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接骨木根的镇惊、镇痛和抗炎作用 被引量:5
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作者 吴春福 刘雯 +1 位作者 于庆海 郭月英 《中药材》 CAS CSCD 北大核心 1992年第1期35-37,共3页
小鼠皮下注射或腹腔注射接骨木水提物0.34、0.68、1.35g/kg可对抗土的宁或咖啡因诱发的惊厥反应。对小鼠醋酸扭体反应和醋酸诱发的毛细血管通透性增高均有明显抑制作用。大鼠腹腔注射接骨木水提物1.35g/kg或2.70g/kg可明显抑制由右旋糖... 小鼠皮下注射或腹腔注射接骨木水提物0.34、0.68、1.35g/kg可对抗土的宁或咖啡因诱发的惊厥反应。对小鼠醋酸扭体反应和醋酸诱发的毛细血管通透性增高均有明显抑制作用。大鼠腹腔注射接骨木水提物1.35g/kg或2.70g/kg可明显抑制由右旋糖酐或角叉菜胶引起的足跖肿胀。 展开更多
关键词 接骨木 根药理学
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紫茉莉根对前列腺增生大鼠前列腺组织CD34、Ki67抗原表达的影响 被引量:1
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作者 王峻 陈铭 +1 位作者 谢建兴 崔学教 《广州中医药大学学报》 CAS 2011年第2期167-170,215,216,共6页
【目的】观察紫茉莉根对前列腺增生(BPH)大鼠前列腺组织Ki67、CD34抗原表达的影响。【方法】选用SD大鼠,随机分为正常对照组,增生模型组,阴性对照组(灌胃生理盐水),紫茉莉根低、高剂量组(剂量分别为30、150 g.kg-1.d-1),非那雄胺组(剂量... 【目的】观察紫茉莉根对前列腺增生(BPH)大鼠前列腺组织Ki67、CD34抗原表达的影响。【方法】选用SD大鼠,随机分为正常对照组,增生模型组,阴性对照组(灌胃生理盐水),紫茉莉根低、高剂量组(剂量分别为30、150 g.kg-1.d-1),非那雄胺组(剂量为1 mg.kg-1.d-1),除正常对照组外,其他组大鼠均皮下注射丙酸睾丸素(剂量为5 mg/kg,连续21 d)复制BPH模型;造模结束后,各组分别按设计剂量给药,连续30 d。第51天处死大鼠取各组大鼠前列腺进行组织病理检查,采用免疫组化法检测各组大鼠前列腺组织Ki67、CD34抗原表达。【结果】病理检查结果显示:增生模型组和阴性对照组前列腺组织细胞增生活跃,紫茉莉根高、低剂量组与非那雄胺组均可一定程度改善前列腺细胞增生的病理变化。增生模型组与阴性对照组Ki67与CD34表达水平升高,与正常对照组比较差异有显著性意义(P<0.01);紫茉莉根高、低剂量组与非那雄胺组均可降低Ki67、CD34表达水平,与增生模型组和阴性对照组比较差异有显著性意义(P<0.01),而3个给药组间比较差异无显著性意义(P>0.05)。【结论】紫茉莉根抗BPH的作用与降低前列腺组织Ki67、CD34抗原表达水平,抑制前列腺细胞增殖和新生血管产生有关。 展开更多
关键词 紫茉莉/药理学 前列腺增生/中药疗法 前列腺/病理学 疾病模型 动物 大鼠
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Chondrogenic differentiation of rat bone marrow mesenchymal stem cells induced by puerarin and tetrandrine 被引量:1
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作者 Xin-Ran Dong Meng-Jiao Hu +2 位作者 Hui-Xin Pan Ke-Feng Li Yuan-Lu Cui 《Acupuncture and Herbal Medicine》 2022年第2期130-138,共9页
Objective: This study aims to clarify the effect of the active components puerarin and tetrandrine on the chondrogenic differentiation of bone marrow mesenchymal stem cells(BMSCs).Methods: Using network pharmacology, ... Objective: This study aims to clarify the effect of the active components puerarin and tetrandrine on the chondrogenic differentiation of bone marrow mesenchymal stem cells(BMSCs).Methods: Using network pharmacology, protein targets of puerarin and tetrandrine were predicted, and a database of cartilage formation targets was established. The protein target information related to disease was then collected, and the drug-targeting network was constructed by analyzing the protein–protein interactions. Genes related to chondrogenesis induced by puerarin and tetrandrine and chondroblast differentiation signaling pathways were searched. Finally, potential drug-and disease-related genes,as well as proteins, were screened and verified using real-time RT-PCR and western blotting.Results: Network pharmacological studies have shown that puerarin and tetrandrine are involved in BMSCs cartilage differentiation. The experimental results showed that puerarin and tetrandrine could regulate the expression of cartilage differentiation-related genes and proteins. Puerarin increased the protein expression of COL2 A1, COL10 A1, MMP13, and SOX-9,as well as the gene expression of Col2 a1, Mmp13, Tgfb1, and Sox-9. Tetrandrine increased the protein expression of COL2 A1,COL10 A1, MMP13, and SOX-9, as well as the gene expression of Col10 a1, Tgfb1, Sox-9, and Acan. The combination of puerarin and tetrandrine increased the protein expression of COL2 A1, COL10 A1, MMP13, and SOX-9 and the gene expression of Col2 a1,Col10 a1, Sox-9, and Acan.Conclusions: Puerarin, tetrandrine, and their combination can promote the proliferation of BMSCs and induce their differentiation into chondrocytes, and they are thus expected to be inducers of chondrogenic differentiation. These results suggest that puerarin and tetrandrine have potential therapeutic effects on osteoarthritis. 展开更多
关键词 Bone marrow mesenchymal stem cells(BMSCs) Chondrogenic differentiation Network pharmacology PUERARIN TETRANDRINE
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