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Modulation of Fas-FasL related apoptosis by PBN in the early phases of choline deficient diet-mediated hepatocarcinogenesis in rats.

机译:PBN在大鼠胆碱缺乏饮食介导的肝癌发生早期对Fas-FasL相关凋亡的调节。

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摘要

This study focused on the detection of apoptosis related events in very early phases of choline-deficient (CD)-induced hepatocarcinogenesis (at 2-5 weeks). Flow cytometry of isolated intact primary hepatocytes from CD diet fed rats indicated increased expression of the apoptosis-associated protein Fas. Increased apoptosis in CD-treated livers was confirmed by Western blot analyses of caspases and cytochrome c. This study was also able to detect differences in apoptotic events following phenyl butyl nitrone (PBN) treatment. Fas expression was inhibited by PBN, indicating that PBN is anti-apoptotic. It is speculated that in the early stages of CD-induced hepatotoxicity, PBN is involved in inhibiting pro-inflammatory factor-driven apoptosis of normal hepatocytes, which protects against the initiation of carcinogenesis. The CD diet model is also considered as a model for non-alcoholic steatohepatitis (NASH) in humans and early expression of Fas could also be a good index of the progression of NASH.
机译:这项研究的重点是在胆碱缺陷(CD)诱导的肝癌发生的非常早期阶段(2-5周)检测凋亡相关事件。 CD饮食喂养的大鼠分离的完整原代肝细胞的流式细胞术表明凋亡相关蛋白Fas的表达增加。半胱天冬酶和细胞色素c的蛋白质印迹分析证实了CD治疗的肝脏中凋亡的增加。这项研究还能够检测出苯基丁基硝酮(PBN)处理后凋亡事件的差异。 Fas表达被PBN抑制,表明PBN具有抗凋亡作用。据推测,在CD诱导的肝毒性的早期,PBN参与抑制促炎因子驱动的正常肝细胞凋亡,从而防止癌变的开始。 CD饮食模型也被认为是人类非酒精性脂肪性肝炎(NASH)的模型,Fas的早期表达也可能是NASH进展的良好指标。

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