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机构地区:[1]贵阳医学院病理学教研室,贵州贵阳550004 [2]贵阳医学院附院病理科,贵州贵阳550004 [3]贵阳医学院附院感染科,贵州贵阳550004
出 处:《贵阳医学院学报》2013年第6期588-592,597,共6页Journal of Guiyang Medical College
基 金:国家重点研究计划(973)课题(NO.2011CB512114);贵州省科技计划课题(黔科合SZ[2011]3001)
摘 要:目的:研究不同白酒对酒精性肝纤维化、肝硬化合并肝癌大鼠肝组织中Kruppule样因子6(Klf 6)及相关基因表达的影响。方法:运用2种白酒和黄曲霉素B1(AFB1)对大鼠进行处理,制备酒精性肝纤维化、肝硬化合并肝癌大鼠模型。用免疫组织化学法检测模型大鼠肝脏组织Klf 6、转化生长因子-β1(TGF-β1)、p21及α-平滑肌动蛋白(α-SMA)的表达水平。RT-PCR技术检测大鼠肝脏组织中Klf 6基因mRNA表达水平。结果:成功制备了酒精性肝纤维化、肝硬化合并肝癌大鼠模型,不同白酒诱导大鼠肝纤维化、肝硬化合并肝癌的程度不同。Klf 6、p21在白酒A组(AD组和AG组)的表达率高于白酒B组(BD组和BG组),差异有统计学意义(P<0.05);TGF-β1,α-SMA在白酒B组(BD组和BG组)表达高于白酒B组(BD组和BG组),差异有统计学意义(P<0.05)。RT-PCR结果显示,白酒A组(AD组和AG组)肝组织Klf 6基因的mRNA表达高于白酒B组(BD组和BG组),差异有统计学意义(P<0.05)。结论:不同白酒对酒精性肝纤维化,肝硬化合并肝癌大鼠肝脏Klf 6、p21、TGF-β1和α-SMA的表达不同,可能是导致酒精性肝病(ALD)的程度不同的机制之一。Objective: To discuss the expression of Klf 6 and related gene in hepatic fibrosis, and hepatocirrhosis with hepatoma tissue rats administered with different liquor. Methods: The hepatic fi- brosis and hepatocirrhosis with hepatoma rat model was made with aflatoxin B1 ( AFB1 ) and 2 liquor (liquor A and B with low and high content) respectively, and the control rats were administered with distill water. The protein expressions of Kruppel-like factor 6 (Klf 6), transforming growth factor-J51 (TGF-[M), p21, and alpha smooth muscle actin (ot-SMA) in liver were detected with immunohisto- chemistry method, and the mRNA level were evaluated with RT-PCR after the rats were decapitated. Results: The hepatic fibrosis and hepatocirrhosis with hepatoma rat model was made successfully, and rat models induced by different liquor showed pathological changes with different severity. The expres- sion of Klf 6 ( protein and mRNA level) AD) and high-content group (group AG BD) and high-content group (group BG and p21 (protein level) of liquor A low-content group (group were higher than those of liquor B low-content group ( group with statistical significance (P 〈 0.05 ). However, the pro-tein expression of TGF-I31 and oL-SMA increased in BD and BG groups contrasted with AD, AG and control groups ( P 〈 0.05 ). Conclusions: The degree of the effects of different liquor on the expression of Klf 6, TGF-B1, p21, and ot-SMA is different, which may contribute to the different inducing effects on hepatic fibrosis, hepatocirrhosis and hepatocirrhosis with hepatoma.
关 键 词:肝疾病 酒精性 纤维化 肝硬化 酒精性 肝肿瘤 Kruppule样因子6 蛋白质 P21 α-平滑肌动蛋 白
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