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咖啡二萜卡瓦醇促进甲基乙二醛处理的人神经母细胞瘤 SH-SY5Y 细胞中线粒体的保护。

Mitochondrial Protection Promoted by the Coffee Diterpene Kahweol in Methylglyoxal-Treated Human Neuroblastoma SH-SY5Y Cells.

机构信息

Grupo de Estudos em Neuroquímica e Neurobiologia de Moléculas Bioativas, Universidade Federal de Mato Grosso (UFMT), Av. Fernando Corrêa da Costa, 2367, Cuiaba, MT, CEP 78060-900, Brazil.

Programa de Pós-Graduação em Química (PPGQ), Universidade Federal de Mato Grosso (UFMT), Cuiaba, MT, Brazil.

出版信息

Neurotox Res. 2020 Jan;37(1):100-110. doi: 10.1007/s12640-019-00107-w. Epub 2019 Sep 7.

DOI:10.1007/s12640-019-00107-w
PMID:31494842
Abstract

The coffee diterpene kahweol (KW; CHO) is a cytoprotective agent exhibiting potent antioxidant actions, as demonstrated in several experimental models. In spite of the efforts to elucidate exactly how KW promotes cytoprotection, it was not previously examined whether KW would be able to protect mitochondria of human cells undergoing redox stress. In the present work, we have treated the human neuroblastoma SH-SY5Y cell line with KW at 0.1-10 μM for 12 h prior to a challenge with methylglyoxal (MG), a reactive dicarbonyl that impairs mitochondrial function. We have found that KW at 10 μM suppressed the loss of mitochondrial membrane potential (MMP) and the bioenergetics decline (including decreased activity of the mitochondrial complexes I and V and reduced production of adenosine triphosphate, ATP) in the MG-treated SH-SY5Y cells. KW also prevented the MG-elicited generation of reactive oxygen and nitrogen species (ROS and RNS, respectively) in the SH-SY5Y cells. In this regard, KW exerted an antioxidant effect on the membranes of mitochondria obtained from the MG-treated cells. The mitochondria-related effects induced by KW were blocked by inhibition of the phosphoinositide 3-kinase (PI3K)/Akt or of the p38 mitogen-activated protein kinase (MAPK) signaling pathways. Moreover, silencing of the transcription factor nuclear factor E2-related factor 2 (Nrf2) suppressed the mitochondrial protection promoted by KW in the MG-challenged cells. Therefore, KW protected mitochondria by a mechanism associated with the PI3K/Akt and p38 MAPK/Nrf2 signaling pathways.

摘要

咖啡二萜卡瓦胡椒醇(KW;CHO)是一种细胞保护剂,具有很强的抗氧化作用,在几个实验模型中得到了证明。尽管人们努力阐明 KW 如何促进细胞保护,但之前尚未研究 KW 是否能够保护人类细胞中线粒体免受氧化还原应激。在本工作中,我们用 0.1-10 μM 的 KW 处理人神经母细胞瘤 SH-SY5Y 细胞 12 小时,然后用甲基乙二醛(MG)处理,MG 是一种破坏线粒体功能的反应性二羰基化合物。我们发现,10 μM 的 KW 抑制了 MG 处理的 SH-SY5Y 细胞中线粒体膜电位(MMP)的丧失和生物能下降(包括线粒体复合物 I 和 V 的活性降低以及三磷酸腺苷(ATP)的产生减少)。KW 还防止了 MG 在 SH-SY5Y 细胞中产生的活性氧和氮物质(ROS 和 RNS)。在这方面,KW 对 MG 处理的细胞中的线粒体膜发挥了抗氧化作用。KW 诱导的与线粒体有关的作用被磷酸肌醇 3-激酶(PI3K)/Akt 或 p38 丝裂原活化蛋白激酶(MAPK)信号通路的抑制所阻断。此外,转录因子核因子 E2 相关因子 2(Nrf2)的沉默抑制了 KW 在 MG 挑战的细胞中促进的线粒体保护。因此,KW 通过与 PI3K/Akt 和 p38 MAPK/Nrf2 信号通路相关的机制来保护线粒体。

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