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British Journal of Pharmacology
Article . 2008 . Peer-reviewed
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The μ‐opioid receptor agonist morphine, but not agonists at δ‐ or κ‐opioid receptors, induces peripheral antinociception mediated by cannabinoid receptors

Authors: D, da Fonseca Pacheco; A, Klein; A, de Castro Perez; C M, da Fonseca Pacheco; J N, de Francischi; I D G, Duarte;

The μ‐opioid receptor agonist morphine, but not agonists at δ‐ or κ‐opioid receptors, induces peripheral antinociception mediated by cannabinoid receptors

Abstract

Background and purpose:Although participation of opioids in antinociception induced by cannabinoids has been documented, there is little information regarding the participation of cannabinoids in the antinociceptive mechanisms of opioids. The aim of the present study was to determine whether endocannabinoids could be involved in peripheral antinociception induced by activation of μ‐, δ‐ and κ‐opioid receptors.Experimental approach:Nociceptive thresholds to mechanical stimulation of rat paws treated with intraplantar prostaglandin E2(PGE2, 2 μg) to induce hyperalgesia were measured 3 h after injection using an algesimetric apparatus. Opioid agonists morphine (200 μg), (+)‐4‐[(alphaR)‐alpha‐((2S,5R)‐4‐Allyl‐2,5‐dimethyl‐1‐piperazinyl)‐3‐
methoxybenzyl]‐N,N‐diethylbenzamide (SNC80) (80 μg), bremazocine (50 μg); cannabinoid receptor antagonistsN‐(piperidin‐1‐yl)‐5‐(4‐
iodophenyl)‐1‐(2,4‐dichlorophenyl)‐4‐methyl‐1H‐pyrazole‐3‐carboxamide (AM251) (20–80 μg), 6‐iodo‐2‐methyl‐1‐[2‐(4‐morpholinyl)
ethyl]‐1H‐indol‐3‐yl(4‐methoxyphenyl) methanone (AM630) (12.5–100 μg); and an inhibitor of methyl arachidonyl fluorophosphonate (MAFP) (1–4 μg) were also injected in the paw.Key results:The CB1‐selective cannabinoid receptor antagonist AM251 completely reversed the peripheral antinociception induced by morphine in a dose‐dependent manner. In contrast, the CB2‐selective cannabinoid receptor antagonist AM630 elicited partial antagonism of this effect. In addition, the administration of the fatty acid amide hydrolase inhibitor, MAFP, enhanced the antinociception induced by morphine. The cannabinoid receptor antagonists AM251 and AM630 did not modify the antinociceptive effect of SNC80 or bremazocine. The antagonists alone did not cause any hyperalgesic or antinociceptive effect.Conclusions and implications:Our results provide evidence for the involvement of endocannabinoids, in the peripheral antinociception induced by the μ‐opioid receptor agonist morphine. The release of cannabinoids appears not to be involved in the peripheral antinociceptive effect induced by κ‐ and δ‐opioid receptor agonists.British Journal of Pharmacology(2008)154, 1143–1149; doi:10.1038/bjp.2008.175; published online 12 May 2008

Keywords

Male, Indoles, Dose-Response Relationship, Drug, Morphine, Organophosphonates, Pain, Arachidonic Acids, Dinoprostone, Piperazines, Amidohydrolases, Analgesics, Opioid, Benzomorphans, Disease Models, Animal, Piperidines, Hyperalgesia, Benzamides, Cannabinoid Receptor Modulators, Animals, Enzyme Inhibitors, Pain Measurement

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    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
77
Top 10%
Top 10%
Top 10%
bronze