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一种内生真菌来源的氮杂菲酮通过抑制 MAPKs 和降低 Bax/Bcl-2 比值预防神经元细胞死亡。

Azaphilones from an Endophytic sp. Prevent Neuronal Cell Death via Inhibition of MAPKs and Reduction of Bax/Bcl-2 Ratio.

机构信息

College of Pharmacy, Duksung Women's University, Seoul 01369, Republic of Korea.

College of Korean Medicine, Gachon University, Seongnam 13120, Republic of Korea.

出版信息

J Nat Prod. 2021 Aug 27;84(8):2226-2237. doi: 10.1021/acs.jnatprod.1c00298. Epub 2021 Aug 11.

Abstract

Fourteen azaphilone-type polyketides (-), including nine new ones (- and -), were isolated from cultures of -associated sp. JVF17, and their structures were determined by spectroscopic analysis together with computational methods and chemical reactions. Neuroprotective effects of the isolated compounds were evaluated against glutamate-induced neurotoxicity. Treatment with compounds , , , and - increased cell viabilities of hippocampal neuronal cells damaged by glutamate, with compound being the most potent. Compound markedly decreased intracellular Ca and nuclear condensation levels. Mechanistically, molecular markers of apoptosis induced by treatment with glutamate, i.e., phosphorylation of MAPKs and elevated Bax/Bcl-2 expression ratio, were significantly lowered by compound . The azaphilones with an isoquinoline core structure were more active than those with pyranoquinones, but -substitution decreased the activity. This study, including the structure-activity relationship, indicates that the azaphilone scaffold is a promising lead toward the development of novel neuroprotective agents.

摘要

从与 - 相关的 - 中分离得到了 14 种氮杂菲酮型聚酮化合物(-),包括 9 种新化合物(- 和 -),并通过光谱分析以及计算方法和化学反应确定了它们的结构。评估了分离得到的化合物对谷氨酸诱导的神经毒性的神经保护作用。用化合物 、 、 、 和 - 处理受谷氨酸损伤的海马神经元细胞,可提高细胞活力,其中化合物 作用最强。化合物 可显著降低细胞内 Ca 和核浓缩水平。在机制上,用谷氨酸处理诱导的细胞凋亡的分子标记物,即 MAPKs 的磷酸化和 Bax/Bcl-2 表达比值的升高,均被化合物 显著降低。具有异喹啉核心结构的氮杂菲酮比具有吡喃并喹啉酮的化合物活性更高,但 - 取代会降低活性。这项包括构效关系的研究表明,氮杂菲酮支架是开发新型神经保护剂的有希望的先导化合物。

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