Malewiak M I, Griglio S, Le Liepvre X
Metabolism. 1985 Jul;34(7):604-11. doi: 10.1016/0026-0495(85)90085-x.
The relationship between lipogenesis and ketogenesis and the concentration of malonyl coenzyme A (CoA) was investigated in hepatocytes from adult obese Zucker rats and their lean littermates fed either a control low-fat diet or a high-fat diet (30% lard in weight). With the control diet, lipogenesis--although strongly inhibited in the presence of either 1 mmol/L oleate, 10(-6) mol/L glucagon or 0.1 mmol/L TOFA (a hypolipidemic drug)--remained about fifteen-fold higher in the obese rats than in the lean rats. In contrast, ketogenesis under some conditions (oleate + TOFA) was not significantly lower (30%) as compared with the lean rats. After adaptation to the high-fat diet, lipogenesis was depressed fourfold in the lean rats and ninefold in the obese ones; however its magnitude remained significantly higher in the latter, namely at a value close to that measured in control-fed lean rats. Ketogenesis was comparable in lean and obese rats and much higher in the presence of 1 mmol/L oleate than of 0.3 mmol/L oleate, whereas lipogenesis did not vary with increasing oleate concentration in the medium. Acetyl-CoA carboxylase activity measured in liver homogenates was higher in the obese group, but was stepwise inhibited by increasing concentrations of oleyl-CoA regardless of the diet for both lean and obese rats, thus showing no abnormality of in vitro responsiveness to this inhibitor. With the control diet, hepatocyte malonyl-CoA levels were significantly higher in the obese rats, both in the basal state and after inhibition of lipogenesis by oleate and TOFA.(ABSTRACT TRUNCATED AT 250 WORDS)
研究了成年肥胖 Zucker 大鼠及其瘦的同窝仔鼠的肝细胞中脂肪生成、生酮作用与丙二酰辅酶 A(CoA)浓度之间的关系。这些大鼠分别喂食对照低脂饮食或高脂饮食(重量含 30%猪油)。对于对照饮食,尽管在存在 1 mmol/L 油酸、10⁻⁶ mol/L 胰高血糖素或 0.1 mmol/L TOFA(一种降血脂药物)时脂肪生成受到强烈抑制,但肥胖大鼠的脂肪生成仍比瘦大鼠高约 15 倍。相比之下,在某些条件下(油酸 + TOFA),肥胖大鼠的生酮作用与瘦大鼠相比降低并不显著(30%)。适应高脂饮食后,瘦大鼠的脂肪生成降低了 4 倍,肥胖大鼠降低了 9 倍;然而,肥胖大鼠的脂肪生成量仍显著高于瘦大鼠,即接近喂食对照饮食的瘦大鼠所测得的值。瘦大鼠和肥胖大鼠的生酮作用相当,在存在 1 mmol/L 油酸时比 0.3 mmol/L 油酸时高得多,而脂肪生成并不随培养基中油酸浓度的增加而变化。在肝脏匀浆中测得的乙酰辅酶 A 羧化酶活性在肥胖组中较高,但无论瘦大鼠还是肥胖大鼠,随着油酰辅酶 A 浓度的增加,该酶活性均逐步受到抑制,因此表明对该抑制剂的体外反应性无异常。对于对照饮食,肥胖大鼠肝细胞的丙二酰辅酶 A 水平在基础状态以及在油酸和 TOFA 抑制脂肪生成后均显著更高。(摘要截短于 250 字)