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Maria Eliza Castro Moreira,Rosemary Gualberto Fonseca Alvarenga Pereira,Marcelo Jose Dias Silva,Danielle Ferreira Dias,Vanessa Silva Gontijo,Alexandre Giusti-Paiva,Marcia Paranho Veloso,Antônio Carlos 한국식품영양과학회 2014 Journal of medicinal food Vol.17 No.6
In the present study, the pharmacological effects of 2,8-dihydroxy-1,6-dimethoxyxanthone from the bark of Haploclathra paniculata were investigated in mice using in vivo inflammation and nociception models. Acetic acid-induced writhing, paw licking induced by formalin, hot plate, and carrageenan-induced paw edema tests were used to investigate the antiinflammatory and antinociceptive activities of the xanthone compound. Xanthone, at both doses, inhibited abdominal writhing and the formalin test. At a dose of 20mg/kg, the time of reaction to the hot plate increased, and significant effects were observed after 30, 60 and 90min of treatment. At doses of 10 and 20mg/kg p.o., the 2,8-dihydroxy-1,6-dimethoxyxanthone significantly reduced paw edema at 3 h after the stimulus. The tests also showed no acute toxicity of the xanthone compound in mice. 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging ability was also studied and confirmed the antioxidant activity of the xanthone. To propose the mechanism of action of anti-inflammatory activity of the xanthone, a molecular docking was performed using the isoenzymes cyclooxygenase 1 and 2 and the results indicate that the molecule is capable of inhibiting both the enzymes. Therefore, it can be concluded that 2,8-dihydroxy-1,6-dimethoxyxanthone from H. paniculata demonstrates analgesic, anti-inflammatory, and antioxidant activities.