Buprenorphine activates mu and opioid receptor like-1 receptors simultaneously, but the analgesic effect is mainly mediated by mu receptor activation in the rat formalin test

Buprenorphine activates mu and opioid receptor like-1 receptors simultaneously, but the analgesic effect is mainly mediated by mu receptor activation in the rat formalin test

Item
http://www.wikidata.org/entity/Q28572088
Endogenous opiates and behavior: 2006Nociceptin produces antinociception after spinal administration in amphibiansA double blind, within subject comparison of spontaneous opioid withdrawal from buprenorphine versus morphineBuprenorphine disrupts sleep and decreases adenosine concentrations in sleep-regulating brain regions of Sprague Dawley rat.Pronociceptive and Antinociceptive Effects of Buprenorphine in the Spinal Cord Dorsal Horn Cover a Dose Range of Four Orders of Magnitude.Roles of μ-opioid receptors and nociceptin/orphanin FQ peptide receptors in buprenorphine-induced physiological responses in primates.Bifunctional Peptide-Based Opioid Agonist-Nociceptin Antagonist Ligands for Dual Treatment of Acute and Neuropathic PainThe role of the opioid receptor-like (ORL1) receptor in motor stimulatory and rewarding actions of buprenorphine and morphineImpacts of anti-nerve growth factor antibody on pain-related behaviors and expressions of opioid receptor in spinal dorsal horn and dorsal root ganglia of rats with cancer-induced bone pain.Identification of an additional supraspinal component to the analgesic mechanism of action of buprenorphine.Activity of new NOP receptor ligands in a rat peripheral mononeuropathy model: potentiation of morphine anti-allodynic activity by NOP receptor antagonists.Evidence from basic research for opioid combinations.Effects of co-administration of intrathecal nociceptin/orphanin FQ and opioid antagonists on formalin-induced pain in rats.Buprenorphine is a weak partial agonist that inhibits opioid receptor desensitization.Buprenorphine for neuropathic pain--targeting hyperalgesia.Association analysis of genes encoding the nociceptin receptor (OPRL1) and its endogenous ligand (PNOC) with alcohol or illicit drug dependence.Collagen antibody-induced arthritis evokes persistent pain with spinal glial involvement and transient prostaglandin dependency.
P2860

Buprenorphine activates mu and opioid receptor like-1 receptors simultaneously, but the analgesic effect is mainly mediated by mu receptor activation in the rat formalin test

Item
http://www.wikidata.org/entity/Q28572088
description
2006 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2006
@ast
im Juli 2006 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2006/07/01)
@sk
vědecký článek publikovaný v roce 2006
@cs
wetenschappelijk artikel (gepubliceerd op 2006/07/01)
@nl
наукова стаття, опублікована в липні 2006
@uk
مقالة علمية (نشرت في يوليو 2006)
@ar
name
Buprenorphine activates mu and ...... ation in the rat formalin test
@ast
Buprenorphine activates mu and ...... ation in the rat formalin test
@en
Buprenorphine activates mu and ...... ation in the rat formalin test
@nl
type
label
Buprenorphine activates mu and ...... ation in the rat formalin test
@ast
Buprenorphine activates mu and ...... ation in the rat formalin test
@en
Buprenorphine activates mu and ...... ation in the rat formalin test
@nl
prefLabel
Buprenorphine activates mu and ...... ation in the rat formalin test
@ast
Buprenorphine activates mu and ...... ation in the rat formalin test
@en
Buprenorphine activates mu and ...... ation in the rat formalin test
@nl
P1433
P1476
P2093
P304
P31
P3181
P356
P407
P433
P478
P577
P5875
P698
P921
P3181
P356
P1433
P1476
Buprenorphine activates mu and ...... ation in the rat formalin test
@en
P2093
P304
P31
P3181
P356
P407
P433
P478
P577
P5875
P698
P921