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含不饱和脂肪饮食对大鼠肝细胞脂肪酸和胆固醇合成影响的昼夜变化。

Diurnal variations in the effects of an unsaturated-fat-containing diet on fatty acid and cholesterol synthesis in rat hepatocytes.

作者信息

Gibbons G F, Pullinger C R

出版信息

Biochem J. 1986 Nov 1;239(3):617-23. doi: 10.1042/bj2390617.

Abstract

Rats were fed ad libitum on either a standard high-carbohydrate diet, or a standard diet supplemented with 15% corn oil. Hepatocytes were prepared either during the light phase (L2-hepatocytes) or during the dark phase (D6-hepatocytes) of the diurnal cycle. In hepatocytes from rats fed on the fat-containing diet, fatty acid synthesis (lipogenesis) was suppressed to a much greater extent at D6 than at L2. The magnitude of the increase in plasma-free fatty acid concentration was similar at the two times of day. The rate of cholesterol synthesis was also significantly suppressed in the D6- but not in the L2-hepatocytes. This differential inhibition resulted in the abolition of the normal diurnal rhythm of cholesterogenesis. The initial activity of 3-hydroxy-3-methylglutaryl-CoA reductase in hepatocytes was also suppressed by corn-oil feeding at D6 but not at L2. In D6-hepatocytes, the inhibitory effect of the high-fat diet on the conversion of lactate into cholesterol and fatty acids was greater than that on total carbon flux into these substances for all endogenous sources. Despite this, under these conditions a high concentration of lactate and pyruvate resulted in a several-fold stimulation of total carbon flux into fatty acids. In hepatocytes prepared at L2, fat-feeding had little effect on the degree of stimulation of lipogenesis by insulin or inhibition by glucagon. However, at D6, fat-feeding blunted the response of lipogenesis to both these hormones.

摘要

大鼠随意进食标准高碳水化合物饮食或添加15%玉米油的标准饮食。在昼夜周期的光照阶段(L2肝细胞)或黑暗阶段(D6肝细胞)制备肝细胞。在喂食含脂肪饮食的大鼠的肝细胞中,脂肪酸合成(脂肪生成)在D6时比在L2时受到更大程度的抑制。血浆游离脂肪酸浓度升高的幅度在一天中的这两个时间相似。胆固醇合成速率在D6肝细胞中也受到显著抑制,但在L2肝细胞中未受抑制。这种差异抑制导致胆固醇生成的正常昼夜节律消失。喂食玉米油在D6时抑制了肝细胞中3-羟基-3-甲基戊二酰辅酶A还原酶的初始活性,但在L2时未抑制。在D6肝细胞中,高脂饮食对乳酸转化为胆固醇和脂肪酸的抑制作用大于对所有内源性来源的这些物质的总碳通量的抑制作用。尽管如此,在这些条件下,高浓度的乳酸和丙酮酸导致总碳通量向脂肪酸的刺激增加了几倍。在L2制备的肝细胞中,喂食脂肪对胰岛素刺激脂肪生成或胰高血糖素抑制脂肪生成的程度影响很小。然而,在D6时,喂食脂肪减弱了脂肪生成对这两种激素的反应。

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