首页> 外文期刊>The Journal of toxicological sciences >The anti-apoptotic effect of fucoxanthin on carbon tetrachloride-induced hepatotoxicity.
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The anti-apoptotic effect of fucoxanthin on carbon tetrachloride-induced hepatotoxicity.

机译:岩藻黄质对四氯化碳诱导的肝毒性的抗凋亡作用。

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This study evaluated the anti-apoptotic activity of fucoxanthin in carbon tetrachloride (CCl(4))-induced hepatotoxicity. An in vitro study using the 3-(4,5-dimethylthiazol-2-yl) 2,5-diphenyltetrazolium bromide (MTT) assay clearly demonstrated an attenuation of CCl(4)-induced hepatotoxicity with fucoxanthin. This effect was dose-dependent; 25 μM was more effective than 10 μM of fucoxanthin for attenuating the hepatotoxicity induced by 5 mM of CCl(4). Acute CCl(4)-hepatotoxicity in rats, with numerous cells positive for the terminal deoxynucleotidyl - transferase (TdT) -mediated deoxyuridine triphosphate-digoxigenin (dUTP) nick-end labeling (TUNEL) stain were seen in the pericentral area of the hepatic lobule. Oral pretreatment of CCl(4)- injected rats with fucoxanthin significantly reduced hepatocyte apoptosis. Fucoxanthin was immunohistochemically shown to increase heme oxygenase-1 expression in the cultured liver cells of Hc cells and TRL1215 cells. By oral pretreatment of CCl(4)-injected rats with fucoxanthin, the hepatic heme oxygenase-1 protein levels were significantly increased compared to those not pretreated with fucoxanthin. Heme oxygenase-1 mRNA expression after CCl(4 )injection was higher in the CCl(4)+fucoxanthin group than in the CCl(4 )group, although the difference was not significant. The findings suggest that fucoxanthin attenuates hepatocyte apoptosis through heme oxygenase-1 induction in CCl(4)-induced acute liver injury.
机译:这项研究评估了岩藻黄质在四氯化碳(CCl(4))诱导的肝毒性中的抗凋亡活性。体外研究使用3-(4,5-二甲基噻唑-2-基)2,5-二苯基四唑溴化物(MTT)测定法清楚地证明了岩藻黄质减弱了CCl(4)诱导的肝毒性。这种作用是剂量依赖性的。 25μM比岩藻黄质比10μM更有效地减轻了5 mM CCl(4)诱导的肝毒性。大鼠急性CCl(4)-肝毒性,在肝小叶的中央周围区域观察到大量的细胞为末端脱氧核苷酸-转移酶(TdT)介导的脱氧尿苷三磷酸-地高辛苷(dUTP)缺口末端标记(TUNEL)染色。岩藻黄质口服CCl(4)注射大鼠的预处理显着降低了肝细胞凋亡。免疫组化显示褐藻黄质增加了Hc细胞和TRL1215细胞培养的肝细胞中血红素加氧酶-1的表达。与未经岩藻黄质预处理的大鼠相比,通过以岩藻黄质口服预处理CCl(4)注射的大鼠,肝血红素加氧酶-1蛋白水平显着增加。 CCl(4)+岩藻黄质组注射CCl(4)后血红素加氧酶-1 mRNA表达高于CCl(4)组,尽管差异不显着。研究结果表明岩藻黄质通过血红素加氧酶-1诱导在CCl(4)诱导的急性肝损伤中减轻肝细胞凋亡。

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