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左归丸通过调节骨桥蛋白/胰岛素样生长因子-1受体/磷酸酶和张力蛋白同源物及下游雷帕霉素靶蛋白信号通路促进神经突生长。

Zuogui Pill Promotes Neurite Outgrowth by Regulating OPN/ IGF-1R/PTEN and Downstream mTOR Signaling Pathway.

作者信息

Liu Yan, Wu Dan, Yan Xiaohui, Xu Xinyu, Zhu Jian, Li Changyin, Feng Qinghua, Li Li, Wu Minghua, Li Wenlei

机构信息

Department of Neurology, Jiangsu Province Hospital of Chinese Medicine, Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, 210029, China.

The First Clinical Medical College, Nanjing University of Chinese Medicine, Nanjing, 210029, China.

出版信息

Comb Chem High Throughput Screen. 2025;28(4):675-690. doi: 10.2174/0113862073295309240214060857.

Abstract

AIMS AND OBJECTIVES

Zuogui pill (ZGP) is the traditional Chinese medicine for tonifying kidney yin. Clinical and animal studies have shown that ZGP effectively enhances neurologic impairment after ischemic stroke, which may be related to promoting neurite outgrowth. This investigation aimed to prove the pro-neurite outgrowth impact of ZGP and define the underlying molecular pathway .

MATERIALS AND METHODS

The major biochemical components in the ZGP were investigated using UPLC-QTOF-MS. All-trans retinoic acid (ATRA) was employed to stimulate SH-SY5Y cells to develop into mature neurons, followed by oxygen-glucose deprivation and reoxygenation damage (OGD/R). Then the cells were supplemented with different concentrations of ZGP, and cell viability was identified by CCK-8. The neurites' outgrowth abilities were detected by wound healing test, while immunofluorescence staining of β-III-tubulin was used to label neurites and measure their length. Western blot was employed to discover the changes in protein levels.

RESULTS

ZGP improved the cell viability of differentiated SH-SY5Y cells following OGD/R damage, according to the CCK-8 assay. Concurrently, ZGP promoted neurite outgrowth and improved neurite crossing and migration ability. Protein expression analysis showed that ZGP upregulated the expression of GAP43, OPN, p-IGF-1R, mTOR, and p-S6 proteins but downregulated the expression of PTEN protein. Blocking assay with IGF-1R specific inhibitor Linstinib suggested IGF-1R mediated mTOR signaling pathway was involved in the pro-neurite outgrowth effect of ZGP.

CONCLUSION

This work illustrated the molecular mechanism underpinning ZGP's action and offered more proof of its ability to promote neurite outgrowth and regeneration following ischemic stroke.

摘要

目的与目标

左归丸是一种补肾阴的传统中药。临床和动物研究表明,左归丸能有效改善缺血性中风后的神经功能缺损,这可能与促进神经突生长有关。本研究旨在证实左归丸对神经突生长的促进作用,并确定其潜在的分子途径。

材料与方法

采用超高效液相色谱-四极杆飞行时间质谱联用技术(UPLC-QTOF-MS)研究左归丸中的主要生化成分。用全反式维甲酸(ATRA)刺激人神经母细胞瘤细胞(SH-SY5Y)分化为成熟神经元,然后进行氧糖剥夺/复氧损伤(OGD/R)。随后,用不同浓度的左归丸处理细胞,通过CCK-8法检测细胞活力。采用划痕实验检测神经突的生长能力,用β-III微管蛋白免疫荧光染色标记神经突并测量其长度。采用蛋白质免疫印迹法检测蛋白水平的变化。

结果

CCK-8检测结果显示,左归丸可提高OGD/R损伤后分化的SH-SY5Y细胞的活力。同时,左归丸促进神经突生长,提高神经突的交叉和迁移能力。蛋白表达分析表明,左归丸上调生长相关蛋白43(GAP43)、骨桥蛋白(OPN)、磷酸化胰岛素样生长因子1受体(p-IGF-1R)、哺乳动物雷帕霉素靶蛋白(mTOR)和磷酸化核糖体蛋白S6(p-S6)的表达,但下调磷酸酶和张力蛋白同源物(PTEN)的表达。用胰岛素样生长因子1受体特异性抑制剂林司替尼进行阻断实验表明,胰岛素样生长因子1受体介导的mTOR信号通路参与了左归丸促进神经突生长的作用。

结论

本研究阐明了左归丸作用的分子机制,为其促进缺血性中风后神经突生长和再生的能力提供了更多证据。

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