[Effects of pethidine on cardiac electrophysiological properties]

Zhejiang Da Xue Xue Bao Yi Xue Ban. 2003 Jun;32(3):207-11. doi: 10.3785/j.issn.1008-9292.2003.03.009.
[Article in Chinese]

Abstract

Objective: To investigate the effects of pethidine on electrophysiological properties of the isolated ventricular myocytes and the underlying mechanism.

Methods: Langendorff was applied to perfuse rat heart model and whole-cell current clamp and voltage clamp techniques were used.

Results: Pethidine decreased heart rate (HR) in a concentration dependent manner and caused severe atrioventricular block (AVB) at >or=250 micromol/L. Pethidine reduced action potential amplitude and maximal rate of depolarization, prolonged action potential duration. Pethidine at 100 micromol/L decreased sodium currents (I(Na)), transient outward potassium currents (I(to)), delayed rectifier potassium currents (I(k)) and L-type calcium currents (I(Ca.L)) to (60.7+/-6.9)%, (55.4+/-5.6)%, (65.1+/-8.0)% and (67.4+/-10.1)% of control levels,respectively. These effects could be recovered by washout. Naloxone, an opioid receptor antagonist, could not abolish the effects of pethidine on ionic currents.

Conclusion: Pethidine decreased HR and induced AVB, which may be related to the inhibition of I(Na), I(to), I(k) and I(Ca-L) of heart. The depression of cardiac currents is not mediated by opioid receptor.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials / drug effects
  • Animals
  • Heart / drug effects*
  • Heart / physiology
  • Heart Block / chemically induced
  • Heart Rate / drug effects
  • In Vitro Techniques
  • Ion Channels / antagonists & inhibitors
  • Male
  • Meperidine / pharmacology*
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Opioid / physiology

Substances

  • Ion Channels
  • Receptors, Opioid
  • Meperidine