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木犀草素通过抑制 Akt/mTOR 信号通路防止镉诱导的 PC12 细胞死亡。

Luteolin prevents cadmium-induced PC12 cell death by suppressing the Akt/mTOR signaling pathway.

机构信息

School of Public Health, Bengbu Medical College, Bengbu, Anhui, China.

Anhui Provincial Center for Disease Control and Prevention, Hefei, Anhui, China.

出版信息

Medicine (Baltimore). 2024 Nov 1;103(44):e40372. doi: 10.1097/MD.0000000000040372.

Abstract

Cadmium (Cd) is an environmental pollutant that can cause neurodegenerative disorders. Luteolin (Lut) is a natural flavonoid compound. However, whether Lut protects against Cd-induced nerve cell death remains unclear. In the present study, PC12 cells were used to investigate the neuroprotective effect of Lut against Cd poisoning. Changes in cell viability, apoptosis, B-cell lymphoma-2 (Bcl-2) and Bcl-2-associated X protein expression, and protein kinase B (Akt)/mammalian target of rapamycin (mTOR) pathway activity were analyzed by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay, Hoechst 33258 staining, flow cytometry, and western blotting. Lut markedly attenuated the Cd-induced reduction in cell viability, nuclear fragmentation, condensation, and the decrease in the Bcl-2/Bcl-2-associated X protein ratio in PC12 cells. Furthermore, Lut blocked the Cd-mediated activation of the Akt/mTOR signaling pathway. Moreover, inhibition of the Akt/mTOR signaling pathway with LY294002 (a PI3K inhibitor) enhanced the protective effect of Lut against Cd-induced cell death by suppressing Cd-induced activation of Akt, mTOR, and eukaryotic initiation factor 4E binding protein 1. The results showed that Lut prevented Cd-induced cell death partly by blocking the Akt/mTOR signaling pathway. Lut may be a potential agent for preventing Cd-induced nerve cell damage and neurodegenerative diseases.

摘要

镉 (Cd) 是一种环境污染物,可导致神经退行性疾病。木犀草素 (Lut) 是一种天然黄酮类化合物。然而,Lut 是否能预防 Cd 诱导的神经细胞死亡尚不清楚。本研究采用 PC12 细胞探讨了 Lut 对 Cd 中毒的神经保护作用。通过 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐法、Hoechst 33258 染色、流式细胞术和 Western blot 分析细胞活力、细胞凋亡、B 细胞淋巴瘤-2 (Bcl-2) 和 Bcl-2 相关 X 蛋白表达以及蛋白激酶 B (Akt)/哺乳动物雷帕霉素靶蛋白 (mTOR) 信号通路活性的变化。Lut 显著减轻了 Cd 诱导的 PC12 细胞活力降低、核碎裂、浓缩以及 Bcl-2/Bcl-2 相关 X 蛋白比值降低。此外,Lut 阻断了 Cd 介导的 Akt/mTOR 信号通路的激活。此外,用 LY294002(一种 PI3K 抑制剂)抑制 Akt/mTOR 信号通路,通过抑制 Cd 诱导的 Akt、mTOR 和真核起始因子 4E 结合蛋白 1 的激活,增强了 Lut 对 Cd 诱导的细胞死亡的保护作用。结果表明,Lut 通过阻断 Akt/mTOR 信号通路部分预防了 Cd 诱导的细胞死亡。Lut 可能是预防 Cd 诱导的神经细胞损伤和神经退行性疾病的潜在药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66eb/11537648/02cc634ca86b/medi-103-e40372-g001.jpg

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