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丹参素可防止 6-羟多巴胺诱导的 PC12 细胞体外损伤和斑马鱼多巴胺能神经元损伤。

Danshensu protects against 6-hydroxydopamine-induced damage of PC12 cells in vitro and dopaminergic neurons in zebrafish.

机构信息

State Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Sciences, Avenue Padre Tomás Pereira S.J., Macao.

出版信息

Neurosci Lett. 2013 May 24;543:121-5. doi: 10.1016/j.neulet.2013.02.069. Epub 2013 Apr 3.

Abstract

The overproduction of reactive oxygen species (ROS) has been implicated in the development of neurodegenerative diseases such as Parkinson's disease (PD) and Alzheimer's disease (AD). Previous studies have indicated that danshensu (beta-3,4-dihydroxyphenyl-lactic acid), a main hydrophilic component of the Chinese materia medica Radix Salviae Miltiorrhizae (Danshen, Pharmacopoeia of PR China), has ROS scavenging and antioxidant activities, however its mechanism of action was not clear. In this study, we investigated whether the protective effects of danshensu against neurotoxin 6-hydroxydopamine (6-OHDA)-induced oxidative stress involved the Nrf2/HO-1 pathways. Pretreatment with danshensu in PC12 cells significantly attenuated 6-OHDA-induced cytotoxicity and the production of ROS. Danshensu activated the nuclear translocation of Nrf2 to increase heme oxygenase-1 (HO-1), conferring protection against ROS. Danshensu induced the phosphorylation of Akt, and its cytoprotective effect was abolished by PI3K, Akt and HO-1 inhibitors. These results confirmed the crucial role of PI3K/Akt and HO-1 signaling pathways as the underlying mechanistic action of danshensu. Taken together, the results suggest that danshensu enhances HO-1 expression to suppress 6-OHDA-induced oxidative damage via PI3K/Akt/Nrf2 signaling pathways. Moreover, 6-OHDA-induced dopaminergic neuronal loss in zebrafish could be reduced by danshensu, further supporting the neuroprotective potential of danshensu.

摘要

活性氧(ROS)的过度产生与帕金森病(PD)和阿尔茨海默病(AD)等神经退行性疾病的发展有关。先前的研究表明,丹参素(β-3,4-二羟基苯乳酸),中国药材丹参(《中国药典》)的主要亲水性成分,具有清除 ROS 和抗氧化活性,但作用机制尚不清楚。在这项研究中,我们研究了丹参素对神经毒素 6-羟多巴胺(6-OHDA)诱导的氧化应激的保护作用是否涉及 Nrf2/HO-1 途径。丹参素预处理 PC12 细胞可显著减轻 6-OHDA 诱导的细胞毒性和 ROS 产生。丹参素激活 Nrf2 的核易位以增加血红素加氧酶-1(HO-1),从而提供对 ROS 的保护。丹参素诱导 Akt 的磷酸化,PI3K、Akt 和 HO-1 抑制剂可消除其细胞保护作用。这些结果证实了 PI3K/Akt 和 HO-1 信号通路作为丹参素潜在作用机制的关键作用。总之,结果表明丹参素通过 PI3K/Akt/Nrf2 信号通路增强 HO-1 的表达,抑制 6-OHDA 诱导的氧化损伤。此外,丹参素可减少 6-OHDA 诱导的斑马鱼多巴胺能神经元丢失,进一步支持了丹参素的神经保护潜力。

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