Mycochemical analysis, anti-inflammatory and cytotoxic activities of Pycnoporus sanguineus (L.) Murrill, a medicinal mushroom from Gabon

Juliette Ornely Orango Bourdette, Hugues Calixte Eyi Ndong, Henri Paul Bourobou Bourobou, Louis Clément Obame Engonga
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Abstract

A mycochemical study followed by an evaluation of anti-inflammatory and cytotoxic activities of Pycnoporus sanguineus, a species of lignicole mushroom exploited in traditional medicine in Gabon, was carried out on four extracts. Bioactive compounds were extracted by successive macerations with water, hydro-ethanol (50-50), ethanol solvents and sonication was used for dichloromethane-methanol (50-50) extraction. Agilent LC-MS system was used for the molecular profile of the different extracts and fractions. The fractionation of the extracts was made by flash chromatography and the purification using preparative chromatography. Structures of compounds responsible for the pharmacological activities were determinated by NMR. Cytotoxicity essay was carried out on PNT2 cells and the anticancer activities on A549 and PC3 cell lines. Two molecules have been isolated from this fungus; namely m/z 301.04 [M-H] + corresponding to cinnabarinic acid and m/z 287.06 [M-H]+ for which the NMR data were insufficient to confirm the molecular identification. Anti-inflammatory activity of the aqueous extract was stronger (IC50 = 197.82 μg/ml) than niflumic acid (IC50 = 809.27 μg/ml) but weaker than diclofenac (IC50 = 15.28 μg/ml). However, the hydro-ethanolic and ethanolic extracts of P. sanguineus, have a weaker anti-inflammatory activity than niflumic acid and diclofenac. About cytotoxicity, the crude extracts and fractions tested have anticancer and cytotoxic activities on A549, PC3 and PNT2 lines. However, these activities are more pronounced in the healthy line PNT2 than in the cancerous lines A549 and PC3.
血螺的真菌化学分析、抗炎和细胞毒活性来自加蓬的一种药用蘑菇
摘要对加蓬传统医药中开发的木脂素菌种——血螺(Pycnoporus sanguineus)的四种提取物进行了真菌化学研究,并对其抗炎和细胞毒活性进行了评价。采用水、氢乙醇(50-50)、乙醇溶剂和超声(50-50)连续浸渍法提取生物活性化合物。采用Agilent LC-MS系统对不同提取物和组分进行分子谱分析。采用闪蒸色谱法对提取物进行分离,制备色谱法对提取物进行纯化。通过核磁共振测定了化合物的药理活性。对PNT2细胞进行了细胞毒性试验,并对A549和PC3细胞株进行了抑癌活性试验。从这种真菌中分离出两个分子;即对应朱砂酸的m/z 301.04 [m - h]+和对应朱砂酸的m/z 287.06 [m - h]+,其核磁共振数据不足以确认分子鉴定。水提物的抗炎活性(IC50 = 197.82 μg/ml)高于尼氟酸(IC50 = 809.27 μg/ml),弱于双氯芬酸(IC50 = 15.28 μg/ml)。但其乙醇提取物和乙醇提取物的抗炎活性较尼氟酸和双氯芬酸弱。细胞毒性方面,对A549、PC3和PNT2细胞系均有抑癌和细胞毒性作用。然而,这些活性在健康细胞系PNT2中比在癌变细胞系A549和PC3中更为明显。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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