Ito Yoshiya, Abril Edward R, Bethea Nancy W, McCuskey Margaret K, McCuskey Robert S
Department of Cell Biology and Anatomy, College of Medicine, University of Arizona, Tucson, Arizona 85724-5044, USA.
Microcirculation. 2006 Jan;13(1):19-27. doi: 10.1080/10739680500383423.
To determine whether hepatic steatosis is susceptible to acetaminophen (APAP) hepatotoxicity.
Male C57Bl/6 mice were fed a "Western-style" diet (high fat and high carbohydrate) for 4 months to develop severe hepatic steatosis with mild increases in alanine aminotransferase (ALT) levels. These were compared to mice fed a standard chow diet.
Treatment with APAP (300 mg/kg, orally) to mice fed a regular chow increased ALT levels (519-fold) and caused hepatic centrilobular injury at 6 h. APAP increased hepatic cytochrome-P (CYP)-2E1 mRNA levels (17-fold). In vivo microscopic studies showed that APAP caused a 30% decrease in sinusoidal perfusion and the infiltration of red blood cells into the space of Disse. Electron microscopy demonstrated that numerous gaps were formed in sinusoidal endothelial cells. Mice fed the "Western-style" diet were protected from APAP hepatotoxicity as evidenced by 89% decrease in ALT levels and less centrilobular injury, which was associated with 42% decrease in CYP2E1 mRNA levels. The APAP-induced liver microcirculatory dysfunction was minimized in mice fed the "Western-style" diet.
These results suggest that hepatic steatosis elicited by the "Western-style" diet attenuated APAP-induced hepatotoxicity by inhibiting CYP2E1 induction and by minimizing sinusoidal endothelial cell injury, leading to protection of liver microcirculation.
确定肝脂肪变性是否易患对乙酰氨基酚(APAP)肝毒性。
雄性C57Bl/6小鼠喂食“西式”饮食(高脂肪和高碳水化合物)4个月,以发展为严重肝脂肪变性,丙氨酸转氨酶(ALT)水平轻度升高。将这些小鼠与喂食标准普通饲料的小鼠进行比较。
对喂食普通饲料的小鼠口服给予APAP(300mg/kg),6小时时ALT水平升高(519倍)并导致肝小叶中央损伤。APAP使肝细胞色素P(CYP)-2E1 mRNA水平升高(17倍)。体内显微镜研究表明,APAP使肝血窦灌注减少30%,红细胞浸润到狄氏间隙。电子显微镜显示肝血窦内皮细胞形成大量间隙。喂食“西式”饮食的小鼠对APAP肝毒性具有保护作用,ALT水平降低89%,肝小叶中央损伤减轻,这与CYP2E1 mRNA水平降低42%有关。喂食“西式”饮食的小鼠中,APAP诱导的肝脏微循环功能障碍降至最低。
这些结果表明,“西式”饮食引起的肝脂肪变性通过抑制CYP2E1诱导和使肝血窦内皮细胞损伤最小化,减轻了APAP诱导的肝毒性,从而保护了肝脏微循环。