Literature DB >> 7862859

Pharmacological analysis of the rate-decreasing effects of mu and kappa opioids in pigeons.

A J Mattox1, M J Picker, L A Dykstra.   

Abstract

The present study investigated the rate-decreasing effects of several mu (morphine and l-methadone) and kappa (bremazocine, U69,593 and U50,488) opioid agonists in pigeons. Mu and kappa agonists were examined alone, in combination with naltrexone or the mu-selective opioid antagonist, beta-funaltrexamine (beta-FNA), and in pigeons treated chronically with U50,488. Naltrexone was equipotent in shifting the morphine, l-methadone and bremazocine dose-effect curves to the right, but was less potent in shifting the U69,593 dose-effect curve and did not shift the U50,488 dose-effect curve. Beta-FNA shifted the l-methadone dose-effect curve to the right but did not shift the bremazocine, U69,593 or U50,488 dose-effect curves. Pigeons that developed tolerance to U50,488 following daily administration were cross-tolerant to bremazocine but not to l-methadone. Taken together, these experiments indicate that the rate-decreasing effects of morphine and l-methadone are mediated by mu opioid receptors, whereas the rate-decreasing effects of bremazocine, U69,593 and U50,488 in pigeons differ depending on the pharmacological procedures used to assess their effects.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 7862859     DOI: 10.1007/bf02245223

Source DB:  PubMed          Journal:  Psychopharmacology (Berl)        ISSN: 0033-3158            Impact factor:   4.530


  37 in total

Review 1.  Selective opioid receptor agonists and antagonists: research tools and potential therapeutic agents.

Authors:  D M Zimmerman; J D Leander
Journal:  J Med Chem       Date:  1990-03       Impact factor: 7.446

2.  The effects of morphine- and nalorphine- like drugs in the nondependent and morphine-dependent chronic spinal dog.

Authors:  W R Martin; C G Eades; J A Thompson; R E Huppler; P E Gilbert
Journal:  J Pharmacol Exp Ther       Date:  1976-06       Impact factor: 4.030

3.  Quantitative analysis of naloxone antagonism of the discriminative stimulus properties of morphine in the pigeon.

Authors:  W D Wessinger; D E McMillan
Journal:  Pharmacol Biochem Behav       Date:  1986-07       Impact factor: 3.533

4.  The binding spectrum of narcotic analgesic drugs with different agonist and antagonist properties.

Authors:  J Magnan; S J Paterson; A Tavani; H W Kosterlitz
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1982-06       Impact factor: 3.000

5.  Evidence that the discriminative stimulus properties of fentanyl and ethylketocyclazocine are mediated by an interaction with different opiate receptors.

Authors:  G T Shearman; A Herz
Journal:  J Pharmacol Exp Ther       Date:  1982-06       Impact factor: 4.030

6.  Comparison of the discriminative stimulus properties of U50,488 and morphine in pigeons.

Authors:  M Picker; L A Dykstra
Journal:  J Pharmacol Exp Ther       Date:  1987-12       Impact factor: 4.030

7.  Butorphanol, levallorphan, nalbuphine and nalorphine as antagonists in the squirrel monkey.

Authors:  L A Dykstra
Journal:  J Pharmacol Exp Ther       Date:  1990-07       Impact factor: 4.030

8.  Attenuation of the antinociceptive action of the selective kappa-opioid receptor agonist, U-50,488H by ICS-205-930.

Authors:  B Y Ho; A E Takemori
Journal:  Eur J Pharmacol       Date:  1990-03-27       Impact factor: 4.432

9.  U-50,488: a selective and structurally novel non-Mu (kappa) opioid agonist.

Authors:  P F Vonvoigtlander; R A Lahti; J H Ludens
Journal:  J Pharmacol Exp Ther       Date:  1983-01       Impact factor: 4.030

10.  U-50,488, a selective kappa opioid agonist: comparison to other reputed kappa agonists.

Authors:  P F Von Voigtlander; R A Lewis
Journal:  Prog Neuropsychopharmacol Biol Psychiatry       Date:  1982       Impact factor: 5.067

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.