Chemical Composition, Antioxidant and Anti-Inflammatory Activity of Shiitake Mushrooms (Lentinus edodes)

被引:1
|
作者
Xu, Xiaoming [1 ]
Yu, Chong [1 ,2 ]
Liu, Zhenyang [3 ]
Cui, Xiaohang [1 ]
Guo, Xiaohe [1 ]
Wang, Haifeng [1 ,2 ,4 ]
机构
[1] Shenyang Pharmaceut Univ, Sch Tradit Chinese Mat Med, Minist Educ, Key Lab Struct Based Drug Design & Discovery, Shenyang 110016, Peoples R China
[2] Guangxi Acad Sci, Guangxi Key Lab Marine Nat Prod & Combinatorial Bi, Nanning 530007, Peoples R China
[3] Shenyang Baide Biotechnol Co Ltd, Shenyang 110016, Peoples R China
[4] Shenyang Pharmaceut Univ, Sch Tradit Chinese Mat Med, Key Lab Innovat Tradit Chinese Med Major Chron Dis, Shenyang 110016, Peoples R China
关键词
shiitake mushroom (Lentinus edodes); edible fungi; mycelium and fruiting body; bioactive compounds; anti-inflammatory activity; antioxidant activity; TNF-ALPHA; NITRITE;
D O I
10.3390/jof10080552
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Shiitake mushrooms (Lentinus edodes) are renowned as the "King of mountain treasures" in China due to their abundant nutritional and health-enhancing properties. Intensive chemical investigations of the fruiting bodies and mycelium of Shiitake mushrooms (Lentinus edodes) afforded five new compounds (1-5), named lentinmacrocycles A-C and lentincoumarins A-B, along with fifteen known compounds (6-20). Their structures and absolute configurations were elucidated by extensive spectroscopic analysis, including one-and two-dimensional (1D and 2D) NMR spectroscopy, circular dichroism (CD), and high-resolution electrospray ionization mass spectrometry (HR-ESI-MS). The anti-inflammatory activity test showed that lentincoumarins A (4), (3S)-7-hydroxymellein (9), (3R)-6-hydroxymellein (11) and succinic acid (18) exhibited strong NO inhibitory effects (IC50 < 35 mu M), and that (3S)-5-hydroxymellein (10) and (3R)-6-hydroxymellein (11) exhibited potent TNF-alpha inhibitory effects (IC50 < 80 mu M) and were more potent than the positive control, Indomethacin (IC50 = 88.5 +/- 2.1 mu M). The antioxidant activity test showed that (3R)-6-hydroxymellein (11) had better DPPH radical scavenging activity (IC50 = 25.2 +/- 0.5 mu M).
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页数:13
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