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黄芩中的黄酮类化合物作为潜在的中风治疗药物,通过靶向突触后密度蛋白95(PSD-95)的第二个突触后致密物95(PSD-95)/盘状大蛋白/紧密连接蛋白1(PDZ)结构域发挥作用。

Flavonoids from Radix Scutellariae as potential stroke therapeutic agents by targeting the second postsynaptic density 95 (PSD-95)/disc large/zonula occludens-1 (PDZ) domain of PSD-95.

作者信息

Tang W, Sun X, Fang J S, Zhang M, Sucher N J

机构信息

Department of Biology, Hong Kong University of Science & Technology, Clear Water Bay, Kowloon, Hong Kong SAR, China.

出版信息

Phytomedicine. 2004;11(4):277-84. doi: 10.1078/0944711041495173.

Abstract

Excessive activation of N-methyl-D-aspartate receptors (NMDARs) and subsequent production of nitric oxide by neuronal nitric oxide synthase (nNOS) contribute to neuronal damage resulting from hypoxic and ischemic insults. NMDARs and nNOS are coupled together at the postsynaptic membrane through their interaction with postsynaptic density protein (PSD) 95 via PSD-95/disc large/zonula occludens-1 (PDZ) domains. We used NMR (nuclear magnetic resonance) spectroscopy to screen medicinal herbs used in traditional Chinese medicine (TCM) stroke therapy for compounds binding to the second PDZ domain (PDZ2) of PSD-95, the domain linking nNOS and PSD-95. Aqueous extract of Huangqin, the root of Scutellaria baicalensis Georgi (Labiatae), showed significant binding to PDZ2 of PSD-95. The binding site of the active components in the extract overlapped with the nNOS/NR2B-binding pocket of PDZ2 of PSD-95. Four flavones, baicalin, norwogonoside, oroxylin A-glucuronide (oroxyloside), and wogonoside were isolated and found to account for the PDZ-binding activity of the extract. NMR titration experiments showed that baicalin and norwogonoside displayed the highest PDZ2 binding affinity, while oroxylin A-glucuronide and wogonoside showed 4-5 fold less potency in binding to the PDZ domain. Identification of the PDZ binding activity of these compounds will allow investigating whether or not it contributes to the observed clinical effects of Radix Scutellariae. Furthermore, these molecules might provide leads for the development of drugs targeting the signaling pathways mediated by PDZ domains.

摘要

N-甲基-D-天冬氨酸受体(NMDARs)的过度激活以及随后神经元型一氧化氮合酶(nNOS)产生一氧化氮,会导致缺氧和缺血性损伤引起的神经元损伤。NMDARs和nNOS通过与突触后致密蛋白(PSD)95经由PSD-95/盘状大蛋白/紧密连接蛋白-1(PDZ)结构域相互作用,在突触后膜上耦合在一起。我们使用核磁共振(NMR)光谱法,筛选用于中医中风治疗的草药中与PSD-95的第二个PDZ结构域(PDZ2)结合的化合物,该结构域连接nNOS和PSD-95。黄芩(唇形科植物黄芩的根)的水提取物显示出与PSD-95的PDZ2有显著结合。提取物中活性成分的结合位点与PSD-95的PDZ2的nNOS/NR2B结合口袋重叠。分离出四种黄酮,黄芩苷、去甲黄芩苷、木犀草素A-葡萄糖醛酸苷(木犀草苷)和汉黄芩苷,发现它们是提取物中PDZ结合活性的原因。NMR滴定实验表明,黄芩苷和去甲黄芩苷表现出最高的PDZ2结合亲和力,而木犀草素A-葡萄糖醛酸苷和汉黄芩苷与PDZ结构域的结合能力低4至5倍。鉴定这些化合物的PDZ结合活性将有助于研究其是否对黄芩的临床疗效有贡献。此外,这些分子可能为开发靶向由PDZ结构域介导的信号通路的药物提供线索。

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