首页> 外文期刊>Diabetes >A Choline-Deficient Diet Exacerbates Fatty Liver but Attenuates Insulin Resistance and Glucose Intolerance in Mice Fed a High-Fat Diet.
【24h】

A Choline-Deficient Diet Exacerbates Fatty Liver but Attenuates Insulin Resistance and Glucose Intolerance in Mice Fed a High-Fat Diet.

机译:饲喂高脂饮食的胆碱缺乏饮食会加重脂肪肝,但会削弱胰岛素抵抗和葡萄糖耐量。

获取原文
获取原文并翻译 | 示例
       

摘要

Liver fat accumulation is proposed to link obesity and insulin resistance. To dissect the role of liver fat in the insulin resistance of diet-induced obesity, we altered liver fat using a choline-deficient diet. C57Bl/6 mice were fed a low-fat (10% of calories) or high-fat (45% of calories) diet for 8 weeks; during the final 4 weeks, diets were either choline deficient or choline supplemented. In choline replete animals, high-fat feeding induced weight gain, elevated liver triglycerides (171%), hyperinsulinemia, and glucose intolerance. Choline deficiency did not affect body or adipose depot weights but amplified liver fat accumulation with high-fat diet (281%, P < 0.01). However, choline deficiency lowered fasting plasma insulin (from 983 +/- 175 to 433 +/- 36 pmol/l, P < 0.01) and improved glucose tolerance on a high-fat diet. In mice on 30% fat diet, choline deficiency increased liver mRNA levels of the rate-limiting enzyme in phosphatidylcholine synthesis and of enzymes involved in free fatty acid esterification, without affecting those of de novo lipogenesis or fatty acid oxidation. We conclude that liver fat accumulation per se does not cause insulin resistance during high-fat feeding and that choline deficiency may shunt potentially toxic free fatty acids toward innocuous storage triglyceride in the liver.
机译:有人建议将肝脏脂肪积累与肥胖症和胰岛素抵抗联系起来。为了剖析肝脂肪在饮食诱导的肥胖症的胰岛素抵抗中的作用,我们使用胆碱缺乏饮食来改变肝脂肪。用低脂(10%卡路里)或高脂(45%卡路里)饮食喂养C57Bl / 6小鼠8周;在最后的4周内,饮食中胆碱缺乏或补充了胆碱。在胆碱丰富的动物中,高脂喂养会导致体重增加,肝甘油三酸酯升高(171%),高胰岛素血症和葡萄糖耐受不良。胆碱缺乏症不会影响人体或脂肪库的重量,但是在高脂饮食下会增加肝脂肪的积累(281%,P <0.01)。但是,胆碱缺乏会降低空腹血浆胰岛素(从983 +/- 175降至433 +/- 36 pmol / l,P <0.01),并改善高脂饮食对葡萄糖的耐受性。在30%脂肪饮食的小鼠中,胆碱缺乏会增加磷脂酰胆碱合成中限速酶和参与游离脂肪酸酯化的酶的肝脏mRNA水平,而不会影响从头脂肪生成或脂肪酸氧化的酶。我们得出的结论是,在高脂喂养期间,肝脏脂肪的积累本身不会引起胰岛素抵抗,胆碱缺乏可能将潜在的有毒游离脂肪酸分流到肝脏中无害的甘油三酸酯储存处。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号