斯里兰卡特有种树树的体外抗炎活性研究

S. Senadeera, K. Fernando, W. L. L. N. Wickramasekara, M. Fernando, C. Ranaweera, W. Rajapaksha, A. R. Silva
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引用次数: 4

摘要

目的:研究石竹水提液、甲醇提液、二氯甲烷提液和己烷提液的体外抗炎活性。叶和茎皮采用热诱导蛋白变性试验(蛋白蛋白变性)。方法:收集成熟、完全展开的鹿角树叶和茎皮各约500 g,清洗后风干。叶子和茎皮部分被磨碎以获得细粉末材料。采用煎提法提取。采用热诱导蛋清变性法评价其抗炎活性。双氯芬酸钠为阳性对照。结果:双氯芬酸钠对热致鸡蛋白蛋白变性试验的IC50值为243.4µg/mL,甲醇茎皮提取物对热致鸡蛋白蛋白变性试验的IC50值为249.8µg/mL。水提液、甲醇提液、二氯甲烷提液和己烷提液的R²和P值表明,各提液的浓度与百分抑制率之间存在显著的统计学相关性(P<0.01)。然而,甲醇茎皮提取物表现出最高的功效和效力,与阳性对照双氯芬酸钠的活性相似。结论:石竹茎皮甲醇提取物具有良好的药理作用。具有明显的体外抗炎活性。其抗炎作用机制及有效成分有待进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In vitro Anti-inflammatory Activity of Endemic Artocarpus nobilis Thw Found in Sri Lanka
Aims: To investigate in vitro anti-inflammatory activity of aqueous, methanol, dichloromethane, and hexane extracts of Artocarpus nobilis Thw. leaves and stem bark using heat-induced protein denaturation test (egg albumin denaturation). Methodology: About 500 g of each matured, fully expanded leaves and stem bark of Artocarpus nobilis were collected, washed and air-dried. Leaves and stem bark parts were grounded to obtain a fine powder material. The extractions were obtained using the decoction extraction method. Anti-inflammatory activity was evaluated using the heat-induced egg albumin denaturation method. Diclofenac sodium was used as the positive control. Results: Results showed that Diclofenac sodium exhibited an IC50 value of 243.4 µg/mL and methanolic stem bark extract had an IC50 Value of 249.8 µg/mL) for heat-induced egg albumin protein denaturation test. R² and P values for aqueous, methanol, dichloromethane, and hexane extracts indicated that there was a strong, statistically significant correlation (P<0.01) between concentration and percentage inhibition for all extracts of A. nobilis Thw. However, methanol stem bark extract demonstrated the highest efficacy and potency with similar activity observed for the positive control Diclofenac sodium. Conclusion: Methanol stem bark extract of Artocarpus nobilis Thw. have marked in vitro anti-inflammatory activity. Further studies are necessary to determine the mechanism and the active constituents responsible for the anti-inflammatory activity of the plant parts of Artocarpus nobilis Thw.
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