Differential antagonism of opioid delta antinociception by [D-Ala2,Leu5, Cys6]enkephalin and naltrindole 5'-isothiocyanate: Evidence for delta receptor subtypes

Q. Jiang, A. E. Takemori, M. Sultana, P. S. Portoghese, W. D. Bowen, H. I. Mosberg, Frank Porreca

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Abstract

The present study has investigated the direct opioid delta receptor-mediated antinociception produced by i.c.v. administration of the highly selective delta agonists, [D-Pen2,D-Pen5]enkephalin (DPDPE) and [D-Ala2]deltorphin II, as well as that of the less delta-selective [D-Ser2,Leu5,Thr6]enkephalin (DSLET), by using two novel nonequilibrium opioid antagonists, [D-Ala2,Leu5,Cys6] enkephalin (DALCE) and naltrindole 5'-isothiocyanate (5'-NTII). At times ranging from 8 to 48 hr after a single i.c.v. pretreatment of mice with 5'-NTII, the antinociceptive effects of [D-Ala2] deltorphin II were significantly antagonized. In contrast, 5'-NTII pretreatment at times between 10 min and 24 hr failed to antagonize the antinociceptive effects of DPDPE. Previous studies have shown that pretreatment with i.c.v. DALCE produces a dose- and time-related antagonism of DPDPE, but not morphine, antinociception. However, pretreatment with i.c.v. DALCE failed to antagonize the antinociceptive effects of [D-Ala2]deltorphin II. Similarly, i.c.v. administration of DSLET produced time- and dose-related antinociception which was partially antagonized by either β-funaltrexamine (β-FNA) or by ICI 174,864 (N,N-diallyl-Tyr-Aib-Aib-Phe-Leu-OH), suggesting mixed activity at mu and delta receptors. ICI 174,864 produced essentially complete antagonism of DSLET antinociception in β-FNA-pretreated mice. Pretreatment with 5'-NTII (at -8 to -48 hr), blocked the antinociception produced by DSLET in control or in β-FNA-pretreated mice. In contrast, pretreatment with DALCE failed to antagonize the antinociception produced by i.c.v. DSLET in either control or in β-FNA-pretreated mice. These data show that the antinociceptive actions of [D-Ala2]deltorphin II and of DSLET are sensitive to the novel delta antagonist, 5'-NTII but not to DALCE. In contrast, the antinociception of DPDPE is sensitive to DALCE, but not to 5'-NTII. The differential antagonism of antinociception produced by these selective delta agonists suggests the existence of delta receptor subtypes.

Original languageEnglish (US)
Pages (from-to)1069-1075
Number of pages7
JournalJournal of Pharmacology and Experimental Therapeutics
Volume257
Issue number3
StatePublished - 1991

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delta Opioid Receptor
Enkephalins
Opioid Analgesics
D-Penicillamine (2,5)-Enkephalin
naltrindole 5'-isothiocyanate
Narcotic Antagonists
mu Opioid Receptor
Morphine

ASJC Scopus subject areas

  • Pharmacology

Cite this

Differential antagonism of opioid delta antinociception by [D-Ala2,Leu5, Cys6]enkephalin and naltrindole 5'-isothiocyanate : Evidence for delta receptor subtypes. / Jiang, Q.; Takemori, A. E.; Sultana, M.; Portoghese, P. S.; Bowen, W. D.; Mosberg, H. I.; Porreca, Frank.

In: Journal of Pharmacology and Experimental Therapeutics, Vol. 257, No. 3, 1991, p. 1069-1075.

Research output: Contribution to journalArticle

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abstract = "The present study has investigated the direct opioid delta receptor-mediated antinociception produced by i.c.v. administration of the highly selective delta agonists, [D-Pen2,D-Pen5]enkephalin (DPDPE) and [D-Ala2]deltorphin II, as well as that of the less delta-selective [D-Ser2,Leu5,Thr6]enkephalin (DSLET), by using two novel nonequilibrium opioid antagonists, [D-Ala2,Leu5,Cys6] enkephalin (DALCE) and naltrindole 5'-isothiocyanate (5'-NTII). At times ranging from 8 to 48 hr after a single i.c.v. pretreatment of mice with 5'-NTII, the antinociceptive effects of [D-Ala2] deltorphin II were significantly antagonized. In contrast, 5'-NTII pretreatment at times between 10 min and 24 hr failed to antagonize the antinociceptive effects of DPDPE. Previous studies have shown that pretreatment with i.c.v. DALCE produces a dose- and time-related antagonism of DPDPE, but not morphine, antinociception. However, pretreatment with i.c.v. DALCE failed to antagonize the antinociceptive effects of [D-Ala2]deltorphin II. Similarly, i.c.v. administration of DSLET produced time- and dose-related antinociception which was partially antagonized by either β-funaltrexamine (β-FNA) or by ICI 174,864 (N,N-diallyl-Tyr-Aib-Aib-Phe-Leu-OH), suggesting mixed activity at mu and delta receptors. ICI 174,864 produced essentially complete antagonism of DSLET antinociception in β-FNA-pretreated mice. Pretreatment with 5'-NTII (at -8 to -48 hr), blocked the antinociception produced by DSLET in control or in β-FNA-pretreated mice. In contrast, pretreatment with DALCE failed to antagonize the antinociception produced by i.c.v. DSLET in either control or in β-FNA-pretreated mice. These data show that the antinociceptive actions of [D-Ala2]deltorphin II and of DSLET are sensitive to the novel delta antagonist, 5'-NTII but not to DALCE. In contrast, the antinociception of DPDPE is sensitive to DALCE, but not to 5'-NTII. The differential antagonism of antinociception produced by these selective delta agonists suggests the existence of delta receptor subtypes.",
author = "Q. Jiang and Takemori, {A. E.} and M. Sultana and Portoghese, {P. S.} and Bowen, {W. D.} and Mosberg, {H. I.} and Frank Porreca",
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N2 - The present study has investigated the direct opioid delta receptor-mediated antinociception produced by i.c.v. administration of the highly selective delta agonists, [D-Pen2,D-Pen5]enkephalin (DPDPE) and [D-Ala2]deltorphin II, as well as that of the less delta-selective [D-Ser2,Leu5,Thr6]enkephalin (DSLET), by using two novel nonequilibrium opioid antagonists, [D-Ala2,Leu5,Cys6] enkephalin (DALCE) and naltrindole 5'-isothiocyanate (5'-NTII). At times ranging from 8 to 48 hr after a single i.c.v. pretreatment of mice with 5'-NTII, the antinociceptive effects of [D-Ala2] deltorphin II were significantly antagonized. In contrast, 5'-NTII pretreatment at times between 10 min and 24 hr failed to antagonize the antinociceptive effects of DPDPE. Previous studies have shown that pretreatment with i.c.v. DALCE produces a dose- and time-related antagonism of DPDPE, but not morphine, antinociception. However, pretreatment with i.c.v. DALCE failed to antagonize the antinociceptive effects of [D-Ala2]deltorphin II. Similarly, i.c.v. administration of DSLET produced time- and dose-related antinociception which was partially antagonized by either β-funaltrexamine (β-FNA) or by ICI 174,864 (N,N-diallyl-Tyr-Aib-Aib-Phe-Leu-OH), suggesting mixed activity at mu and delta receptors. ICI 174,864 produced essentially complete antagonism of DSLET antinociception in β-FNA-pretreated mice. Pretreatment with 5'-NTII (at -8 to -48 hr), blocked the antinociception produced by DSLET in control or in β-FNA-pretreated mice. In contrast, pretreatment with DALCE failed to antagonize the antinociception produced by i.c.v. DSLET in either control or in β-FNA-pretreated mice. These data show that the antinociceptive actions of [D-Ala2]deltorphin II and of DSLET are sensitive to the novel delta antagonist, 5'-NTII but not to DALCE. In contrast, the antinociception of DPDPE is sensitive to DALCE, but not to 5'-NTII. The differential antagonism of antinociception produced by these selective delta agonists suggests the existence of delta receptor subtypes.

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