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首页> 外文期刊>BMC Genomics >C57Bl/6 N mice on a western diet display reduced intestinal and hepatic cholesterol levels despite a plasma hypercholesterolemia
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C57Bl/6 N mice on a western diet display reduced intestinal and hepatic cholesterol levels despite a plasma hypercholesterolemia

机译:尽管血浆高胆固醇血症,但采用西式饮食的C57Bl / 6 N小鼠显示出降低的肠和肝胆固醇水平

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Background Small intestine and liver greatly contribute to whole body lipid, cholesterol and phospholipid metabolism but to which extent cholesterol and phospholipid handling in these tissues is affected by high fat Western-style obesogenic diets remains to be determined. Methods We therefore measured cholesterol and phospholipid concentration in intestine and liver and quantified fecal neutral sterol and bile acid excretion in C57Bl/6 N mice fed for 12 weeks either a cholesterol-free high carbohydrate control diet or a high fat Western diet containing 0.03% (w/w) cholesterol. To identify the underlying mechanisms of dietary adaptations in intestine and liver, changes in gene expression were assessed by microarray and qPCR profiling, respectively. Results Mice on Western diet showed increased plasma cholesterol levels, associated with the higher dietary cholesterol supply, yet, significantly reduced cholesterol levels were found in intestine and liver. Transcript profiling revealed evidence that expression of numerous genes involved in cholesterol synthesis and uptake via LDL, but also in phospholipid metabolism, underwent compensatory regulations in both tissues. Alterations in glycerophospholipid metabolism were confirmed at the metabolite level by phospolipid profiling via mass spectrometry. Conclusions Our findings suggest that intestine and liver react to a high dietary fat intake by an activation of de novo cholesterol synthesis and other cholesterol-saving mechanisms, as well as with major changes in phospholipid metabolism, to accommodate to the fat load.
机译:背景技术小肠和肝脏极大地促进了体内脂质,胆固醇和磷脂的代谢,但是在这些组织中胆固醇和磷脂的处理受高脂西式肥胖饮食影响的程度尚待确定。方法因此,我们测量了无胆固醇高碳水化合物对照饮食或高脂西方饮食(含0.03%(0.04%))的C57Bl / 6 N小鼠喂养12周后的肠道和肝脏中胆固醇和磷脂的浓度,并定量了粪便中性固醇和胆汁酸的排泄。 w / w)胆固醇。为了确定肠道和肝脏饮食适应的潜在机制,分别通过微阵列和qPCR谱评估基因表达的变化。结果西方饮食的小鼠血浆胆固醇水平升高,与饮食中胆固醇的供应增加有关,但是在肠道和肝脏中胆固醇水平却明显降低。转录谱分析揭示了证据,表明参与胆固醇合成和通过低密度脂蛋白摄取以及磷脂代谢的许多基因的表达均在两个组织中受到补偿性调节。通过质谱分析通过磷脂轮廓分析,在代谢产物水平确认了甘油磷脂代谢的变化。结论我们的发现表明,肠道和肝脏通过激活从头胆固醇合成和其他节省胆固醇的机制对饮食中的高脂肪摄入作出反应,以及磷脂代谢的重大变化来适应脂肪负荷。

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