N(Omega)-nitro-l-arginine methyl ester potentiates lidocaine analgesic and anaesthetic effect in rats

J Pharm Pharmacol. 2023 Jan 31;75(1):98-104. doi: 10.1093/jpp/rgac082.

Abstract

Objectives: The purpose of the experiment was to study the effect of L-NAME (N(Omega)-nitro-L-arginine methyl ester) and its cotreatment with lidocaine on the spinal block and infiltrative cutaneous analgesia.

Methods: The quality of cutaneous analgesia was examined by the block of the cutaneous trunci muscle reflexes following needle stimuli in the rat. Spinal anaesthetic potency was assessed by measuring three neurobehavioral examinations of nociceptive, proprioceptive and motor function following intrathecal injection in the rat.

Key findings: L-NAME (0.6, 6 and 60 nmol) when cotreatment with lidocaine (ED50) produced dose-related cutaneous analgesia. Coadministration of L-NAME (0.6 μmol) with lidocaine intensified (P < 0.01) and prolonged (P < 0.001) cutaneous analgesia, whereas subcutaneous L-NAME (0.6 μmol) and saline did not provoke cutaneous analgesic effects. Adding L-NAME (2.5 μmol) to lidocaine intrathecally prolonged spinal sensory and motor block (P < 0.01), while intrathecal L-NAME (2.5 μmol) or 5% dextrose (vehicle) produced no spinal block.

Conclusions: L-NAME at 60 nmol (the minimum effective dose) increases and prolongs the effect of cutaneous analgesia of lidocaine. L-NANE at an ineffective dose potentiates lidocaine analgesic and anaesthetic effects.

Keywords: N(Omega)-nitro-l-arginine methyl ester; infiltrative cutaneous analgesia; lidocaine; spinal block.

MeSH terms

  • Analgesics / pharmacology
  • Analgesics / therapeutic use
  • Anesthetics* / therapeutic use
  • Animals
  • Lidocaine* / pharmacology
  • NG-Nitroarginine Methyl Ester / pharmacology
  • Pain / chemically induced
  • Pain / drug therapy
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Lidocaine
  • NG-Nitroarginine Methyl Ester
  • Analgesics
  • Anesthetics