Literature DB >> 7696628

Spinal serotonin IA and IC/2 receptors mediate supraspinal mu opioid-induced analgesia.

W Xu1, X Cui, J S Han.   

Abstract

Intracerebroventricular (i.c.v.) injection of highly selective mu opioid receptor agonist ohmefentanyl (OMF) to rats produced dose-dependent antinociception as assessed with the tail flick test. This analgesia could be blocked by intrathecal (i.t.) injection of the 5-HT1A receptor antagonist spiperone or the 5-HT1C/2 receptor antagonist mianserin, but not by the 5-HT2 receptor antagonist 1-NP or the 5-HT3 receptor antagonist ICS 205-930. The results suggest that the descending 5-HT system is involved in mediating spinal mu opioid analgesia via spinal 5-HT1A and 5-HT1C/2 receptors.

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Year:  1994        PMID: 7696628     DOI: 10.1097/00001756-199412000-00065

Source DB:  PubMed          Journal:  Neuroreport        ISSN: 0959-4965            Impact factor:   1.837


  3 in total

1.  Modulation of afferent-evoked neurotransmission by 5-HT3 receptors in young rat dorsal horn neurones in vitro: a putative mechanism of 5-HT3 induced anti-nociception.

Authors:  S G Khasabov; J A Lopez-Garcia; A U Asghar; A E King
Journal:  Br J Pharmacol       Date:  1999-06       Impact factor: 8.739

2.  Systemic morphine produce antinociception mediated by spinal 5-HT7, but not 5-HT1A and 5-HT2 receptors in the spinal cord.

Authors:  A Dogrul; M Seyrek
Journal:  Br J Pharmacol       Date:  2006-08-14       Impact factor: 8.739

3.  Effect of fentanyl on 5-HT efflux involves both opioid and 5-HT1A receptors.

Authors:  Rui Tao; Meghana Karnik; Zhiyuan Ma; Sidney B Auerbach
Journal:  Br J Pharmacol       Date:  2003-08       Impact factor: 8.739

  3 in total

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