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从可食用蘑菇粗糙红菇(Santi)Pouzar 中分离和阐明细胞毒性麦角甾烷的研究进展。

Insight into isolation and elucidation of cytotoxic ergostanoids from the mushroom Sarcosphaera crassa (Santi) Pouzar: An edible mushroom.

机构信息

Department of Chemistry, Faculty of Sciences, Muğla Sıtkı Koçman University, 48121 Kötekli, Muğla Turkey.

Department of Pharmacognosy, Faculty of Pharmacy, Dicle University, 21280 Diyarbakir, Turkey.

出版信息

Steroids. 2022 May;181:108990. doi: 10.1016/j.steroids.2022.108990. Epub 2022 Feb 23.

Abstract

Sarcosphaera crassa is a mushroom consumed in Europe and Anatolia after being cooked well. The cytotoxic activity of the extracts of unbaked S. crassa against MCF7, HT29, HeLa cancer cell lines and toxicity against PDF fibroblast healthy cell lines were studied using MTT assay. Acetone and methanol extracts of the mushroom exhibited significant cytotoxic activity. Further investigation of cytotoxic extracts afforded two new fatty acid sterols (1-2), a new ergosterol glycoside (4), and seven known compounds, including a fatty acid sterol (3), a steroid glycoside (5), two ergostanoids (6-7) and three sugars (8-10). These compounds were identified as brassicasteryl heptadecanoate (1), brassicasteryl palmitoleate (2), brassicasteryl linoleate (3), brassicasterol β-ᴅ-xylofuranoside (4), brassicasterol β-ᴅ-glucoside (5), brassicasterol (6), ergosterol-endoperoxide (7), mannitol (8), erythritol (9) and turanose (10). Among them, 7 exhibited a moderate cytotoxic activity against HeLa (IC: 70.1 ± 2.0 µg/mL) and high activity against HT29 (IC: 38.8 ± 0.9 µg/mL), and MCF7 (IC: 62.9 ± 1.3 µg/mL) cancer cell lines. Compounds 4, 5, and 6 also exhibited significant cytotoxic activity against HT29 and MCF7. Moreover, all compounds exhibited weak toxicity against PDF healthy cell lines. This study indicates the potential use of Sarcosphaera crassa as a natural source of cytotoxic ergostanoids, which can be considered a dietary supplement for cancer prevention.

摘要

糙皮侧耳是一种在欧洲和安纳托利亚食用的蘑菇,需要经过充分烹饪。使用 MTT 测定法研究了未烘焙糙皮侧耳提取物对 MCF7、HT29、HeLa 癌细胞系的细胞毒性活性和对 PDF 成纤维细胞健康细胞系的毒性。丙酮和甲醇提取物表现出显著的细胞毒性活性。对细胞毒性提取物的进一步研究提供了两种新的脂肪酸甾醇(1-2)、一种新的麦角甾醇糖苷(4)和七种已知化合物,包括一种脂肪酸甾醇(3)、一种甾体糖苷(5)、两种麦角甾烷(6-7)和三种糖(8-10)。这些化合物被鉴定为菜籽油甾醇十七烷酸酯(1)、菜籽油甾醇棕榈油酸酯(2)、菜籽油甾醇亚油酸酯(3)、菜籽油甾醇β-D-吡喃木糖苷(4)、菜籽油甾醇β-D-葡萄糖苷(5)、菜籽油甾醇(6)、麦角甾醇过氧化物(7)、甘露醇(8)、赤藓糖醇(9)和塔罗糖(10)。其中,化合物 7 对 HeLa(IC:70.1±2.0µg/mL)具有中等细胞毒性活性,对 HT29(IC:38.8±0.9µg/mL)和 MCF7(IC:62.9±1.3µg/mL)癌细胞系具有高活性。化合物 4、5 和 6 对 HT29 和 MCF7 也表现出显著的细胞毒性活性。此外,所有化合物对 PDF 健康细胞系均表现出较弱的毒性。本研究表明糙皮侧耳可作为细胞毒性麦角甾烷的天然来源,可作为预防癌症的膳食补充剂。

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