α2-Adrenoceptor modulation of nociception in rat spinal cord: location, effects and interactions with morphine

https://doi.org/10.1016/0014-2999(87)90430-4Get rights and content

Abstract

The effects of intrathecal clonidine alone and prior to intrathecal morphine were studied on electrically evoked Aβ and C fibre activity in the dorsal horn of the halothane-anaesthetised rat. Clonidine reduced C fibre-evoked activity in a dose-dependent manner, to a maximum 52% inhibition which was reversed by rauwolscine and yohimbine but not naloxone. High dose of clonidine also produced small inhibitions of A fibre-evoked activity. Clonidine potentiated the inhibitory action of intrathecal morphine on electrically evoked C fibre activity but not A fibre activity. In addition, the location of α2-adrenoceptor and opiate binding sites in consecutive sections of rat lumbar cord was investigated using in vitro autoradiography with selective ligands, and it was demonstrated that both opiate and α2-receptor types are present within the same superficial layers of the dorsal horn of the same animal. The results indicate that α2-adrenoceptors and opiate receptors can interact in the modulation of nociceptive transmission in rat spinal cord.

References (36)

Cited by (179)

  • α<inf>2</inf>-agonists and antagonists

    2022, Small Animal Critical Care Medicine
  • Activation of a Gq-coupled membrane estrogen receptor rapidly attenuates α<inf>2</inf>-adrenoceptor-induced antinociception via an ERK I/II-dependent, non-genomic mechanism in the female rat

    2014, Neuroscience
    Citation Excerpt :

    These findings, together with our current data, would suggest that the Gq-mER-mediated rapid and reversible suppression of clonidine-mediated antinociception depends primarily on non-genomic mechanisms. The α2-adrenoceptor is widely distributed in the brain and spinal cord, including the dorsal horn (Unnerstall et al., 1984; Sullivan et al., 1987; Stone et al., 1998). Consequently, epidural or i.t. clonidine treatment has been utilized to alleviate severe neuropathic or cancer pain even in patients with limited relief by and development of tolerance to opiates (Rauck et al., 1993; Eisenach et al., 1995; Hassenbusch et al., 1999; Dobrydnjov et al., 2005).

  • α2 agonists and antagonists

    2014, Small Animal Critical Care Medicine, Second Edition
View all citing articles on Scopus
View full text