Activity of mu- and delta-opioid agonists in vas deferens from mice deficient in MOR gene

Br J Pharmacol. 2001 Apr;132(7):1485-92. doi: 10.1038/sj.bjp.0703966.

Abstract

1. Mice lacking the mu-opioid receptor have been recently generated. Centrally mediated responses of mu-opioid agonists are suppressed whereas some of the delta-opioid responses are preserved in these mutant mice. 2. The vas deferens bioassay has been used in this study to investigate the functional activity at a peripheral level of mu- and delta-opioid agonists in mice lacking mu-opioid receptors. 3. The different mu-opioid agonists evaluated, morphine, DAMGO, dermorphin and [Lys(7)]-dermorphin produced an inhibitory response in vas deferens from wild-type mice but had no relevant activity on vas deferens from mutant mice. 4. The selective delta-opioid agonists DPDPE, BUBU, deltorphin I, deltorphin II and [D-Met(2)]-deltorphin induced inhibitory effects in vas deferens from both wild-type and mutant mice. However, the biological activities of these ligands were slightly reduced in preparations from mutant mice. The inhibitory responses of all these delta-opioid agonists were prevented by the administration of the selective delta-opioid antagonist naltrindole. 5. These data indicate that delta-opioid agonists, but not mu-opioid agonists, are biologically active in vas deferens from mice lacking mu-opioid receptors. The decreased response of delta-agonists in mutant mice suggests that some cooperativity may exist between mu- and delta-opioid receptors in these vas deferens preparations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analgesics, Opioid / pharmacology
  • Animals
  • Dose-Response Relationship, Drug
  • Electric Stimulation
  • Enkephalin, Ala(2)-MePhe(4)-Gly(5)- / pharmacology
  • Enkephalin, D-Penicillamine (2,5)- / pharmacology
  • Female
  • Genotype
  • In Vitro Techniques
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred Strains
  • Mice, Mutant Strains
  • Morphine / pharmacology
  • Muscle Contraction / drug effects
  • Naltrexone / analogs & derivatives*
  • Naltrexone / pharmacology
  • Narcotic Antagonists / pharmacology
  • Oligopeptides / pharmacology
  • Receptors, Opioid, delta / agonists*
  • Receptors, Opioid, delta / antagonists & inhibitors
  • Receptors, Opioid, mu / agonists*
  • Receptors, Opioid, mu / deficiency
  • Receptors, Opioid, mu / genetics
  • Vas Deferens / drug effects*
  • Vas Deferens / physiology

Substances

  • Analgesics, Opioid
  • Narcotic Antagonists
  • Oligopeptides
  • Receptors, Opioid, delta
  • Receptors, Opioid, mu
  • dermorphin, Lys(7)-
  • Enkephalin, Ala(2)-MePhe(4)-Gly(5)-
  • tyrosyl-seryl(O-t-butyl)-glycyl-phenylalanyl-leucyl-threonine(O-t-butyl)
  • deltorphin I, Ala(2)-
  • deltorphin II, Ala(2)-
  • Naltrexone
  • Morphine
  • Enkephalin, D-Penicillamine (2,5)-
  • naltrindole