Sonoyama K, Nishikawa H, Kiriyama S, Niki R
Laboratory of Food Biochemistry, Faculty of Agriculture, Hokkaido-University, Sapporo, Japan.
J Nutr Sci Vitaminol (Tokyo). 1994 Aug;40(4):343-52. doi: 10.3177/jnsv.40.343.
We recently reported that cholestyramine (a bile acid sequestrant) lowered ileal apolipoprotein A-I mRNA level in rats. To obtain further information about this phenomenon, in this study, we investigated whether bile diversion lowers apolipoprotein A-I mRNA level in the ileum of rats. Bile-diverted rats were fed a diet with no added Na taurocholate (control diet) or with 0.4% Na taurocholate for 7 days. Sham-operated rats were also fed the control diet for the same period. Northern blot analysis revealed that the relative concentrations of jejunal apolipoprotein A-I and A-IV mRNA at the end of experimental period did not differ between groups while ileal apolipoprotein A-I and A-IV mRNA concentrations were significantly lower in bile-diverted rats fed the control and Na taurocholate-containing diets than in sham-operated rats. Plasma total and HDL cholesterol concentrations were the same in all groups. Relative concentration of apolipoprotein A-I in plasma also did not change. These results suggest that the bile plays an important role in ileal apolipoprotein gene expression at the pretranslational stage, but it is still unclear whether the effector is the bile acid or not. The unchanged concentration of plasma apolipoprotein A-I may have resulted from the constant secretion independent of synthesis in the intestine or the larger contribution from the liver which is another principal site for apolipoprotein A-I expression.
我们最近报道,消胆胺(一种胆汁酸螯合剂)可降低大鼠回肠载脂蛋白A-I的mRNA水平。为了获得关于这一现象的更多信息,在本研究中,我们调查了胆汁转流是否会降低大鼠回肠中载脂蛋白A-I的mRNA水平。给胆汁转流的大鼠喂食不含牛磺胆酸钠的饮食(对照饮食)或含0.4%牛磺胆酸钠的饮食7天。假手术大鼠在同一时期也喂食对照饮食。Northern印迹分析显示,在实验期结束时,空肠载脂蛋白A-I和A-IV的mRNA相对浓度在各组之间没有差异,而喂食对照饮食和含牛磺胆酸钠饮食的胆汁转流大鼠的回肠载脂蛋白A-I和A-IV的mRNA浓度显著低于假手术大鼠。所有组的血浆总胆固醇和高密度脂蛋白胆固醇浓度相同。血浆中载脂蛋白A-I的相对浓度也没有变化。这些结果表明,胆汁在翻译前阶段的回肠载脂蛋白基因表达中起重要作用,但尚不清楚效应物是否为胆汁酸。血浆载脂蛋白A-I浓度不变可能是由于其分泌恒定,与肠道合成无关,或者是由于肝脏(载脂蛋白A-I表达的另一个主要部位)的贡献更大。