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中药“人参养荣汤”的组成成分之一川芎嗪可逆转年龄相关性脱髓鞘。

Administration of chinpi, a component of the herbal medicine ninjin-youei-to, reverses age-induced demyelination.

机构信息

Department of Neuroglia Cell Biology, Tokyo Metropolitan Institute of Gerontology, 35-2 Sakae-cho, Itabashi-ku, Tokyo 173-0015, Japan.

出版信息

Evid Based Complement Alternat Med. 2011;2011:617438. doi: 10.1093/ecam/neq001. Epub 2011 Jun 5.

DOI:10.1093/ecam/neq001
PMID:21799684
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3138645/
Abstract

The disruption of myelin causes severe neurological diseases. An understanding of the mechanism of myelination and remyelination is essential for the development of therapeutic strategies for demyelination diseases. Our previous findings indicated that the FcRγ/Fyn cascade is a potential therapeutic target for remyelination caused by the Chinese/Japanese traditional herbal (Kampo) medicine ninjin'youeito (Ninjin-youei-to, NYT), which is a hot-water extract made from 12 medicinal herbs. To identify which constituents of NYT are involved in the reversal of demyelination and to examine the potential therapeutic effect, we tested several of the chemical constituents of NYT. Here, we report that Chinpi, a constituent of NYT, upregulates the FcRγ/Fyn signaling cascade resulting in a potentially therapeutic effect against age-induced demyelination. In addition, we observed that phosphorylated (activated) FcRγ/Fyn upregulated the expression of the 21.5 kDa isoform of myelin basic protein, inducing rapid morphological differentiation, when oligodendrocyte precursor cells (OPCs) were cultured in the presence of hesperidin and/or narirutin (the major active constituents of Chinpi). These results suggest that hesperidin and narirutin participate in the FcRγ/Fyn signaling pathway in OPCs causing these cells to differentiate into myelinating oligodendrocytes.

摘要

髓鞘的破坏会导致严重的神经疾病。了解髓鞘形成和再髓鞘化的机制对于开发脱髓鞘疾病的治疗策略至关重要。我们之前的研究结果表明,FcRγ/Fyn 级联反应是一种潜在的治疗靶点,可用于治疗中国/日本传统草药(汉方)药物人参保肺汤(Ninjin-youei-to,NYT)引起的髓鞘再生,NYT 是由 12 种草药制成的热水提取物。为了确定 NYT 中的哪些成分参与脱髓鞘的逆转,并研究潜在的治疗效果,我们测试了 NYT 的几种化学成分。在这里,我们报告 Chinpi,NYT 的一种成分,可上调 FcRγ/Fyn 信号级联反应,从而对年龄相关性脱髓鞘产生潜在的治疗作用。此外,我们观察到,当寡突细胞前体细胞(OPC)在橙皮苷和/或川陈皮素(Chinpi 的主要活性成分)存在的情况下培养时,磷酸化(激活)的 FcRγ/Fyn 上调了 21.5kDa 同工型髓鞘碱性蛋白的表达,从而诱导快速形态分化。这些结果表明,橙皮苷和川陈皮素参与了 OPC 中的 FcRγ/Fyn 信号通路,导致这些细胞分化为髓鞘形成的少突胶质细胞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6148/3138645/2b2632d6cae1/ECAM2011-617438.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6148/3138645/fc3d1610bf04/ECAM2011-617438.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6148/3138645/c55cee5d5dcc/ECAM2011-617438.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6148/3138645/88480091222c/ECAM2011-617438.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6148/3138645/fe9853d1f07a/ECAM2011-617438.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6148/3138645/c54e37b0e002/ECAM2011-617438.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6148/3138645/2b2632d6cae1/ECAM2011-617438.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6148/3138645/fc3d1610bf04/ECAM2011-617438.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6148/3138645/c55cee5d5dcc/ECAM2011-617438.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6148/3138645/88480091222c/ECAM2011-617438.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6148/3138645/fe9853d1f07a/ECAM2011-617438.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6148/3138645/c54e37b0e002/ECAM2011-617438.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6148/3138645/2b2632d6cae1/ECAM2011-617438.006.jpg

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