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对从瘦型和肥胖型 Zucker 大鼠分离的肝细胞进行脂肪酸合成、糖原代谢和糖异生的比较研究。

Comparative studies on fatty acid synthesis, glycogen metabolism, and gluconeogenesis by hepatocytes isolated from lean and obese Zucker rats.

作者信息

McCune S A, Durant P J, Jenkins P A, Harris R A

出版信息

Metabolism. 1981 Dec;30(12):1170-8. doi: 10.1016/0026-0495(81)90037-8.

Abstract

Hepatocytes isolated from genetically obese female Zucker rats and lean female Zucker rats were compared. Hepatocytes from fed obese rats exhibited greater rates of fatty acid synthesis, more extensive accumulation of lactate and pyruvate from their glycogen stores, increased rates of net glucose utilization but produced less ketone bodies from exogenous fatty acids and had lower citrate levels than hepatocytes from lean rats. Lipogenesis was not as sensitive to dibutyryl cyclic AMP (DBcAMP) inhibition in hepatocytes from obese rats but glycogenolysis was stimulated to the same extent by this nucleotide in both preparations. Ketogenesis was less sensitive to stimulation by DBcAMP in hepatocytes from obese rats. A difference in sensitivity of lipogenesis to DBcAMP was not found when lactate plus pyruvate was added to the incubation medium, suggesting that a greater rate of glycolysis by hepatocytes from obese rats accounts for their relative insensitivity to DBcAMP. Citrate levels were elevated by DBcAMP to a greater extent in hepatocytes from obese rats. Hepatocytes prepared from lean rats starved for 48 hr were glycogen depleted and lacked significant capacity for lipogenesis and glycogen synthesis. In contrast, hepatocytes isolated from starved obese rats retained considerable amounts of liver glycogen and exhibited detectable rates of lipogenesis and glycogen synthesis. Hepatocytes prepared from starved lean rats gave faster apparent rates of lactate gluconeogenesis than hepatocytes prepared from starved obese rats. Thus, hepatocytes prepared from obese Zucker rats are more glycogenic, glycolytic, and lipogenic but less ketogenic and glucogenic than hepatocytes prepared from lean rats.

摘要

对从遗传性肥胖雌性 Zucker 大鼠和瘦雌性 Zucker 大鼠中分离出的肝细胞进行了比较。喂食肥胖大鼠的肝细胞脂肪酸合成速率更高,从糖原储备中积累的乳酸和丙酮酸更多,净葡萄糖利用率增加,但从外源性脂肪酸产生的酮体较少,且柠檬酸盐水平低于瘦大鼠的肝细胞。肥胖大鼠肝细胞中的脂肪生成对二丁酰环磷酸腺苷(DBcAMP)抑制的敏感性较低,但在两种制剂中,这种核苷酸对糖原分解的刺激程度相同。肥胖大鼠肝细胞中的生酮作用对 DBcAMP 刺激的敏感性较低。当向孵育培养基中添加乳酸加丙酮酸时,未发现脂肪生成对 DBcAMP 的敏感性存在差异,这表明肥胖大鼠肝细胞较高的糖酵解速率导致了它们对 DBcAMP 的相对不敏感性。DBcAMP 使肥胖大鼠肝细胞中的柠檬酸盐水平升高幅度更大。饥饿 48 小时的瘦大鼠制备的肝细胞糖原耗尽,缺乏显著的脂肪生成和糖原合成能力。相比之下,从饥饿肥胖大鼠中分离出的肝细胞保留了大量肝糖原,并表现出可检测到的脂肪生成和糖原合成速率。饥饿瘦大鼠制备的肝细胞比饥饿肥胖大鼠制备的肝细胞乳酸糖异生的表观速率更快。因此,与从瘦大鼠制备的肝细胞相比,从肥胖 Zucker 大鼠制备的肝细胞糖原生成、糖酵解和脂肪生成能力更强,但生酮和糖异生能力较弱。

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