Literature DB >> 2606149

Intrathecal porcine calcitonin enhances the release of [Met5]enkephalin-like material from the rat spinal cord.

E Collin1, S Bourgoin, P Gorce, M Hamon, F Cesselin.   

Abstract

Perfusion of the intrathecal space of halothane-anaesthetized rats with artificial cerebro-spinal fluid supplemented with porcine calcitonin (1-10 microM) produced a significant increase (+67-110%) in the spinal release of [Met5]enkephalin-like material. The effect of porcine calcitonin was markedly enhanced (+100%) in animals receiving a continuous i.v. infusion of the opioid antagonist naloxone (65 micrograms/kg per min). These data strongly suggest that the antinociceptive effect of intrathecal porcine calcitonin might involve a stimulatory action of the hormone on spinal enkephalinergic interneurones. In addition, presynaptic opioid autoreceptors probably control the activity of these neurones in the rat.

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Year:  1989        PMID: 2606149     DOI: 10.1016/0014-2999(89)90566-9

Source DB:  PubMed          Journal:  Eur J Pharmacol        ISSN: 0014-2999            Impact factor:   4.432


  3 in total

1.  Influence of pertussis toxin on the calcitonin-opioid interaction in isolated tissues.

Authors:  M I Martin; C Goicoechea; M J Ormazábal; M J Alfaro
Journal:  Br J Pharmacol       Date:  1996-11       Impact factor: 8.739

Review 2.  Calcitonin and its antinociceptive activity: animal and human investigations 1975-1992.

Authors:  P C Braga
Journal:  Agents Actions       Date:  1994-05

3.  In vitro study of the interaction of salmon calcitonin with mu, delta and kappa opioid agonists.

Authors:  M I Martín; M J Alfaro; C Goicoechea; M I Colado
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1993-03       Impact factor: 3.000

  3 in total

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