Literature DB >> 2824755

Involvement of adenosine in the spinal antinociceptive effects of morphine and noradrenaline.

M I Sweeney1, T D White, J Sawynok.   

Abstract

Intrathecal (i.t.) pretreatment of rats with either theophylline (50 micrograms) or 8-phenyltheophylline (3 micrograms) antagonized antinociception produced by i.t. injection of morphine (0.3-3 micrograms) in the tailflick and hotplate tests, but had no effect on antinociception produced by i.t. injection of noradrenaline (10-30 micrograms). In other experiments designed to test whether morphine released adenosine from the spinal cord, adenosine release from synaptosomes was measured by high-performance liquid chromatography with fluorescence detection of etheno-adenosine. Depolarization with 24 mM K+ or 50 microM veratridine released 3 times as much adenosine from dorsal than from ventral spinal cord synaptosomes. K+ released primarily adenosine whereas veratridine released both adenosine and nucleotide(s). Morphine (1-100 microM) produced a Ca++-dependent release of endogenous adenosine, comparable to K+-evoked adenosine release, which was blocked by 1 microM naltrexone. Noradrenaline (5-500 microM) produced a Ca++-dependent release of a nucleotide which was subsequently degraded extracellularly to adenosine by ecto-5'-nucleotidase. This release was antagonized by 10 microM phentolamine and by 1 microM yohimbine. These results suggest that, within the spinal cord, morphine may act on opioid receptors to release adenosine which subsequently acts at adenosine receptors to produce spinal analgesia. Spinal analgesia produced by noradrenaline does not appear to involve adenosine release.

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Year:  1987        PMID: 2824755

Source DB:  PubMed          Journal:  J Pharmacol Exp Ther        ISSN: 0022-3565            Impact factor:   4.030


  5 in total

1.  The role of spinal inhibitory neuroreceptors in the antihyperalgesic effect of warm water immersion therapy.

Authors:  Fernanda Madeira; Rômulo Nolasco de Brito; Aline A Emer; Ana Paula Batisti; Bruna Lenfers Turnes; Afonso Shiguemi Inoue Salgado; Francisco José Cidral-Filho; Leidiane Mazzardo-Martins; Daniel Fernandes Martins
Journal:  Braz J Phys Ther       Date:  2020-02-12       Impact factor: 3.377

2.  Adenosine analogs do not inhibit the potassium-stimulated release of substance P from rat spinal cord slices.

Authors:  M R Vasko; H Ono
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1990-10       Impact factor: 3.000

3.  Chronic intrathecal morphine treatment does not cause down-regulation of spinal adenosine A1 receptors in rats.

Authors:  P L Tao; C S Wong; M C Lin
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1996-07       Impact factor: 3.000

Review 4.  Adenosine receptors: Emerging non-opioids targets for pain medications.

Authors:  Soo-Min Jung; Lee Peyton; Hesham Essa; Doo-Sup Choi
Journal:  Neurobiol Pain       Date:  2022-03-25

5.  Spinal A3 adenosine receptor activation acutely restores morphine antinociception in opioid tolerant male rats.

Authors:  Heather Leduc-Pessah; Cynthia Xu; Churmy Y Fan; Rebecca Dalgarno; Yuta Kohro; Sydney Sparanese; Nikita N Burke; Kenneth A Jacobson; Christophe Altier; Daniela Salvemini; Tuan Trang
Journal:  J Neurosci Res       Date:  2021-06-01       Impact factor: 4.433

  5 in total

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