Cowles Russell L, Lee Ji-Young, Gallaher Daniel D, Stuefer-Powell Cindy L, Carr Timothy P
Department of Nutritional Science and Dietetics, University of Nebraska, Lincoln 68583, USA.
J Nutr. 2002 Oct;132(10):3119-22. doi: 10.1093/jn/131.10.3119.
Dietary stearic acid (18:0) lowers plasma and liver cholesterol concentration by reducing intestinal cholesterol absorption. We tested the hypothesis that dietary 18:0 reduces cholesterol absorption by altering hepatic bile acid synthesis and gallbladder bile acid composition. Male Syrian hamsters were fed modified NIH-07 open formula diets, enriched (5 g/100 g diet) in one of the following fatty acids: 18:0, palmitic acid (16:0), trans fatty acids (18:1t), oleic acid (18:1c) or linoleic acid (18:2). After 18 wk, gallbladders were removed and bile acid composition determined by HPLC. The distribution of primary bile acids (mol/100 mol) was unaffected by treatment. In contrast, dietary 18:0 significantly reduced the proportion of hydrophobic secondary bile acids, resulting in a lower hydrophobicity index of the bile. These data suggest that reduced cholesterol absorption by dietary 18:0 is due, at least in part, to reduced cholesterol solubility. The data further suggest that 18:0 may have altered the microflora populations that synthesize secondary bile acids. Although cholesterol 7alpha-hydroxylase (CYP7A1) activity was significantly higher in hamsters fed 18:0 compared with 16:0, this finding is most likely due to increased fecal bile acid output in the 18:0 group rather than transcriptional regulation of CYP7A1 by 18:0 or specific bile acids.
膳食硬脂酸(18:0)通过减少肠道胆固醇吸收来降低血浆和肝脏胆固醇浓度。我们检验了这样一个假设,即膳食18:0通过改变肝脏胆汁酸合成和胆囊胆汁酸组成来降低胆固醇吸收。给雄性叙利亚仓鼠喂食改良的NIH - 07开放式配方饮食,其中富含(5 g/100 g饮食)以下脂肪酸之一:18:0、棕榈酸(16:0)、反式脂肪酸(18:1t)、油酸(18:1c)或亚油酸(18:2)。18周后,切除胆囊并通过高效液相色谱法测定胆汁酸组成。初级胆汁酸的分布(mol/100 mol)不受处理影响。相比之下,膳食18:0显著降低了疏水性次级胆汁酸的比例,导致胆汁的疏水性指数降低。这些数据表明,膳食18:0降低胆固醇吸收至少部分是由于胆固醇溶解度降低。数据进一步表明,18:0可能改变了合成次级胆汁酸的微生物菌群。尽管与喂食16:0的仓鼠相比,喂食18:0的仓鼠中胆固醇7α - 羟化酶(CYP7A1)活性显著更高,但这一发现很可能是由于18:0组粪便胆汁酸输出增加,而非18:0或特定胆汁酸对CYP7A1的转录调控。