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Neuroprotective and antidiabetic lanostane-type triterpenoids from the fruiting bodies of Ganoderma theaecolum

文献类型: 外文期刊

作者: Guo, Jiaocen 1 ; Yang, Li 2 ; Dai, Luting 2 ; Ma, Qingyun 2 ; Yan, Jiaoyang 1 ; Xie, Qingyi 2 ; Wu, Yougen 1 ; Dai, Haofu 2 ; Zhao, Youxing 2 ;

作者机构: 1.Hainan Univ, Sanya Inst Breeding & Multiplicat, Sch Breeding & Multiplicat, Sanya 572025, Peoples R China

2.Chinese Acad Trop Agr Sci, Inst Trop Biosci & Biotechnol, Key Lab Res & Dev Nat Prod Li Folk Med Hainan Prov, Haikou 571101, Peoples R China

3.Chinese Acad Trop Agr Sci, Inst Trop Biosci & Biotechnol, Natl Key Lab Trop Crop Breeding, Haikou 571101, Peoples R China

关键词: Ganoderma theaecolum; Lanostane nortriterpenoids; Neuroprotective effects; PTP1B; alpha-Glucosidase

期刊名称:CHINESE JOURNAL OF NATURAL MEDICINES ( 影响因子:4.9; 五年影响因子:4.8 )

ISSN: 2095-6975

年卷期: 2025 年 23 卷 2 期

页码:

收录情况: SCI

摘要: Eight previously undescribed lanostane triterpenoids, including five nortriterpenoids with 26 carbons, ganothenoids A-E (1-5), and three lanostanoids, ganothenoids F-H (6-8), along with 24 known ones (9-32), were isolated from the fruiting bodies of Ganodrma theaecolum. The structures of the novel compounds were elucidated using comprehensive spectroscopic methods, including electronic circular dichroism (ECD) and nuclear magnetic resonance (NMR) calculations. Compounds 1-32 were assessed for their neuroprotective effects against H2O2-induced damage in human neuroblastoma SH-SY5Y cells, as well as their inhibitory activities against protein tyrosine phosphatase 1B (PTP1B) and alpha-glucosidase. Compound 4 demonstrated the most potent neuroprotective activity against H2O2-induced oxidative stress by suppressing G0/G1 phase cell cycle arrest, reducing reactive oxygen species (ROS) levels, and inhibiting cell apoptosis through modulation of B-cell lymphoma 2 protein (Bcl-2) and Bcl2 associated X-protein (Bax) protein expression. Compounds 26, 12, and 28 exhibited PTP1B inhibitory activities with IC50 values ranging from 13.92 to 56.94 mu molL-1, while compound 12 alone displayed significant inhibitory effects on alpha-glucosidase with an IC50 value of 43.56 mu molL-1. Additionally, enzyme kinetic analyses and molecular docking simulations were conducted for compounds 26 and 12 with PTP1B and alpha-glucosidase, respectively.

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