Comparative evaluation of the pain-relieving properties of a lecithinized formulation of curcumin (Meriva®), nimesulide, and acetaminophen

Francesco Di Pierro,1 Giuliana Rapacioli,2 Eleonora Adriana Di Maio,3 Giovanni Appendino,4 Federico Franceschi,5 Stefano Togni5 1Velleja Research, 2Associazione Italiana Omeopatia di Risonanza, 3Presidio Ospedaliero Riunito Ciriè-Lanzo, 4Università degli Studi del Piemo...

Full description

Bibliographic Details
Main Authors: Di Pierro F, Rapacioli G, Di Maio EA, Appendino G, Franceschi F, Togni S
Format: Article
Language:English
Published: Dove Medical Press 2013-03-01
Series:Journal of Pain Research
Online Access:http://www.dovepress.com/comparative-evaluation-of-the-pain-relieving-properties-of-a-lecithini-a12404
_version_ 1819136455674429440
author Di Pierro F
Rapacioli G
Di Maio EA
Appendino G
Franceschi F
Togni S
author_facet Di Pierro F
Rapacioli G
Di Maio EA
Appendino G
Franceschi F
Togni S
author_sort Di Pierro F
collection DOAJ
description Francesco Di Pierro,1 Giuliana Rapacioli,2 Eleonora Adriana Di Maio,3 Giovanni Appendino,4 Federico Franceschi,5 Stefano Togni5 1Velleja Research, 2Associazione Italiana Omeopatia di Risonanza, 3Presidio Ospedaliero Riunito Ciriè-Lanzo, 4Università degli Studi del Piemonte Orientale, 5Indena SpA, Milan, Italy Abstract: In addition to its anti-inflammatory activity, Meriva®, a proprietary lecithin formulation of curcumin, has been anecdotally reported to decrease acute pain in patients with various chronic diseases. Given that curcumin can desensitize transient receptor potential A1, a nociceptor seemingly also mediating the analgesic effect of acetaminophen, as well as inhibiting and downregulating the expression of cyclo-oxygenase 2, the selective target of nimesulide, a nonsteroidal anti-inflammatory agent, we carried out a pilot comparative study of the acute pain-relieving properties of these three agents. At a dose of 2 g (corresponding to 400 mg of curcumin), Meriva showed clear analgesic activity, comparable with that of a standard dose (1 g) of acetaminophen, but lower than that of a therapeutic (100 mg) dose of nimesulide. The analgesic activity of lower (1.5 g) doses of Meriva was less satisfactory, and the onset of activity was longer than that of nimesulide for both doses. On the other hand, gastric tolerability was significantly better than that of nimesulide and comparable with that of acetaminophen. Taken together, our results show that the preclinical analgesic properties of curcumin have clinical relevance, at least at a dose of 2 g as the Meriva formulation. While this dose is significantly higher than that used to relieve chronic inflammatory conditions (1–1.2 g/day), its pain-relieving activity could benefit from the general downregulation of the inflammatory response induced by curcumin, considering that the transient receptor potential channel-mediated mechanisms of analgesia are magnified by attenuation of inflammation. In patients on treatment with Meriva, this would also translate into better control of acute pain, providing a rationale for the analgesic properties associated with this curcumin formulation. Keywords: curcumin phytosome, Meriva®, acute pain, acetaminophen, nimesulide, tolerability
first_indexed 2024-12-22T10:35:15Z
format Article
id doaj.art-6e91bf78cce549538bcf876bfc98d5c3
institution Directory Open Access Journal
issn 1178-7090
language English
last_indexed 2024-12-22T10:35:15Z
publishDate 2013-03-01
publisher Dove Medical Press
record_format Article
series Journal of Pain Research
spelling doaj.art-6e91bf78cce549538bcf876bfc98d5c32022-12-21T18:29:12ZengDove Medical PressJournal of Pain Research1178-70902013-03-012013default201205Comparative evaluation of the pain-relieving properties of a lecithinized formulation of curcumin (Meriva®), nimesulide, and acetaminophenDi Pierro FRapacioli GDi Maio EAAppendino GFranceschi FTogni SFrancesco Di Pierro,1 Giuliana Rapacioli,2 Eleonora Adriana Di Maio,3 Giovanni Appendino,4 Federico Franceschi,5 Stefano Togni5 1Velleja Research, 2Associazione Italiana Omeopatia di Risonanza, 3Presidio Ospedaliero Riunito Ciriè-Lanzo, 4Università degli Studi del Piemonte Orientale, 5Indena SpA, Milan, Italy Abstract: In addition to its anti-inflammatory activity, Meriva®, a proprietary lecithin formulation of curcumin, has been anecdotally reported to decrease acute pain in patients with various chronic diseases. Given that curcumin can desensitize transient receptor potential A1, a nociceptor seemingly also mediating the analgesic effect of acetaminophen, as well as inhibiting and downregulating the expression of cyclo-oxygenase 2, the selective target of nimesulide, a nonsteroidal anti-inflammatory agent, we carried out a pilot comparative study of the acute pain-relieving properties of these three agents. At a dose of 2 g (corresponding to 400 mg of curcumin), Meriva showed clear analgesic activity, comparable with that of a standard dose (1 g) of acetaminophen, but lower than that of a therapeutic (100 mg) dose of nimesulide. The analgesic activity of lower (1.5 g) doses of Meriva was less satisfactory, and the onset of activity was longer than that of nimesulide for both doses. On the other hand, gastric tolerability was significantly better than that of nimesulide and comparable with that of acetaminophen. Taken together, our results show that the preclinical analgesic properties of curcumin have clinical relevance, at least at a dose of 2 g as the Meriva formulation. While this dose is significantly higher than that used to relieve chronic inflammatory conditions (1–1.2 g/day), its pain-relieving activity could benefit from the general downregulation of the inflammatory response induced by curcumin, considering that the transient receptor potential channel-mediated mechanisms of analgesia are magnified by attenuation of inflammation. In patients on treatment with Meriva, this would also translate into better control of acute pain, providing a rationale for the analgesic properties associated with this curcumin formulation. Keywords: curcumin phytosome, Meriva®, acute pain, acetaminophen, nimesulide, tolerabilityhttp://www.dovepress.com/comparative-evaluation-of-the-pain-relieving-properties-of-a-lecithini-a12404
spellingShingle Di Pierro F
Rapacioli G
Di Maio EA
Appendino G
Franceschi F
Togni S
Comparative evaluation of the pain-relieving properties of a lecithinized formulation of curcumin (Meriva®), nimesulide, and acetaminophen
Journal of Pain Research
title Comparative evaluation of the pain-relieving properties of a lecithinized formulation of curcumin (Meriva®), nimesulide, and acetaminophen
title_full Comparative evaluation of the pain-relieving properties of a lecithinized formulation of curcumin (Meriva®), nimesulide, and acetaminophen
title_fullStr Comparative evaluation of the pain-relieving properties of a lecithinized formulation of curcumin (Meriva®), nimesulide, and acetaminophen
title_full_unstemmed Comparative evaluation of the pain-relieving properties of a lecithinized formulation of curcumin (Meriva®), nimesulide, and acetaminophen
title_short Comparative evaluation of the pain-relieving properties of a lecithinized formulation of curcumin (Meriva®), nimesulide, and acetaminophen
title_sort comparative evaluation of the pain relieving properties of a lecithinized formulation of curcumin meriva amp reg nimesulide and acetaminophen
url http://www.dovepress.com/comparative-evaluation-of-the-pain-relieving-properties-of-a-lecithini-a12404
work_keys_str_mv AT dipierrof comparativeevaluationofthepainrelievingpropertiesofalecithinizedformulationofcurcuminmerivaampregnimesulideandacetaminophen
AT rapaciolig comparativeevaluationofthepainrelievingpropertiesofalecithinizedformulationofcurcuminmerivaampregnimesulideandacetaminophen
AT dimaioea comparativeevaluationofthepainrelievingpropertiesofalecithinizedformulationofcurcuminmerivaampregnimesulideandacetaminophen
AT appendinog comparativeevaluationofthepainrelievingpropertiesofalecithinizedformulationofcurcuminmerivaampregnimesulideandacetaminophen
AT franceschif comparativeevaluationofthepainrelievingpropertiesofalecithinizedformulationofcurcuminmerivaampregnimesulideandacetaminophen
AT tognis comparativeevaluationofthepainrelievingpropertiesofalecithinizedformulationofcurcuminmerivaampregnimesulideandacetaminophen