Intrathecal Tyr-W-MIF-1 produces potent, naloxone-reversible analgesia modulated by α2-adrenoceptors
- 18 March 1996
- journal article
- Published by Elsevier in European Journal of Pharmacology
- Vol. 298 (3) , 235-239
- https://doi.org/10.1016/0014-2999(95)00823-3
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- The Tyr-MIF-1 family of peptidesNeuroscience & Biobehavioral Reviews, 1995
- Cyclic analogues of Tyr-W-MIF-1 with prolonged analgesic activity and potency comparable to DAMGO and morphinePeptides, 1994
- Expression of the FOS proto-oncogene protein in brain after ICV administration of Tyr-W-MIF-1 (Tyr-Pro-Trp-Gly-NH2)Peptides, 1994
- Mu, delta, and kappa opiate receptor binding of Tyr-MIF-1 and of Tyr-W-MIF-1, its active fragments, and two potent analogsLife Sciences, 1994
- Isolation of a novel tetrapeptide with opiate and antiopiate activity from human brain cortex: Tyr-Pro-Trp-Gly-NH2 (Tyr-W-MIF-1)Peptides, 1992
- Comparison of naloxonazine and β-funaltrexamine antagonism of μ1 and μ2 opioid actionsLife Sciences, 1991
- Hemorphins, cytochrophins, and human beta-casomorphins bind to antiopiate (Tyr-MIF-1) as well as opiate binding sites in rat brainLife Sciences, 1989
- Characterization of the spinal adrenergic receptors mediating the spinal effects produced by the microinjection of morphine into the periaqueductal grayBrain Research, 1985
- Spinal 5-HT or NA Uptake Inhibition Potentiates Supraspinal Morphine Antinociception in RatsActa Pharmacologica et Toxicologica, 1984
- Endogenous opioid peptides: multiple agonists and receptorsNature, 1977