Literature DB >> 8891291

The effects of morphine on carrageenin-induced spinal c-Fos expression are completely blocked by beta-funaltrexamine, a selective mu-opioid receptor antagonist.

P Honoré1, J Buritova, J M Besson.   

Abstract

We have demonstrated that pre-administered morphine (3 mg/kg, i.v.) decreased spinal c-Fos expression induced 2 h after intraplantar carrageenin (55 +/- 5% reduction, P < 0.0001). These effects were completely blocked by pre-administered beta-funaltrexamine (10 mg/kg, i.v., 24 h prior to stimulation) a selective long-lasting mu-opioid receptor antagonist. In conclusion, these results clearly demonstrate that the effects of morphine on noxiously-evoked spinal c-Fos expression are essentially mediated via mu-opioid receptors.

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Year:  1996        PMID: 8891291     DOI: 10.1016/0006-8993(96)00749-4

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  1 in total

1.  Inflammatory hyperalgesia induces essential bioactive lipid production in the spinal cord.

Authors:  Matthew W Buczynski; Camilla I Svensson; Darren S Dumlao; Bethany L Fitzsimmons; Jae-Hang Shim; Thomas J Scherbart; Faith E Jacobsen; Xiao-Ying Hua; Tony L Yaksh; Edward A Dennis
Journal:  J Neurochem       Date:  2010-05-14       Impact factor: 5.372

  1 in total

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