Anti-inflammatory activity, cytotoxicity and active compounds of Tinospora smilacina Benth.

被引:37
作者
Li, RW
Leach, DN
Myers, SP
Leach, GJ
Lin, GD
Brushett, DJ
Waterman, PG
机构
[1] Univ Hawaii Manoa, John A Burns Sch Med, Med Technol Div, Honolulu, HI 96822 USA
[2] So Cross Univ, Ctr Phytochem, Lismore, NSW, Australia
[3] Univ Queensland, Australian Ctr Complementary Med Educ & Res, St Lucia, Qld 4067, Australia
[4] Pks & Wildlife Commis No Territory, Palmerston, NT, Australia
关键词
anti-inflammatory activity; cycloxygenase-1; and-2; 5-lipoxygenase; Tinospora smilacina; cytotoxicity; LC-MS; NMR;
D O I
10.1002/ptr.1373
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Tinospora smilacina Benth. has been used in Australian indigenous medicine for the treatment of headache, rheumatoid arthritis and other inflammatory disorders. As part of an investigation into the anti-inflammatory potential of plants using an ethnopharmacological approach, the present study sought to evaluate the efficacy and safety of Tinospora smilacina. An ethanol extract of this plant was evaluated in vitro for anti-inflammatory activities on cyclooxygenase-1(COX-1), cyclooxygenase-2 (COX-2), 5-lipoxygenase (5-LO) and phospholipase A(2) (PA(2)). The ethanol extract of Tinospora smilacina showed inhibitory activities on COX-1, COX-2, 5-LO and PA(2) with the IC50 values of 63.5, 81.2, 92.1 and 30.5 mug/mL respectively. Cytotoxic effect of the extracts of Tinospora smilacina was investigated in vitro using ATP-based luminescence assay and the results showed no cytotoxic effect on cell lines of skin fibroblasts (1BR3), human Caucasian hepatocyte carcinoma (Hep G2) and human Caucasian promyelocytic leukaemia (HL-60). This paper also describes the results of fractionations and bioassay guided chemical studies, suggesting that the anti-inflammatory activity is due to triterpene-fatty acid esters and free fatty acids. Copyright (C) 2004 John Wiley Sons, Ltd.
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页码:78 / 83
页数:6
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