Literature DB >> 7874523

Stimulus intensity and the comparative efficacy of mu- and kappa-opioid agonists on nociceptive spinal reflexes in the rat.

S A Thorn1, J F Herrero, P M Headley.   

Abstract

The influence of stimulus intensity was tested on the relative spinal efficacy of intravenously administered mu- (fentanyl) and kappa-opioid (U-50,488) agonists. Spinal reflexes were generated by different intensities of noxious electrical stimuli in alpha-chloralose anaesthetized, spinalized rats. Both drugs became less effective as the intensity of C-fibre generated responses was increased, but U-50,488 retained the ability to reduce responses to the same degree as fentanyl. The effects were naloxone reversible. The results indicate that kappa-opioid receptor activation has similar potential for spinal analgesia as does activation of mu-opioid receptors.

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Year:  1994        PMID: 7874523     DOI: 10.1016/0006-8993(94)91286-6

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


  3 in total

1.  Subeffective doses of dexketoprofen trometamol enhance the potency and duration of fentanyl antinociception.

Authors:  Gema Gaitán; Juan F Herrero
Journal:  Br J Pharmacol       Date:  2002-01       Impact factor: 8.739

2.  NCX-701 (nitroparacetamol) is an effective antinociceptive agent in rat withdrawal reflexes and wind-up.

Authors:  E Alfonso Romero-Sandoval; Javier Mazario; David Howat; Juan F Herrero
Journal:  Br J Pharmacol       Date:  2002-03       Impact factor: 8.739

3.  Reversal by naloxone of the spinal antinociceptive actions of a systemically-administered NSAID.

Authors:  J F Herrero; P M Headley
Journal:  Br J Pharmacol       Date:  1996-06       Impact factor: 8.739

  3 in total

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