Morphine state-dependent learning sensitization and interaction with nitric oxide

Pharmacology. 2006;78(2):66-71. doi: 10.1159/000095541. Epub 2006 Aug 4.

Abstract

In the present study, the effects of nitric oxide (NO) precursor L-arginine and L-NAME, a potent inhibitor of NO synthase (NOS), on the expression of sensitization of morphine were investigated. Pre-training administration of morphine (5 mg/kg) impaired memory retrieval compared to pre-training saline-treated animals. Amnesia due to pre-training morphine (5 mg/kg) was restored by pre-test morphine (5 mg/kg). The retrieval impairment was also inhibited in mice which had received once-daily injections of morphine (20 and 30 mg/kg, s.c.) for 3 days, followed by 5 days of no drug treatment before training (in order to induce morphine sensitization). Administration of L-arginine (60 mg/kg/day - 3 days) or L-NAME (20 mg/kg/day - 3 days) before training did not alter morphine state dependency. During acquisition of sensitization, administration of L-arginine (60 mg/kg) 20 min before morphine (10 mg/kg/day, for 3 days) increased, while injection of L-NAME (20 mg/kg) 20 min before morphine (30 mg/kg/day, for 3 days) decreased morphine state dependency. It is concluded that NO is involved in the morphine-induced sensitization.

MeSH terms

  • Animals
  • Arginine / pharmacology
  • Avoidance Learning / drug effects*
  • Behavior, Animal / drug effects*
  • Drug Interactions
  • Enzyme Inhibitors / pharmacology
  • Male
  • Memory / drug effects*
  • Mice
  • Mice, Inbred Strains
  • Morphine / pharmacology*
  • Morphine Dependence* / metabolism
  • Morphine Dependence* / physiopathology
  • NG-Nitroarginine Methyl Ester / pharmacology
  • Nitric Oxide / metabolism*
  • Nitric Oxide Synthase / antagonists & inhibitors

Substances

  • Enzyme Inhibitors
  • Nitric Oxide
  • Morphine
  • Arginine
  • Nitric Oxide Synthase
  • NG-Nitroarginine Methyl Ester