urol Int. 2015;95(1):92-8. doi: 10.1159/000369075. Epub 2015 Jan 30.

Abstract

Aims: To study the β-adrenoceptor subtypes involved in the relaxation responses to (-)-isoprenaline in carbachol-pre-contracted (CCh) mouse detrusor muscle with intact and denuded mucosa.

Methods: Isolated muscle strips from the urinary bladder of male C57BL6 mice or β2-adrenoceptor knockout mice were pre-contracted with CCh, 1 µM and relaxed with increasing concentrations of the β-adrenoceptor (β-AR) agonist (-)-isoprenaline and forskolin. For estimating the β-AR subtypes involved, subtype-selective receptor blockers were used, that is, CGP 20712A (β1-ARs), ICI 118,551 (β2-ARs), and L748,337 (β3-ARs).

Results: Unlike in KCl-pre-contracted muscle, the mucosa did not affect the sensitivity of the relaxation response to (-)-isoprenaline in CCh-pre-contracted murine detrusor strips. Increasing concentrations of (-)-isoprenaline produced a biphasic concentration-relaxation response without any difference both during the presence and absence of mucosa. The relaxation fraction produced by low (-)-isoprenaline concentrations was mediated by β2-AR as evidenced by a shift of the concentration-response curve to higher concentrations with ICI 118,551, but not with CGP 20712A and L748,337, and by the absence of this fraction in β2-AR-KO mice. The relaxation response with low sensitivity to (-)-isoprenaline was not affected by any of the β-AR subtype-selective blockers and was the only response detected in detrusor strips from β2-AR-KO mice.

Conclusions: In CCh-pre-contracted mouse detrusor, β2-ARs are responsible for the relaxation component with high sensitivity to (-)-isoprenaline as indicated by the conversion of a biphasic into a monophasic CRC with ICI 118,551 or by its absence in β2-AR KO mice. The mucosa does not impair relaxation under these conditions.

MeSH terms

  • Aminophenols / chemistry
  • Animals
  • Carbachol / chemistry*
  • Cholinergic Agonists / chemistry
  • Colforsin / chemistry
  • Homozygote
  • Imidazoles / chemistry
  • Isoproterenol / chemistry
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mucous Membrane / pathology
  • Muscle Contraction / drug effects
  • Muscle Relaxation / drug effects*
  • Muscle, Smooth / pathology*
  • Propanolamines / chemistry
  • Receptors, Adrenergic, beta / metabolism*
  • Receptors, Adrenergic, beta-2 / genetics
  • Sulfonamides / chemistry
  • Urinary Bladder / drug effects*
  • Urinary Bladder / physiopathology

Substances

  • Aminophenols
  • Cholinergic Agonists
  • Imidazoles
  • L 748,337
  • Propanolamines
  • Receptors, Adrenergic, beta
  • Receptors, Adrenergic, beta-2
  • Sulfonamides
  • Colforsin
  • ICI 118551
  • Carbachol
  • CGP 20712A
  • Isoproterenol