Abstract
Here we investigated the anti-inflammatory properties of Ocotea quixos essential oil and of its main components, trans-cinnamaldehyde and methyl cinnamate, in in vitro and in vivo models. Ocotea essential oil and trans-cinnamaldehyde but not methyl cinnamate significantly reduced LPS-induced NO release from J774 macrophages at non-toxic concentrations, inhibited LPS-induced COX-2 expression and increased forskolin-induced cAMP production. The essential oil (30-100mg/kg os) and trans-cinnamaldehyde (10mg/kg os) in carrageenan-induced rat paw edema showed anti-inflammatory effect without damaging gastric mucosa. In conclusion we provide the first evidence of a significant anti-inflammatory gastro-sparing activity of O.quixos essential oil.
(c) 2009 Elsevier B.V. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Acrolein / analogs & derivatives*
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Acrolein / isolation & purification
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Acrolein / pharmacology
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Acrolein / therapeutic use
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Animals
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Anti-Inflammatory Agents / isolation & purification
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Anti-Inflammatory Agents / pharmacology
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Anti-Inflammatory Agents / therapeutic use*
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Antineoplastic Agents, Phytogenic / isolation & purification
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Antineoplastic Agents, Phytogenic / pharmacology
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Antineoplastic Agents, Phytogenic / therapeutic use
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Carrageenan
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Cell Line, Tumor
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Cinnamates
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Edema / chemically induced
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Edema / drug therapy*
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Gastric Mucosa / drug effects
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Humans
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Inflammation Mediators / metabolism*
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Lipopolysaccharides
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Macrophages / drug effects
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Male
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Neuroblastoma / drug therapy
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Ocotea / chemistry*
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Oils, Volatile / chemistry
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Oils, Volatile / pharmacology
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Oils, Volatile / therapeutic use*
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Phytotherapy
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Plant Extracts / chemistry
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Plant Extracts / pharmacology
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Plant Extracts / therapeutic use*
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Rats
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Rats, Wistar
Substances
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Anti-Inflammatory Agents
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Antineoplastic Agents, Phytogenic
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Cinnamates
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Inflammation Mediators
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Lipopolysaccharides
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Oils, Volatile
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Plant Extracts
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methyl cinnamate
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Acrolein
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Carrageenan
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cinnamaldehyde