The role of cholinesterases in rat urinary bladder contractility

Urol Res. 2003 Jul;31(3):223-6. doi: 10.1007/s00240-003-0326-1. Epub 2003 May 8.

Abstract

This study examines the effects of inhibition of acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) on acetylcholine (ACh)-induced contraction in rat urinary bladder smooth muscle. Neostigmine, a non-selective ChE inhibitor, caused concentration-dependent contractions in rat urinary bladder strips, whereas tetraisopropylpyrophosphoramide (iso-OMPA; a BuChE inhibitor) failed to affect the resting tone of the preparations. Neostigmine (1 microM) markedly augmented the contractile responses to ACh. Although iso-OMPA (10 microM) also potentiated ACh-induced contraction, the effect was less than that evoked by neostigmine. The activities of AChE in rat urinary bladder strips were significantly (P<0.05) higher than those of BuChE. These results indicated that AChE, rather than BuChE, plays an important role in controlling ACh-induced contractions of rat urinary bladder.

MeSH terms

  • Acetylcholinesterase / metabolism
  • Acetylcholinesterase / physiology*
  • Animals
  • Butyrylcholinesterase / metabolism
  • Butyrylcholinesterase / physiology*
  • Cholinesterase Inhibitors / pharmacology
  • In Vitro Techniques
  • Male
  • Muscle Contraction / drug effects
  • Muscle Contraction / physiology*
  • Muscle, Smooth / physiology*
  • Neostigmine / pharmacology
  • Rats
  • Rats, Wistar
  • Tetraisopropylpyrophosphamide / pharmacology
  • Urinary Bladder / physiology*

Substances

  • Cholinesterase Inhibitors
  • Neostigmine
  • Tetraisopropylpyrophosphamide
  • Acetylcholinesterase
  • Butyrylcholinesterase