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高脂饮食诱导仓鼠和小鼠血浆甘油三酯反应不同的机制:肝 MTP 和甘油三酯分泌的作用。

Mechanisms underlying different responses of plasma triglyceride to high-fat diets in hamsters and mice: roles of hepatic MTP and triglyceride secretion.

机构信息

Institute of Cardiovascular Sciences and Key Laboratory of Molecular Cardiovascular Sciences, Ministry of Education, Peking University Health Science Center, 38 Xueyuan Road, Haidian District, Beijing 100191, China.

出版信息

Biochem Biophys Res Commun. 2010 Aug 6;398(4):619-26. doi: 10.1016/j.bbrc.2010.05.114. Epub 2010 May 27.

Abstract

Hypertriglyceridemia, closely associated with insulin resistance, is induced on high-fat diets (HFD) in humans but not in mouse models. Mechanisms underlying this species difference are still unclear. Hamsters resemble humans in lipoprotein metabolism. Here by comparing the responses to HFD in hamsters and mice, we found that hepatic TG secretion, MTP expression and plasma free fatty acid (FFA) level were increased in hamsters on HFD feeding but decreased in mice. Although hepatic steatosis and de novo lipogenesis were induced by HFD feeding in both models, cholesterol biosynthesis was inhibited in mice but not in hamsters. Moreover, in insulin deficient state, HFD increased plasma TG level, hepatic TG secretion, MTP expression and plasma FFA level in both models. In summary, distinct changes of MTP expression, in correlation with hepatic TG secretion, underlie the opposite responses of plasma TG levels to high-fat diets in hamsters and mice. Furthermore, hepatic TG secretion and MTP expression seems to be associated with plasma FFA level and cholesterol biosynthesis but not hepatic steatosis or de novo lipogenesis.

摘要

高甘油三酯血症与胰岛素抵抗密切相关,可在人类的高脂肪饮食(HFD)中诱发,但在小鼠模型中则不会。这种物种差异的机制尚不清楚。仓鼠的脂蛋白代谢与人类相似。通过比较仓鼠和小鼠对 HFD 的反应,我们发现 HFD 喂养会增加仓鼠肝脏 TG 分泌、MTP 表达和血浆游离脂肪酸(FFA)水平,但会降低小鼠的这些指标。尽管 HFD 喂养在两种模型中均诱导肝脂肪变性和从头合成脂肪,但胆固醇生物合成在小鼠中受到抑制,而在仓鼠中则不受抑制。此外,在胰岛素缺乏状态下,HFD 会增加两种模型的血浆 TG 水平、肝脏 TG 分泌、MTP 表达和血浆 FFA 水平。综上所述,MTP 表达的变化与肝脏 TG 分泌密切相关,是导致仓鼠和小鼠对高脂肪饮食的血浆 TG 水平产生相反反应的基础。此外,肝脏 TG 分泌和 MTP 表达似乎与血浆 FFA 水平和胆固醇生物合成有关,但与肝脂肪变性或从头合成脂肪无关。

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