Pharmacological study of dihydroetorphine in cloned μ-, δ- and κ-opioid receptors
- 1 November 1995
- journal article
- research article
- Published by Elsevier in European Journal of Pharmacology: Molecular Pharmacology
- Vol. 291 (3) , 367-373
- https://doi.org/10.1016/0922-4106(95)90078-0
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- U-50,488 blocks the development of morphine tolerance and dependence at a very low dose in guinea pigsEuropean Journal of Pharmacology, 1994
- Antagonists at excitatory opioid receptors on sensory neurons in culture increase potency and specificity of opiate analgesics and attenuate development of tolerance/dependenceBrain Research, 1994
- Physical Dependence Produced by Dihydroetorphine in Mice.Biological & Pharmaceutical Bulletin, 1994
- Cloning and expression of a cDNA for the rat k‐opioid receptorFEBS Letters, 1993
- Primary structures and expression from cDNAs of rat opioid receptor δ‐and μ‐subtypesFEBS Letters, 1993
- Antinociceptive Effect of Dihydroetorphine and Its Tolerance/Dependence Liability in Mice.Biological & Pharmaceutical Bulletin, 1993
- Effects of nor-binaltorphimine on the development of analgesic tolerance to and physical dependence on morphineEuropean Journal of Pharmacology, 1992
- Analgesic synergy and improved motor function produced by combinations of μ-δ- and μ-κ-opioidsBrain Research, 1990
- κ- and δ-opioid agonists synergize to produce potent analgesiaBrain Research, 1990
- Novel analgesics and molecular rearrangements in the morphine-thebaine group. III. Alcohols of the 6,14-endo-ethenotetrahydrooripavine series and derived analogs of N-allylnormorphine and -norcodeineJournal of the American Chemical Society, 1967