2011
DOI: 10.1007/s11418-011-0517-y
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Antinociceptive effect of Lafoensia pacari A. St.-Hil. independent of anti-inflammatory activity of ellagic acid

Abstract: This study was performed to determine the antinociceptive and anti-inflammatory activities of ethanolic extract of Lafoensia pacari A. St.-Hil. (PEtExt) stem bark and its fractions using various animal models such as acetic acid-induced abdominal writhing, formalin-induced pain and croton oil-induced ear edema tests. The PEtExt inhibited the acetic acid-induced abdominal writhing, reduced the pain reaction time on both phases of the formalin test and decreased the edema in a dose-dependent manner. Pre-treatmen… Show more

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Cited by 19 publications
(13 citation statements)
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References 37 publications
(43 reference statements)
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“…In fact, the broad community access to Amazon or Pantanal biome, and the close relationship with the indigenous native populations, promotes a variety of possibilities of ethnobotanical indications. Examples of other popular uses of L. pacari that have been experimentally confirmed includes weight loss [145], anorectic effect [142], antipyretic activity [146], anti-inflammatory [147], antiallergic [148], and analgesic property [149]. …”
Section: Discussionmentioning
confidence: 99%
“…In fact, the broad community access to Amazon or Pantanal biome, and the close relationship with the indigenous native populations, promotes a variety of possibilities of ethnobotanical indications. Examples of other popular uses of L. pacari that have been experimentally confirmed includes weight loss [145], anorectic effect [142], antipyretic activity [146], anti-inflammatory [147], antiallergic [148], and analgesic property [149]. …”
Section: Discussionmentioning
confidence: 99%
“…On the other hand, the high dose bufalin (0.6 mg/kg) inhibited both phases of the formalin test, but its effect was more pronounced in the inflammatory phase. This result suggested that a high dose of bufalin also modulates acute neurogenic pain, which is sensitive to drugs with a central action [26, 27, 30]. …”
Section: Discussionmentioning
confidence: 99%
“…EA has been reported to be effective as an antinociceptive compound in several nociceptive assays. [111221] Moreover, in our previous work, we demonstrated the participation of both central and peripheral antinociception induced by EA in several pain models, which was mediated through opioidergic and NO-cGMP pathways. [13]…”
Section: Discussionmentioning
confidence: 99%
“…[11] Moreover, Corbett et al ., (2010) showed that EA decreases paw edema induced by 3% carrageenan and may interact with ketorolac as a potent inhibitor of COX enzyme. [12] In a previous study, we demonstrated that EA produces antinociceptive effects in different experimental models of nociception via the opioidergic and NO-cGMP pathways in different animal models of pain.…”
Section: Introductionmentioning
confidence: 99%