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. 2012:2012:138954.
doi: 10.1155/2012/138954. Epub 2012 Dec 29.

Analgesic and Anti-Inflammatory Activities of the Ethanolic Extract of Artemisia morrisonensis Hayata in Mice

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Analgesic and Anti-Inflammatory Activities of the Ethanolic Extract of Artemisia morrisonensis Hayata in Mice

Shen-Chieh Chou et al. Evid Based Complement Alternat Med. 2012.

Abstract

The aim of this study was to investigate the possible analgesic and anti-inflammatory mechanisms of the ethanolic extract of A. morrisonensis Hayata (AM(EtOH)). Two models were employed for evaluation of the analgesic effects: acetic acid-induced writhing response and formalin-induced paw licking. The results demonstrated that AM(EtOH) decreased writhing response for both the acetic acid assay and the licking time in the formalin test. The anti-inflammatory effect was evaluated by paw edema of mice induced by λ-carrageenan. AM(EtOH) significantly decreased induced paw edema three to four hours after λ-carrageenan injection. Additionally, the results indicated that the anti-inflammatory mechanism of AM(EtOH) may be due to the declined levels of nitric oxide (NO) and malondialdehyde (MDA) in the edematous paw. Furthermore, AM(EtOH) decreased the tumor necrosis factor-alpha (TNF-α) and interleukin-6 (IL-6) levels, leading to the reduction of prostaglandins and subsequently alleviated edema. Isolation and purification of the AM(EtOH) extract determined p-hydroxyacetophenone to be a major component at 130 mg/g of extract. No mortality was observed in the acute toxicity test given at the dose of 10 g/kg. This study demonstrated the possible mechanisms for the analgesic and anti-inflammatory effects of AM(EtOH) for mice and provided evidence for the ethnobotanical uses of A. morrisonensis in treating inflammatory diseases.

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Figures

Figure 1
Figure 1
(a) Base peak chromatogram (BPC) from LC-MS of AMEtOH. (b) Extracted ion chromatogram (EIC) from m/z 134.9 of AMEtOH; fragment ions were shown as insert. (c) BPC of authentic p-hydroxyacetophenone; fragment ions were shown as insert. All chromatograms were detected in the negative ion mode.
Figure 2
Figure 2
HPLC chromatogram of AMEtOH detected at 315 nm; p-hydroxyacetophenone is identified at RT = 15.99 min.
Figure 3
Figure 3
Analgesic effects of ethanol extract of AMEtOH and indomethacin (Indo) on acetic acid-induced writhing response in mice. Each value represents as mean ± SEM (n = 10), *P < 0.05, ***P < 0.001 as compared with the control (Con) group. (One-way ANOVA followed by Scheffe's multiple range test.)
Figure 4
Figure 4
Analgesic effects of AMEtOH and indomethacin (Indo) on the (a) early phase and (b) late phase in formalin test in mice. Each value represents as mean ± S.E.M. (n = 10), **P < 0.01, ***P < 0.001 as compared with the control (Con) group. (One-way ANOVA followed by Scheffe's multiple range test.)
Figure 5
Figure 5
Effects of AMEtOH and indomethacin (Indo) on hind paw edema induced by λ-carrageenan in mice. Each value represents as mean ± S.E.M. (n = 10), ***P < 0.001 as compared with the λ-carrageenan (Carr) group. (One-way ANOVA followed by Scheffe's multiple range test.)
Figure 6
Figure 6
Effects of AMEtOH and indomethacin (Indo) on the tissue COX-2 concentration of edema paw in mice. Each value represents as mean ± S.E.M. (n = 10), **P < 0.01, ***P < 0.001 as compared with the Carr group. (One-way ANOVA followed by Scheffe's multiple range test.)
Figure 7
Figure 7
Effects of AMEtOH and indomethacin (Indo) on the tissue TNF-α concentration of edema paw in mice. Each value represents as means ± SEM (n = 10), *P < 0.05, ***P < 0.001 as compared with the Carr group. (One-way ANOVA followed by Scheffe's multiple range test.)
Figure 8
Figure 8
Effects of AMEtOH and indomethacin (Indo) on the tissue IL-6 concentration of edema paw in mice. Each value represents as means ± SEM (n = 10), *P < 0.05 as compared with the Carr group. (One-way ANOVA followed by Scheffe's multiple range test.)
Figure 9
Figure 9
Effects of AMEtOH and indomethacin (Indo) on the tissue NO concentration of edema paw in mice. Each value represents as mean ± S.E.M. (n = 10), **P < 0.01, ***P < 0.001 as compared with the Carr group. (One-way ANOVA followed by Scheffe's multiple range test.)
Figure 10
Figure 10
Effects of AMEtOH and indomethacin (Indo) on the tissue MDA concentration of edema paw in mice. Each value represents as mean ± S.E.M. (n = 10), **P < 0.01, ***P < 0.001 as compared with the Carr group. (One-way ANOVA followed by Scheffe's multiple range test.)
Figure 11
Figure 11
Effects of AMEtOH and indomethacin (Indo) on the liver SOD activities in mice. Each value represents as mean ± SEM (n = 10), **P < 0.01, ***P < 0.001 as compared with the Carr group. (One-way ANOVA followed by Scheffe's multiple range test.)
Figure 12
Figure 12
Effects of AMEtOH and indomethacin (Indo) on the liver GPx activities in mice. Each value represents as mean ± SEM (n = 10), **P < 0.01, ***P < 0.001 as compared with the Carr group. (One-way ANOVA followed by Scheffe's multiple range test.)
Figure 13
Figure 13
Effects of AMEtOH and indomethacin (Indo) on the liver GRd activities in mice. Each value represents as mean ± S.E.M. (n = 10), **P < 0.01, ***P < 0.001 as compared with the Carr group. (One-way ANOVA followed by Scheffe's multiple range test.)

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