Zhang Jiao-Jiao, Wang Dai-Wei, Cai Dan, Lu Qing, Cheng Yong-Xian
Institute for Inheritance-Based Innovation of Chinese Medicine, School of Pharmaceutical Sciences, Health Science Center, Shenzhen University, Shenzhen, China.
Institute of Microscale Optoelectronics, Shenzhen University, Shenzhen, China.
Front Chem. 2021 Nov 3;9:772740. doi: 10.3389/fchem.2021.772740. eCollection 2021.
fungi as popular raw materials of numerous functional foods have been extensively investigated. In this study, five pairs of meroterpenoid enantiomers beyond well-known triterpenoids and polysaccharides, dayaolingzhiols I-M (-), were characterized from Their structures were identified using spectroscopic and computational methods. Structurally, compound features a novel dioxabicyclo[2.2.2]octan-3-one motif in the side chain. Ethnoknowledge-derived biological evaluation found that (+)- could activate Akt and AMPK phosphorylation in insulin-stimulated C2C12 cells, and (+)- could activate glucose uptake dose dependently in C2C12 cells. Furthermore, we found that (+)- (+)-, and (-)- could significantly inhibit cell migration of the MDA-MB-231 cell line, of which (+)- showed significant inhibitory effects against cell migration of the MDA-MB-231 cell line in a dose-dependent manner. These findings revealed the meroterpenoidal composition of and its roles in the prevention of chronic diseases such as diabetes mellitus and triple-negative breast cancer.
真菌作为众多功能性食品的常用原料已得到广泛研究。在本研究中,从[具体来源未给出]中鉴定出了五对除了著名的三萜类化合物和多糖之外的杂萜对映体,即大瑶灵芝醇I - M(-)。使用光谱和计算方法确定了它们的结构。在结构上,化合物在侧链中具有一个新颖的二氧杂双环[2.2.2]辛烷 - 3 - 酮基序。基于民族知识的生物学评估发现,(+) - [具体化合物未明确]可在胰岛素刺激的C2C12细胞中激活Akt和AMPK磷酸化,并且(+) - [具体化合物未明确]可在C2C12细胞中剂量依赖性地激活葡萄糖摄取。此外,我们发现(+) - [具体化合物未明确]、(+) - [具体化合物未明确]和( - ) - [具体化合物未明确]可显著抑制MDA - MB - 231细胞系的细胞迁移,其中(+) - [具体化合物未明确]对MDA - MB - 231细胞系的细胞迁移表现出显著的剂量依赖性抑制作用。这些发现揭示了[具体来源未给出]的杂萜类成分及其在预防糖尿病和三阴性乳腺癌等慢性疾病中的作用。