The peripheral administration of a nitric oxide donor potentiates the local antinociceptive effects of a DOR agonist during chronic inflammatory pain in mice

Naunyn Schmiedebergs Arch Pharmacol. 2009 Oct;380(4):345-52. doi: 10.1007/s00210-009-0436-6. Epub 2009 Jul 28.

Abstract

Several works reveal that nitric oxide could enhance the peripheral antinociception induced by opioids during acute inflammation. Nonetheless, the role of nitric oxide in the local antinociceptive effects of delta-opioid receptor (DOR) agonists during chronic peripheral inflammation is not known. The aim of this study is to evaluate whether nitric oxide would enhance the local antinociceptive effects of a DOR agonist during chronic inflammatory pain in mice. Chronic inflammatory pain was induced by the subplantar administration of complete Freund's adjuvant (CFA; 30 microl) and thermal hyperalgesia assessed by plantar test. In C57BL/6J mice, we evaluated the local antinociceptive effects of a DOR agonist, [D-Pen2,5]-enkephalin (DPDPE) and a nitric oxide donor, DETA NONOate DETA/NO 2,2'-(hydroxynitrosohydrazino) Bis-Ethanamine (NOC-18) alone or combined (DPDPE plus NOC-18) at 1, 4, 7, and 10 days after CFA injection. The reversibility of the peripheral antinociceptive effects of DPDPE, alone or combined with NOC-18, was assessed with the local administration of selective (naltrindole) and non-selective (naloxone methiodide) DOR antagonists. The local administration of DPDPE or NOC-18 alone dose-dependently inhibited the thermal hyperalgesia induced by peripheral inflammation. Moreover, the co-administration of NOC-18 with DPDPE significantly increased the antinociceptive effects produced by DPDPE from 1 to 10 days of CFA-induced inflammatory pain (P < 0.05). These effects were completely blocked by naltrindole and naloxone methiodide. Our results demonstrate that nitric oxide might enhance the local antinociceptive effects of a DOR agonist during chronic inflammatory pain by interaction with peripheral DOR, representing a useful strategy for an efficient antinociceptive treatment of peripheral inflammatory pain.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analgesics, Opioid / administration & dosage*
  • Animals
  • Chronic Disease
  • Disease Models, Animal
  • Drug Therapy, Combination
  • Enkephalin, D-Penicillamine (2,5)- / administration & dosage*
  • Freund's Adjuvant
  • Hot Temperature
  • Hyperalgesia / drug therapy*
  • Hyperalgesia / etiology
  • Hyperalgesia / metabolism
  • Inflammation / chemically induced
  • Inflammation / drug therapy*
  • Inflammation / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Naltrexone / administration & dosage
  • Naltrexone / analogs & derivatives
  • Narcotic Antagonists / administration & dosage
  • Nitric Oxide / metabolism*
  • Nitric Oxide Donors / administration & dosage*
  • Nitric Oxide Donors / metabolism
  • Nitroso Compounds / administration & dosage*
  • Nitroso Compounds / metabolism
  • Pain Measurement
  • Receptors, Opioid, delta / agonists*
  • Receptors, Opioid, delta / metabolism
  • Time Factors

Substances

  • Analgesics, Opioid
  • NOC 18
  • Narcotic Antagonists
  • Nitric Oxide Donors
  • Nitroso Compounds
  • Receptors, Opioid, delta
  • Nitric Oxide
  • Naltrexone
  • Enkephalin, D-Penicillamine (2,5)-
  • Freund's Adjuvant
  • naltrindole