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Spasmolytic Mechanism of Aqueous Licorice Extract on Oxytocin-Induced Uterine Contraction through Inhibiting the Phosphorylation of Heat Shock Protein 27

机译:甘草水提取物通过抑制热休克蛋白27的磷酸化对催产素引起的子宫收缩的痉挛机制。

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Licorice derived from the roots and rhizomes of Glycyrrhiza uralensis Fisch. (Fabaceae), is one of the most widely-used traditional herbal medicines in China. It has been reported to possess significant analgesic activity for treating spastic pain. The aim of this study is to investigate the spasmolytic molecular mechanism of licorice on oxytocin-induced uterine contractions and predict the relevant bioactive constituents in the aqueous extract. The aqueous extraction from licorice inhibited the amplitude and frequency of uterine contraction in a concentration-dependent manner. A morphological examination showed that myometrial smooth muscle cells of oxytocin-stimulated group were oval-shaped and arranged irregularly, while those with a single centrally located nucleus of control and licorice-treated groups were fusiform and arranged orderly. The percentage of phosphorylation of HSP27 at Ser-15 residue increased up to 50.33% at 60 min after oxytocin stimulation. Furthermore, this increase was significantly suppressed by licorice treatment at the concentration of 0.2 and 0.4 mg/mL. Colocalization between HSP27 and α-SMA was observed in the myometrial tissues, especially along the actin bundles in the oxytocin-stimulated group. On the contrary, the colocalization was no longer shown after treatment with licorice. Additionally, employing ChemGPS-NP provided support for a preliminary assignment of liquiritigenin and isoliquiritigenin as protein kinase C (PKC) inhibitors in addition to liquiritigenin, isoliquiritigenin, liquiritin and isoliquiritin as MAPK-activated protein kinase 2 (MK2) inhibitors. These assigned compounds were docked with corresponding crystal structures of respective proteins with negative and low binding energy, which indicated a high affinity and tight binding capacity for the active site of the kinases. These results suggest that licorice exerts its spasmolytic effect through inhibiting the phosphorylation of HSP27 to alter the interaction between HSP27 and actin. Furthermore, our results provide support for the prediction that potential bioactive constituents from aqueous licorice extract inhibit the relevant up-stream kinases that phosphorylate HSP27. View Full-Text
机译:欧亚甘草来源于甘草根的根和根。 (豆科),是中国使用最广泛的传统草药之一。据报道具有治疗痉挛性疼痛的显着镇痛活性。这项研究的目的是研究甘草对催产素引起的子宫收缩的解痉分子机制,并预测水提取物中的相关生物活性成分。从甘草中提取水以浓度依赖的方式抑制子宫收缩的幅度和频率。形态学检查显示,催产素刺激组的肌层平滑肌细胞呈椭圆形且排列不规则,而对照组和甘草处理组的中央核位于单个核的细胞为梭形且排列有序。催产素刺激后60分钟,Her27在Ser-15残基的磷酸化百分比增加至50.33%。此外,在0.2和0.4mg / mL的浓度下通过甘草处理显着抑制了这种增加。在子宫肌层组织中观察到了HSP27与α-SMA之间的共定位,尤其是在催产素刺激组中的肌动蛋白束附近。相反,在用甘草治疗后不再显示共定位。此外,除Liquiritigenin,isoliquiritigenin,liquiritin和isoliquiritin作为MAPK激活的蛋白激酶2(MK2)抑制剂外,使用ChemGPS-NP还为liquiritigenin和isoliquiritigenin作为蛋白激酶C(PKC)抑制剂的初步分配提供了支持。这些分配的化合物与具有负结合能和低结合能的相应蛋白质的相应晶体结构对接,这表明对激酶活性位点具有高亲和力和紧密结合能力。这些结果表明,甘草通过抑制HSP27的磷酸化来改变HSP27与肌动蛋白之间的相互作用,发挥其痉挛作用。此外,我们的结果为以下预测提供了支持:甘草水溶液提取物的潜在生物活性成分会抑制磷酸化HSP27的相关上游激酶。查看全文

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