Inhibition of nitric oxide synthase attenuates the development of morphine tolerance and dependence in mice

Neuropharmacology. 1994 Feb;33(2):189-92. doi: 10.1016/0028-3908(94)90006-x.

Abstract

The effect of the nitric oxide (NO) synthase inhibitor L-NG-nitroarginine methyl ester (L-NAME, 5-20 mg/kg i.p.) and NG-nitro-L-arginine (NO2Arg, 5-20 mg/kg i.p.) on morphine-induced analgesia, as well as on morphine induced tolerance and dependence was examined in male albino Swiss mice. Neither acute nor repeated (for 5 days) administration of the nitric oxide synthase inhibitor, L-NAME affected the morphine induced analgesia, as measured by hot plate and tail-flick tests. On the other hand, administration of L-NAME or NO2Arg along with morphine prevented the development of tolerance to the analgesic effect of morphine for at least 7 days, whereas the analgesic effect of morphine alone disappeared after 5 days. L-NAME and NO2Arg also attenuated some signs of morphine dependence, as assessed by naloxone (2 mg/kg)-precipitated withdrawal. These results indicate that NO may play a role in the development of morphine tolerance and dependence.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Oxidoreductases / antagonists & inhibitors*
  • Analysis of Variance
  • Animals
  • Arginine / analogs & derivatives
  • Arginine / pharmacology
  • Drug Tolerance
  • Male
  • Mice
  • Morphine / pharmacology*
  • Morphine Dependence / physiopathology
  • Morphine Dependence / prevention & control
  • NG-Nitroarginine Methyl Ester
  • Naloxone / pharmacology
  • Nitric Oxide / physiology*
  • Nitric Oxide Synthase
  • Nitroarginine

Substances

  • Nitroarginine
  • Nitric Oxide
  • Naloxone
  • Morphine
  • Arginine
  • Nitric Oxide Synthase
  • Amino Acid Oxidoreductases
  • NG-Nitroarginine Methyl Ester