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肥胖型 Zucker 大鼠肝细胞中利用 14C 乳酸生成脂肪。白蛋白结合油酸的作用。

Lipogenesis from U14C lactate in obese Zucker rat hepatocytes. Effect of albumin-bound oleate.

作者信息

Porquet D, Serbource-Goguel N, Durand G, Maccario J, Féger J, Agneray J

出版信息

Life Sci. 1984 Sep 10;35(11):1213-9. doi: 10.1016/0024-3205(84)90193-0.

Abstract

Lipogenesis from U(14C) lactate was studied in hepatocytes isolated from obese Zucker rats (fa/fa) their lean littermates (Fa/?) and Sprague Dawley rats. The distribution of radioactive carbon between the glycerol and the fatty acid moieties of the acylglycerols were studied. Radioactive lactate was better utilized for glycerol formation than it was for fatty acid formation in the obese rats. However, when oleate was added to the hepatocytic incubation medium, radioactive lactate was preferentially incorporated into the fatty acid moiety of the acylglycerols. Zucker obesity classified as a "metabolic obesity" by Meyer (1) depends upon abnormalities in carbohydrate metabolism associated with increased lipogenesis. This might be explained by biochemical shifts in the utilization of nutrients (2). Among the nutrients, lactate seems to be a better source of carbon than glucose for lipid synthesis (3). It has been shown that there is an increased hepatic portal blood concentration of lactate several hours after eating: about 4 mM in Wistar rats (4) and 10-15 mM in obese Zucker rats (3). We are interested in determinating the incorporation of carbon from lactate either into glycerol or into fatty acyl moieties of hepatic acylglycerols, and in determining the influence of exogenous fatty acids on acylglycerol synthesis, since a high level of circulating fatty acids in Zucker obese rats has been reported (5). Our purpose was to determine the incorporation of lactate into glycerol and fatty acyl moieties of acylglycerols, under the influence of oleate. Hepatocytes were isolated from ad libitum fed obese Zucker rats (fa/fa), their lean littermates (Fa/?) and Sprague-Dawley rats (SD). Incorporation of lactate was studied for three hours, in order to exclude short-term regulation effects and to allow oleate to be distributed into all cellular compartments.

摘要

研究了从肥胖 Zucker 大鼠(fa/fa)、其瘦的同窝大鼠(Fa/?)和 Sprague Dawley 大鼠分离出的肝细胞中,U(14C)乳酸的脂肪生成情况。研究了酰基甘油的甘油和脂肪酸部分之间放射性碳的分布。在肥胖大鼠中,放射性乳酸用于甘油形成比用于脂肪酸形成更好。然而,当向肝细胞孵育培养基中添加油酸时,放射性乳酸优先掺入酰基甘油的脂肪酸部分。Meyer(1)将 Zucker 肥胖归类为“代谢性肥胖”,这取决于与脂肪生成增加相关的碳水化合物代谢异常。这可能由营养物质利用的生化变化来解释(2)。在营养物质中,乳酸似乎比葡萄糖更适合作为脂质合成的碳源(3)。已经表明,进食后数小时肝门静脉血中乳酸浓度会升高:Wistar 大鼠约为 4 mM(4),肥胖 Zucker 大鼠为 10 - 15 mM(3)。我们感兴趣的是确定乳酸中的碳掺入肝酰基甘油的甘油或脂肪酰部分的情况,以及确定外源性脂肪酸对酰基甘油合成的影响,因为已有报道 Zucker 肥胖大鼠中循环脂肪酸水平较高(5)。我们的目的是确定在油酸影响下乳酸掺入酰基甘油的甘油和脂肪酰部分的情况。从自由进食的肥胖 Zucker 大鼠(fa/fa)、其瘦的同窝大鼠(Fa/?)和 Sprague-Dawley 大鼠(SD)中分离肝细胞。研究了乳酸掺入情况持续三小时,以排除短期调节效应并使油酸分布到所有细胞区室。

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