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

被引:20
作者
Inoue, Yoshiko
Asanuma, Taketoshi
Smith, Nataliya
Saunders, Debra
Oblander, Jenny
Kotake, Yashige
Floyd, Robert A.
Towner, Rheal A.
机构
[1] Oklahoma Med Res Fdn, Free Radical Biol & Aging Res Program, Oklahoma City, OK 73104 USA
[2] Oklahoma Med Res Fdn, Small Anim MRI Core Facil, Oklahoma City, OK 73104 USA
[3] Oklahoma Med Res Fdn, Lab Anim Resource Ctr, Oklahoma City, OK 73104 USA
[4] Hokkaido Univ, Grad Sch Vet Med, Dept Environm Vet Sci, Sapporo, Hokkaido, Japan
关键词
choline-deficient diet; hepatocarcinogenesis; apoptosis; phenyl butyl nitrone (PBN); rats;
D O I
10.1080/10715760701447322
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
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 antiapoptotic. It is speculated that in the early stages of CD-induced hepatotoxicity, PBN is involved in inhibiting proinflammatory 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.
引用
收藏
页码:972 / 980
页数:9
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