松露Picoa lefebvrei的真菌化学、抗氧化、细胞毒和酶抑制活性研究

IF 2.1 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Çiğdem Kuş , Meltem Taş Küçükaydın , Selçuk Küçükaydın , Mehmet Emin Duru , Mehmet Öztürk
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引用次数: 0

摘要

Picoa lefebvrei(帕特)麦尔松露是一种松露,属于松露科,菌根生长在菊花的根部。Picoa原产于西安纳托利亚和突尼斯,是人们首选的食物,具有经济潜力。近年来,人们对蘑菇的生物活性成分越来越感兴趣,食用蘑菇和一些松露被用于新一代的生物治疗药物。本研究通过不同的色谱方法,从P. lefebvrei提取物中分离得到8个化合物,分别为:油菜甾醇(1)、油菜甾醇-β-酰-氨基葡萄糖苷(2)、尿嘧啶(3)、l-尿苷(4)、赤藓糖醇(5)、α-酰-氨基葡萄糖苷(6)、油菜甾醇亚油酸酯(7)和5α-6α- 6α-环氧麦角糖-7,22-二烯-3β-醇(8)。此外,还对其提取物和化合物的抗氧化活性、抗胆碱酯酶活性、抗脲酶活性和细胞毒活性(对MCF-7、H1299和L929细胞系)进行了研究。化合物4在DPPH(2,2-二苯基-1-picrylhydrazyl)、ABTS (2,2 ' - azno -bis(3-乙基苯并噻唑-6-磺酸)和CUPRAC (cu离子还原抗氧化能力)试验中的IC50值分别为92.61±0.10、70.55±0.84和112.08±0.15µg/mL,显示出最高的抗氧化活性。化合物3和8对乙酰胆碱酯酶(AChE)(44.59±0.37%)和丁基胆碱酯酶(BChE)(53.15±1.07%)和54.97±0.41%)的抑制活性最高。化合物8对H1299肺癌细胞的细胞毒性最强,IC50值为33.94±0.47µg/mL。然而,化合物1 (IC50:24.72±0.75µg/mL)对MCF-7乳腺癌细胞表现出最大的细胞毒性。这些发现表明,P. lefebvrei富含甾体化合物,可能是麦角甾类类固醇的来源。此外,这项首次详细的调查强调了P. lefebvrei作为天然食品和生物活性化合物来源的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mycochemical investigation, antioxidant, cytotoxic and enzyme inhibition activities of truffle Picoa lefebvrei
Picoa lefebvrei (Pat.) Maire is a truffle species that belongs to the Cistaceae family and grows mycorrhizally on the roots of Helianthemum species. Picoa species, which is indigenous to Western Anatolia and Tunisia, have been preferred as food and have economic potential. Recently, interest in bioactive compounds of mushrooms has increased and it is known that edible mushrooms and some truffles are used in the new generation of biotherapeutics. In this report, eight compounds were isolated from P. lefebvrei extracts namely, brassicasterol (1), brassicasteryl-β-ᴅ-glucopyranoside (2), uracil (3), l-uridine (4), erythritol (5), α-ᴅ-glucopyranosyl-α-ᴅ-glucopyranoside (6), brassicasteryl linoleate (7) and 5α-6α-epoxy ergosta-7,22-diene-3β-ol (8) via various chromatographic methods. Also, antioxidant, anticholinesterase, anti-urease, and cytotoxic (against MCF-7, H1299 and L929 cell lines) activities of extracts and compounds from P. lefebvrei were investigated. Compound 4 exhibited the highest antioxidant activity with IC50 values of 92.61 ± 0.10, 70.55 ± 0.84 and 112.08 ± 0.15 µg/mL in the DPPH (2,2-Diphenyl-1-picrylhydrazyl), ABTS (2,2′-Azino-bis(3-ethylbenzothiazoline-6-sulfonic acid), and CUPRAC (Cupric Ion Reducing Antioxidant Capacity) assays, respectively. Compounds 3 and 8 exhibited the highest activities against acetylcholinesterase (AChE) (44.59 ± 0.37 % and 40.26 ± 0.53 %) and butyrylcholinesterase (BChE) (53.15 ± 1.07 % and 54.97 ± 0.41 %). Compound 8 had strongest cytotoxicity with IC50 value of 33.94 ± 0.47 µg/mL against the H1299 lung cancer cells. Nevertheless, compound 1 (IC50:24.72 ± 0.75 µg/mL), showed the greatest cytotoxicity against the MCF-7 breast cancer cells. These findings indicate that P. lefebvrei, is rich in steroidal compounds and is a possible source of ergostane-type steroids. Furthermore, this first detailed investigation highlights the potential of P. lefebvrei as a natural food and as a source of bioactive compounds.
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来源期刊
Steroids
Steroids 医学-内分泌学与代谢
CiteScore
5.10
自引率
3.70%
发文量
120
审稿时长
73 days
期刊介绍: STEROIDS is an international research journal devoted to studies on all chemical and biological aspects of steroidal moieties. The journal focuses on both experimental and theoretical studies on the biology, chemistry, biosynthesis, metabolism, molecular biology, physiology and pharmacology of steroids and other molecules that target or regulate steroid receptors. Manuscripts presenting clinical research related to steroids, steroid drug development, comparative endocrinology of steroid hormones, investigations on the mechanism of steroid action and steroid chemistry are all appropriate for submission for peer review. STEROIDS publishes both original research and timely reviews. For details concerning the preparation of manuscripts see Instructions to Authors, which is published in each issue of the journal.
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