Alteration in TRPV1 and Muscarinic (M3) receptor expression and function in idiopathic overactive bladder urothelial cells

Acta Physiol (Oxf). 2013 Jan;207(1):123-9. doi: 10.1111/j.1748-1716.2012.02462.x. Epub 2012 Jul 12.

Abstract

Aim: To examine function of both cholinergic (muscarinic) and TRPV1 receptors in human bladder urothelial (HBUC) from non-neurogenic overactive bladder (OAB) patients as compared to control subjects.

Methods: Primary HBUC cultures were derived from cystoscopic biopsies from OAB and control subjects. Muscarinic and TRPV1 function was assessed by acetylcholine (5 μm) or capsaicin (0.5 μm) evoked ATP release, measured by luciferase assay. Overall, expression of TRPV1 and muscarinic M3 receptors in bladder urothelial cells was accomplished using western immunoblotting.

Results: Our findings revealed that the response to acetylcholine in OAB HBUC cultures (which was blocked by the nonselective muscarinic antagonist, atropine methyl nitrate or AMN) was not significantly different than from controls. The acetylcholine M3 receptor was slightly decreased as compared to control. In contrast, OAB HBUC cultures exhibited a capsaicin hypersensitivity and augmented release of ATP (3.2 fold higher), which was blocked by the antagonist capsazepine. The increase in capsaicin sensitivity correlated with increased urothelial TRPV1 expression.

Conclusion: Though characterized in a small number of subjects, augmented release of urothelial-derived transmitters such as ATP could 'amplify' signalling between and within urothelial cells and nearby afferent nerves.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholine / pharmacology
  • Adenosine Triphosphate / metabolism
  • Adult
  • Capsaicin / pharmacology
  • Cholinergic Agonists / pharmacology
  • Epithelial Cells / drug effects
  • Epithelial Cells / metabolism
  • Humans
  • Middle Aged
  • Primary Cell Culture
  • Receptor, Muscarinic M3 / metabolism*
  • Sensory System Agents / pharmacology
  • Stimulation, Chemical
  • TRPV Cation Channels / metabolism*
  • Urinary Bladder, Overactive / drug therapy
  • Urinary Bladder, Overactive / metabolism*
  • Urinary Bladder, Overactive / physiopathology
  • Urothelium / drug effects
  • Urothelium / metabolism*
  • Urothelium / physiopathology

Substances

  • Cholinergic Agonists
  • Receptor, Muscarinic M3
  • Sensory System Agents
  • TRPV Cation Channels
  • TRPV1 protein, human
  • Adenosine Triphosphate
  • Acetylcholine
  • Capsaicin