Literature DB >> 188521

Absence of morphine antagonism of prostaglandin E1-stimulated [3H]3',5'-cyclic adenosine monophosphate accumulation in a rat brain mince system.

J B Katz, G N Catravas.   

Abstract

Prostaglandin E1 (PGE1)-stimulated [3H]3',5'-cyclic adenosine monophosphate ([3H]cAMP) accumulation was studied in a rat brain mince system to determine if stimulation of net [3H]cAMP accumulation could be prevented or reversed by morphine. Incubated minces of whole brain minus cerebellum were prepared from naive, acutely morphine-treated, and morphine-tolerant and withdrawing rats. Basal levels of [3H]cAMP accumulation in the three groups were equal within experimental limits. Morphine addition to the PGE1-stimulated minces did not prevent or reverse stimulation of [3H]cAMP accumulation in any of the three experimental groups. The data do not support the thesis that PGE1-stimulated cAMP accumulation in brain is a locus of opiate action in the phenomena of opiate analgesia, tolerance, and dependence.

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Year:  1977        PMID: 188521     DOI: 10.1016/0006-8993(77)90905-2

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


  3 in total

1.  Interactions of opiates and prostaglandins E with regard to cyclic AMP in striatal tissue of rats in vitro.

Authors:  U Havemann; K Kuschinsky
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1978-03       Impact factor: 3.000

2.  Purine involvement in morphine antinociception.

Authors:  P Mantegazza; R Tammiso; F Zambotti; L Zecca; N Zonta
Journal:  Br J Pharmacol       Date:  1984-12       Impact factor: 8.739

3.  Methyl xanthines, adenosine 3',5'-cyclic monophosphate and the spinal transmission of nociceptive information.

Authors:  A W Duggan; B T Griersmith
Journal:  Br J Pharmacol       Date:  1979-09       Impact factor: 8.739

  3 in total

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