Physalis angulata extract exerts anti-inflammatory effects in rats by inhibiting different pathways
Physalis angulata is a popular medicine used in Brazil due to its anti-inflammatory effects, but the pharmacological mechanisms underlying these actions remain to be better understood. In the present work, lyophilized aqueous extract from the roots of Physalis angulata Linneu (AEPa) was used to cont...
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Veröffentlicht in: | Journal of ethnopharmacology 2008-07, Vol.118 (2), p.246-251 |
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Sprache: | eng |
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Zusammenfassung: | Physalis angulata is a popular medicine used in Brazil due to its anti-inflammatory effects, but the pharmacological mechanisms underlying these actions remain to be better understood. In the present work, lyophilized aqueous extract from the roots of
Physalis angulata Linneu (AEPa) was used to control the inflammatory response induced by the injection of 1% carrageenan into subcutaneous rat's air pouches. Adenosine deaminase (ADA) activity, nitrite level, and prostaglandin E
2 (PGE
2) level were used to evaluate the action of inflammatory mediators. Tumor growth factor-β (TGF-β) level was used as a bioindicator of immunomodulatory response. Rats were injected with vehicle, indomethacin, or AEPa (0.5
mg/kg, 1
mg/kg, and 5
mg/kg i.p.), 1
h before carrageenan administration. AEPa at 0.5
mg/kg had no effect. However, 1
mg/kg of AEPa showed significant anti-inflammatory effects, decreasing exudate volume, total number of inflammatory cells, ADA activity, nitrite level, and PGE
2 level in 50%, 41%, 20%, 60%, and 41%, respectively. The anti-inflammatory effects of 5
mg/kg AEPa appeared to be more effective than those of 1
mg/kg AEPa (84%, 80%, 43%, 70%, and 75%, respectively). In addition, TGF-β level was upregulated to 9700
pg/ml after 5
mg/kg AEPa, in comparison with 160
pg/ml in the vehicle-treated group, and 137
pg/ml in the indomethacin-treated group. The results indicate that AEPa exerts powerful anti-inflammatory and immunomodulatory activities, interfering with the cyclooxygenase pathway, lymphocyte proliferation, NO, and TGF-β production. |
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ISSN: | 0378-8741 1872-7573 |
DOI: | 10.1016/j.jep.2008.04.005 |