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来自[具体来源未提及]的多酚化合物可保护神经元细胞免受氧化应激。

Polyphenolic Compounds from Protect Neuronal Cells from Oxidative Stress.

作者信息

Tarbeeva Darya V, Pislyagin Evgeny A, Menchinskaya Ekaterina S, Berdyshev Dmitrii V, Kalinovskiy Anatoliy I, Grigorchuk Valeria P, Mishchenko Natalia P, Aminin Dmitry L, Fedoreyev Sergey A

机构信息

G.B. Elyakov Pacific Institute of Bioorganic Chemistry, Far Eastern Branch, Russian Academy of Science, 690022 Vladivostok, Russia.

Federal Scientific Center of the East Asia Terrestrial Biodiversity, Far Eastern Branch, Russian Academy of Sciences, 690022 Vladivostok, Russia.

出版信息

Antioxidants (Basel). 2022 Apr 3;11(4):709. doi: 10.3390/antiox11040709.

Abstract

Pterocarpans and related polyphenolics are known as promising neuroprotective agents. We used models of rotenone-, paraquat-, and 6-hydroxydopamine-induced neurotoxicity to study the neuroprotective activity of polyphenolic compounds from and their effects on mitochondrial membrane potential. We isolated 11 polyphenolic compounds: a novel coumestan lespebicoumestan A () and a novel stilbenoid 5'-isoprenylbicoloketon () as well as three previously known pterocarpans, two pterocarpens, one coumestan, one stilbenoid, and a dimeric flavonoid. Pterocarpans and , stilbenoid , and dimeric flavonoid significantly increased the percentage of living cells after treatment with paraquat (PQ), but only pterocarpan slightly decreased the ROS level in PQ-treated cells. Pterocarpan and stilbenoid were shown to effectively increase mitochondrial membrane potential in PQ-treated cells. We showed that pterocarpans and , containing a 3'-methyl-3'-isohexenylpyran ring; pterocarpens and , with a double bond between C-6a and C-11a; and coumestan significantly increased the percentage of living cells by decreasing ROS levels in 6-OHDA-treated cells, which is in accordance with their rather high activity in DPPH and FRAP tests. Compounds and effectively increased the percentage of living cells after treatment with rotenone but did not significantly decrease ROS levels.

摘要

紫檀烷类及相关多酚类化合物被认为是很有前景的神经保护剂。我们使用鱼藤酮、百草枯和6 - 羟基多巴胺诱导的神经毒性模型,研究了[植物名称未给出]中多酚类化合物的神经保护活性及其对线粒体膜电位的影响。我们分离出了11种多酚类化合物:一种新型香豆雌酚类化合物莱斯贝比香豆雌酚A([具体结构未给出])和一种新型芪类化合物5'-异戊烯基双洛酮([具体结构未给出]),以及三种先前已知的紫檀烷类化合物、两种紫檀素类化合物、一种香豆雌酚类化合物、一种芪类化合物和一种二聚黄酮类化合物。紫檀烷类化合物[具体化合物名称未给出]和[具体化合物名称未给出]、芪类化合物[具体化合物名称未给出]和二聚黄酮类化合物[具体化合物名称未给出]在百草枯(PQ)处理后显著提高了活细胞的百分比,但只有紫檀烷类化合物[具体化合物名称未给出]略微降低了PQ处理细胞中的活性氧水平。紫檀烷类化合物[具体化合物名称未给出]和芪类化合物[具体化合物名称未给出]被证明能有效提高PQ处理细胞中的线粒体膜电位。我们发现,含有3'-甲基-3'-异己烯基吡喃环的紫檀烷类化合物[具体化合物名称未给出]和[具体化合物名称未给出];在C-6a和C-11a之间有双键的紫檀素类化合物[具体化合物名称未给出]和[具体化合物名称未给出];以及香豆雌酚类化合物[具体化合物名称未给出],通过降低6 - 羟基多巴胺处理细胞中的活性氧水平,显著提高了活细胞的百分比,这与它们在DPPH和FRAP测试中相当高的活性一致。化合物[具体化合物名称未给出]和[具体化合物名称未给出]在鱼藤酮处理后有效提高了活细胞的百分比,但没有显著降低活性氧水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/496c/9025851/b2ac39f232a4/antioxidants-11-00709-g001a.jpg

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