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枸杞酰胺 A,一种酚酰胺二聚体,可防止 NMDA 诱导的神经毒性及体外潜在机制。

Lyciumamide A, a dimer of phenolic amide, protects against NMDA-induced neurotoxicity and potential mechanisms in vitro.

机构信息

Department of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, 710032, China.

Department of Pharmacy, Xi'an Children's Hospital, Xi'an, China.

出版信息

J Mol Histol. 2021 Jun;52(3):449-459. doi: 10.1007/s10735-020-09952-y. Epub 2021 Mar 23.

Abstract

Currently, the excessive activation of N-methyl-D-aspartate receptors (NMDARs) is considered to be a crucial mechanism of brain injury. Lycium barbarum A (LyA) is a dimer of phenol amides isolated from the fruit of Lycium barbarum. Our previous studies have shown that LyA has potential antioxidant activity. This study aimed to explore the neuroprotective effect of LyA and its potential mechanism. Firstly, the molecular docking was used to preliminarily explore the potential function of LyA to block NMDAR. Then, the ability of LyA was further verified by NMDA-induced human neuroblastoma SH-SY5Y cells in vivo. Treatment with LyA significantly attenuated NMDA-induced neuronal insults by increasing cell viability, reducing lactate dehydrogenase (LDH) release, and increasing cell survival. Meanwhile, LyA significantly reversed the increase in intracellular calcium and in ROS production induced by NMDA. Finally, the western blot indicated that LyA could suppress the Ca influx and increase the p-NR2B, p-CaMKII, p-JNK, and p-p38 level induced by NMDA. These above findings provide evidence that LyA protect against brain injury, and restraining NMDARs and suppressing mitochondrial oxidative stress and inhibiting cell apoptosis may be involved in the protective mechanism.

摘要

目前,N-甲基-D-天冬氨酸受体(NMDARs)的过度激活被认为是脑损伤的关键机制。枸杞酰胺 A(LyA)是从枸杞果实中分离出的酚酰胺二聚体。我们之前的研究表明,LyA 具有潜在的抗氧化活性。本研究旨在探讨 LyA 的神经保护作用及其潜在机制。首先,采用分子对接初步探讨 LyA 阻断 NMDAR 的潜在功能。然后,通过 NMDA 诱导的人神经母细胞瘤 SH-SY5Y 细胞在体内进一步验证 LyA 的能力。LyA 处理可通过增加细胞活力、降低乳酸脱氢酶(LDH)释放和增加细胞存活来显著减轻 NMDA 诱导的神经元损伤。同时,LyA 显著逆转了 NMDA 诱导的细胞内钙和 ROS 产生的增加。最后,Western blot 表明 LyA 可抑制 NMDA 诱导的 Ca 内流和 p-NR2B、p-CaMKII、p-JNK 和 p-p38 水平的增加。这些发现为 LyA 对抗脑损伤提供了证据,抑制 NMDARs 和抑制线粒体氧化应激以及抑制细胞凋亡可能参与了保护机制。

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