| Literature DB >> 25557763 |
Sabatino Maione1, Lilyana Radanova2, Danilo De Gregorio1, Livio Luongo1, Luciano De Petrocellis3, Vincenzo Di Marzo4, Peter Imming2.
Abstract
The molecular mechanism of action of dipyrone, a widely used antipyretic and non-opioid analgesic drug, is still not fully understood. Actions upon peripheral inflamed tissues as well as the central nervous system, especially upon the PAG-RVM axis, have been suggested. Dipyrone is a prodrug and its activity is due to its immediate conversion to its active metabolites. We tested the effect of two recently discovered metabolites of dipyrone, the arachidonoyl amides of 4-methylaminoantipyrine and 4-aminoantipyrine, on the neurons of the rostral ventromedial medulla (RVM), which are part of the descending pathway of antinociception. These compounds reduced the activity of ON-cells and increased the activity of OFF-cells. Both CB1 and TRPV1 blockade reversed these effects, suggesting that the endocannabinoid/endovanilloid system takes part in the analgesic effects of dipyrone.Entities:
Keywords: Analgesia; Arachidonic acid amides; Dipyrone; Periaqueductal gray; Rostral ventromedial medulla
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Year: 2014 PMID: 25557763 DOI: 10.1016/j.ejphar.2014.12.022
Source DB: PubMed Journal: Eur J Pharmacol ISSN: 0014-2999 Impact factor: 4.432