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首页> 外文期刊>Nutrition Research and Practice >Anti-fibrotic effects of Orostachys japonicus A. Berger (Crassulaceae) on hepatic stellate cells and thioacetamide-induced fibrosis in rats
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Anti-fibrotic effects of Orostachys japonicus A. Berger (Crassulaceae) on hepatic stellate cells and thioacetamide-induced fibrosis in rats

机译:日本牛膝对肝星状细胞和硫代乙酰胺诱导的纤维化的抗纤维化作用

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BACKGROUND/OBJECTIVE Orostachys japonicus A. Berger (Crassulaceae) has been used in traditional herbal medicines in Korea and other Asian countries to treat various diseases, including liver disorders. In the present study, the anti-fibrotic effects of O. japonicus extract (OJE) in cellular and experimental hepatofibrotic rat models were investigated. MATERIALS/METHODS An in vitro hepatic stellate cells (HSCs) system was used to estimate cell viability, cell cycle and apoptosis by MTT assay, flow cytometry, and Annexin V-FITC/PI staining techniques, respectively. In addition, thioacetamide (TAA)-induced liver fibrosis was established in Sprague Dawley rats. Briefly, animals were divided into five groups (n = 8): Control, TAA, OJE 10 (TAA with OJE 10 mg/kg), OJE 100 (TAA with OJE 100 mg/kg) and silymarin (TAA with Silymarin 50 mg/kg). Fibrosis was induced by treatment with TAA (200 mg/kg, i.p. ) twice per week for 13 weeks, while OJE and silymarin were administered orally two times per week from week 7 to 13. The fibrotic related gene expression serum biomarkers glutathione and hydroxyproline were estimated by RT-PCR and spectrophotometry, respectively, using commercial kits. RESULTS OJE (0.5 and 0.1 mg/mL) and silymarin (0.05 mg/mL) treatment significantly ( P CONCLUSIONS OJE can be developed as a potential agent for the treatment of hepatofibrosis.
机译:背景/目的Orostachys japonicus A. Berger(景天科)已在韩国和其他亚洲国家用于传统草药中,用于治疗各种疾病,包括肝脏疾病。在本研究中,研究了日本槐提取物(OJE)在肝纤维化和实验性肝纤维化大鼠模型中的抗纤维化作用。材料/方法使用体外肝星状细胞(HSC)系统分别通过MTT分析,流式细胞术和Annexin V-FITC / PI染色技术评估细胞活力,细胞周期和凋亡。此外,在Sprague Dawley大鼠中建立了硫代乙酰胺(TAA)诱导的肝纤维化。简而言之,将动物分为五组(n = 8):对照组,TAA,OJE 10(TAA含OJE 10 mg / kg),OJE 100(TAA含OJE 100 mg / kg)和水飞蓟素(TAA含水飞蓟素50 mg / kg)。公斤)。每周两次用TAA(200 mg / kg,ip)治疗诱导纤维化,持续13周,而从第7周到13周,每周两次口服OJE和水飞蓟素。纤维化相关基因表达的血清生物标志物谷胱甘肽和羟脯氨酸为使用市售试剂盒分别通过RT-PCR和分光光度法估算。结果OJE(0.5和0.1 mg / mL)和水飞蓟素(0.05 mg / mL)的治疗效果显着(P结论OJE可以开发为治疗肝纤维化的潜在药物。

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