Endocannabinoid Research Group at the Department of Experimental Medicine, Division of Pharmacology "L. Donatelli", The Second University of Naples, 80138 Naples, Italy.
Institut fuer Pharmazie, Martin-Luther-Universitaet Halle, Germany.
Eur J Pharmacol. 2015 Feb 5;748:115-22. doi: 10.1016/j.ejphar.2014.12.022. Epub 2014 Dec 31.
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.
双氯芬酸作为一种广泛应用的解热和非阿片类镇痛药,其作用机制仍不完全清楚。有研究表明,它除了对周围炎性组织有作用外,对中枢神经系统,特别是 PAG-RVM 轴也有作用。双氯芬酸是一种前体药物,其活性是由于其立即转化为其活性代谢物。我们测试了双氯芬酸的两种新发现的代谢物,4-甲基氨基安替比林和 4-氨基安替比林的花生四烯酰酰胺,对延髓头端腹内侧区(RVM)神经元的影响,RVM 神经元是下行镇痛通路的一部分。这两种化合物降低了 ON 细胞的活性,增加了 OFF 细胞的活性。CB1 和 TRPV1 阻断均可逆转这些作用,表明内源性大麻素/内源性香草素系统参与了双氯芬酸的镇痛作用。