Larter Claire Z, Yeh Matthew M, Williams Jacqueline, Bell-Anderson Kim S, Farrell Geoffrey C
ANU Medical School, Australian National University at The Canberra Hospital, Canberra, ACT, Australia.
J Hepatol. 2008 Sep;49(3):407-16. doi: 10.1016/j.jhep.2008.03.026. Epub 2008 Apr 30.
BACKGROUND/AIMS: In these studies, we tested the hypothesis that increased lipid intake would exacerbate the severity of nutritional steatohepatitis.
C57Bl/6J mice were fed methionine-and-choline deficient (MCD) diets containing 20% (high) or 5% (low) fat by weight for 3 weeks and compared to lipid-matched controls.
MCD feeding increased serum ALT levels and induced hepatic steatosis, lobular inflammation and ballooning degeneration of hepatocytes, irrespective of dietary fat content. Hepatic triglyceride accumulation was similar between high and low-fat MCD-fed mice, but lipoperoxide levels were approximately 3-fold higher in the high-fat MCD-fed animals. Serum adiponectin levels increased in MCD-fed mice, although to a lesser extent in high-fat fed animals. AMPK phosphorylation was correspondingly increased in muscle of MCD-fed mice, but hepatic AMPK phosphorylation decreased, and there was little evidence of PPAR alpha activation, suggesting impaired adiponectin action in the livers of MCD-fed animals. Hepatocyte PPAR gamma mRNA levels increased in MCD-fed mice, and were associated with increased aP2 expression, indicating adipogenic transformation of hepatocytes.
Increased dietary lipid intake did not alter steatohepatitis severity in MCD-fed mice despite increased lipoperoxide accumulation. Instead, steatohepatitis was associated with impaired hepatic adiponectin action, and adipogenic transformation of hepatocytes in both low and high-fat MCD-fed mice.
背景/目的:在这些研究中,我们检验了以下假设,即增加脂质摄入会加重营养性脂肪性肝炎的严重程度。
给C57Bl/6J小鼠喂食蛋氨酸和胆碱缺乏(MCD)饮食,其中脂肪含量按重量计为20%(高)或5%(低),持续3周,并与脂质匹配的对照组进行比较。
无论饮食脂肪含量如何,MCD喂养均会增加血清ALT水平,并诱导肝脂肪变性、小叶炎症和肝细胞气球样变性。高脂和低脂MCD喂养的小鼠肝脏甘油三酯积累相似,但高脂MCD喂养的动物中脂过氧化物水平约高3倍。MCD喂养的小鼠血清脂联素水平升高,尽管在高脂喂养的动物中升高程度较小。MCD喂养的小鼠肌肉中AMPK磷酸化相应增加,但肝脏AMPK磷酸化降低,且几乎没有PPARα激活的证据,这表明MCD喂养的动物肝脏中脂联素作用受损。MCD喂养的小鼠肝细胞PPARγ mRNA水平升高,并与aP2表达增加相关,表明肝细胞发生脂肪生成转化。
尽管脂过氧化物积累增加,但增加饮食脂质摄入并未改变MCD喂养小鼠的脂肪性肝炎严重程度。相反,脂肪性肝炎与肝脏脂联素作用受损以及低脂和高脂MCD喂养小鼠肝细胞的脂肪生成转化有关。