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栀子苷通过调节胰岛素降解酶的表达抑制 Aβ₁₋₄₂ 对皮质神经元的细胞毒性。

Geniposide regulates insulin-degrading enzyme expression to inhibit the cytotoxicity of Aβ₁₋₄₂ in cortical neurons.

机构信息

Research Centre of Medicinal Chemistry and Chemical Biology, Chongqing Technology and Business University, Chongqing 400067, PR China.

出版信息

CNS Neurol Disord Drug Targets. 2012 Dec;11(8):1045-51. doi: 10.2174/1871527311211080015.

Abstract

We reported previously that geniposide showed neurotrophic and neuroprotective activities with the activation of glucagons-like peptide 1 receptor (GLP-1R) in neurons. The current study was designed to further investigate the protective effect of geniposide on β-amyloid (Aβ)-induced cytotoxicity. Our results showed that pre-incubation with geniposide prevented Aβ₁₋₄₂-induced cell injury in primary cultured cortical neurons. Geniposide also induced the expression of insulin-degrading enzyme (IDE), a major degrading protease of Aβ, in a dose-dependent manner. Moreover, bacitracin, an inhibitor of IDE, and RNAi on Glp-1r gene decreased the neuroprotection of geniposide in Aβ₁₋₄₂-treated cortical neurons. Our findings indicated that geniposide activating GLP-1R to against Aβ-induced neurotoxicity involved in its regulation on the expression of IDE in cortical neurons, which provided an additional mechanistic insight into the role of GLP-1R in neuroprotection.

摘要

我们之前曾报道过,栀子苷通过激活神经元中的胰高血糖素样肽 1 受体(GLP-1R)表现出神经营养和神经保护活性。本研究旨在进一步探讨栀子苷对β-淀粉样蛋白(Aβ)诱导的细胞毒性的保护作用。我们的结果表明,栀子苷预处理可预防原代培养皮质神经元中 Aβ₁₋₄₂诱导的细胞损伤。栀子苷还以剂量依赖性方式诱导胰岛素降解酶(IDE)的表达,IDE 是 Aβ 的主要降解蛋白酶。此外,IDE 的抑制剂 bacitracin 和 Glp-1r 基因的 RNAi 降低了栀子苷在 Aβ₁₋₄₂处理的皮质神经元中的神经保护作用。我们的研究结果表明,栀子苷通过激活 GLP-1R 来对抗 Aβ 诱导的神经毒性,涉及它对皮质神经元中 IDE 表达的调节,这为 GLP-1R 在神经保护中的作用提供了更多的机制见解。

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