Attenuation of morphine tolerance and dependence with the highly selective delta-opioid receptor antagonist TIPP[psi]
- PMID: 8566146
- DOI: 10.1016/0014-2999(95)00554-x
Attenuation of morphine tolerance and dependence with the highly selective delta-opioid receptor antagonist TIPP[psi]
Abstract
We examined the effects of i.c.v. treatment with naltrindole, and the two highly selective peptide delta-opioid receptor antagonists H-Tyr-Tic-Phe-Phe-OH (TIPP) and H-Tyr-Tic psi [CH2-NH]-Phe-Phe- OH (TIPP[psi]), on the development of morphine tolerance and dependence. Each treatment significantly decreased naloxone-precipitated withdrawal, with TIPP[psi] reducing the most symptoms. TIPP[psi], but neither naltrindole nor TIPP, attenuated the development of analgesic tolerance in the tail-flick test. These results suggest that delta-opioid receptors are critically involved in the development of morphine tolerance and dependence.
Similar articles
-
The opioid mu agonist/delta antagonist DIPP-NH(2)[Psi] produces a potent analgesic effect, no physical dependence, and less tolerance than morphine in rats.J Med Chem. 1999 Sep 9;42(18):3520-6. doi: 10.1021/jm980724+. J Med Chem. 1999. PMID: 10479285
-
The TIPP opioid peptide family: development of delta antagonists, delta agonists, and mixed mu agonist/delta antagonists.Biopolymers. 1999;51(6):411-25. doi: 10.1002/(SICI)1097-0282(1999)51:6<411::AID-BIP4>3.0.CO;2-Z. Biopolymers. 1999. PMID: 10797230 Review.
-
Comparative analysis of various proposed models of the receptor-bound conformation of H-Tyr-Tic-Phe-OH related delta-opioid antagonists.Biopolymers. 1995;37(6):391-400. doi: 10.1002/bip.360370606. Biopolymers. 1995. PMID: 8589244
-
Agonist Activity of the delta-antagonists TIPP and TIPP-psi in cellular models expressing endogenous or transfected delta-opioid receptors.J Pharmacol Exp Ther. 2001 Jul;298(1):240-8. J Pharmacol Exp Ther. 2001. PMID: 11408548
-
Subtleties of structure-agonist versus antagonist relationships of opioid peptides and peptidomimetics.J Recept Signal Transduct Res. 1999 Jan-Jul;19(1-4):573-88. doi: 10.3109/10799899909036673. J Recept Signal Transduct Res. 1999. PMID: 10071786 Review.
Cited by
-
14-Alkoxy- and 14-acyloxypyridomorphinans: μ agonist/δ antagonist opioid analgesics with diminished tolerance and dependence side effects.J Med Chem. 2012 Oct 11;55(19):8350-63. doi: 10.1021/jm300686p. Epub 2012 Sep 27. J Med Chem. 2012. PMID: 23016952 Free PMC article.
-
Tryptophan Substitution in CJ-15,208 (cyclo[Phe-D-Pro-Phe-Trp]) Introduces δ-Opioid Receptor Antagonism, Preventing Antinociceptive Tolerance and Stress-Induced Reinstatement of Extinguished Cocaine-Conditioned Place Preference.Pharmaceuticals (Basel). 2023 Aug 29;16(9):1218. doi: 10.3390/ph16091218. Pharmaceuticals (Basel). 2023. PMID: 37765026 Free PMC article.
-
Aromatic-Amine Pendants Produce Highly Potent and Efficacious Mixed Efficacy μ-Opioid Receptor (MOR)/δ-Opioid Receptor (DOR) Peptidomimetics with Enhanced Metabolic Stability.J Med Chem. 2020 Feb 27;63(4):1671-1683. doi: 10.1021/acs.jmedchem.9b01818. Epub 2020 Feb 10. J Med Chem. 2020. PMID: 31986033 Free PMC article.
-
Design, Synthesis and Functional Analysis of Cyclic Opioid Peptides with Dmt-Tic Pharmacophore.Molecules. 2020 Sep 17;25(18):4260. doi: 10.3390/molecules25184260. Molecules. 2020. PMID: 32957550 Free PMC article.
-
Chronic morphine treatment alters NMDA receptor-mediated synaptic transmission in the nucleus accumbens.J Neurosci. 1999 Oct 15;19(20):9081-9. doi: 10.1523/JNEUROSCI.19-20-09081.1999. J Neurosci. 1999. PMID: 10516325 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources