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栀子酰胺A通过ERK1/2和PI3K/AKT信号通路减轻血清剥夺损伤诱导的细胞凋亡。

Gardenamide A attenuated cell apoptosis induced by serum deprivation insult via the ERK1/2 and PI3K/AKT signaling pathways.

作者信息

Wang R, Yang J, Peng L, Zhao J, Mu N, Huang J, Lazarovici P, Chen H, Zheng W

机构信息

State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-Sen University, Guangzhou 510060, PR China.

Institute of Traditional Chinese Medicine and Natural Products, College of Pharmacy, Jinan University, Guangzhou 510632, PR China.

出版信息

Neuroscience. 2015 Feb 12;286:242-50. doi: 10.1016/j.neuroscience.2014.11.056. Epub 2014 Dec 6.

Abstract

Gardenamide A (GA) is a stable genipin derivative with neuroprotective properties. It rescued pheochromocytoma cell (PC12) sympathetic cultures and retinal neuronal cells from apoptosis insult induced by serum deprivation. GA attenuated the accumulation of intracellular reactive oxygen species (ROS) and the loss of mitochondrial membrane potential. Western blotting with specific phospho-antibodies indicated that GA increased the phosphorylation of both the protein kinase B (Akt) and the extracellular signal-regulated kinase (ERK1/2) in PC12 cells. The GA neuroprotective effect was inhibited by either the specific phosphoinositide 3-kinase (PI3K) inhibitor LY294002 or the mitogen-activated protein kinase (MAPK) pathway inhibitor PD98059. These results propose that the neuroprotective effect of GA on PC12 neuronal cell cultures was mediated through both the PI3K/Akt and ERK1/2 signaling pathways. Therefore, GA may serve as a pharmacological tool to investigate neuroprotective mechanisms of neurons afflicted by different insults.

摘要

栀子酰胺A(GA)是一种具有神经保护特性的稳定京尼平衍生物。它挽救了嗜铬细胞瘤细胞(PC12)交感神经培养物和视网膜神经元细胞,使其免受血清剥夺诱导的凋亡损伤。GA减轻了细胞内活性氧(ROS)的积累和线粒体膜电位的丧失。用特异性磷酸化抗体进行的蛋白质免疫印迹表明,GA增加了PC12细胞中蛋白激酶B(Akt)和细胞外信号调节激酶(ERK1/2)的磷酸化。GA的神经保护作用被特异性磷脂酰肌醇3激酶(PI3K)抑制剂LY294002或丝裂原活化蛋白激酶(MAPK)途径抑制剂PD98059所抑制。这些结果表明,GA对PC12神经元细胞培养物的神经保护作用是通过PI3K/Akt和ERK1/2信号通路介导的。因此,GA可作为一种药理学工具,用于研究受不同损伤的神经元的神经保护机制。

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