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禁食-再喂养及膳食亚油酸对适应纯化饮食大鼠肝脏葡萄糖-6-磷酸脱氢酶和磷脂脂肪酸组成的影响。

Influence of fasting-refeeding and dietary linoleate on liver glucose-6-phosphate dehydrogenase and phospholipid fatty acid composition in rats adapted to a purified diet.

作者信息

Williams M A, Tinoco J, Ojakian M A, Clark L

出版信息

Lipids. 1977 Apr;12(4):386-92. doi: 10.1007/BF02533643.

DOI:10.1007/BF02533643
PMID:857113
Abstract

Responses to refeeding after fasting were studied in male rats fed a purified casein-sucrose diet containing 5% safflower oil. After a 48 hr fast, the rats were fed either the same diet or the same diet minus oil (fat-free diet). These experiments were designed to distinguish changes due to fasting and refeeding alone without a change of diet from those changes caused by refeeding a diet of different composition. In the first experiment, rats were refed for 3 or 7 days. In rats refed either diet, liver glucose-6-phosphate dehydrogenase (G6PD) activity was elevated above refasting levels, but after 7 days, activity in rats refed the 5% safflower oil diet was significantly lower than in those refed the fat-free diet. The amount of liver arachidonate in rats refed the safflower oil diet was the same during refeeding as before fasting. In the second experiment, rats were refed the fat-free diet for 1, 2, 3, or 7 days. Liver G6PD and fatty acid synthetase were measured, as well as fatty acids in liver total lipids and phospholipids. G6PD activity increased above prefasting levels after one day refeeding and continued to increase for 7 days. Fatty acid synthetase activity increased for the first 3 days of refeeding, with no additional increase after 7 days. In all rats refed the fat-free diet, the proportions of arachidonate and linoleate in liver phospholipids diminished with time, and eicosatrienoate appeared. These results show that (a) maintenance of liver phospholipid arachidonate did not prevent increased G6PD activity in early refeeding, but the elevated G6PD activity later declined when phospholipid arachidonate was maintained by feeding a source of linoleate; (b) the metabolic state of fasted-refed rats had not returned to prefasting conditions even after 7 days of refeeding a linoleate-rich diet to which the rats were adapted before fasting.

摘要

对禁食后再喂食的反应在喂食含5%红花油的纯化酪蛋白 - 蔗糖饮食的雄性大鼠中进行了研究。禁食48小时后,给大鼠喂食相同饮食或相同但不含油的饮食(无脂饮食)。这些实验旨在区分仅由禁食和再喂食引起的变化(饮食无变化)与由喂食不同成分饮食引起的变化。在第一个实验中,大鼠再喂食3天或7天。在再喂食任何一种饮食的大鼠中,肝脏葡萄糖 - 6 - 磷酸脱氢酶(G6PD)活性高于再禁食水平,但7天后,再喂食含5%红花油饮食的大鼠的活性显著低于再喂食无脂饮食的大鼠。再喂食红花油饮食的大鼠肝脏花生四烯酸的量在再喂食期间与禁食前相同。在第二个实验中,大鼠再喂食无脂饮食1、2、3或7天。测量了肝脏G6PD和脂肪酸合成酶,以及肝脏总脂质和磷脂中的脂肪酸。再喂食一天后,G6PD活性高于禁食前水平,并持续增加7天。脂肪酸合成酶活性在再喂食的前3天增加,7天后没有进一步增加。在所有再喂食无脂饮食的大鼠中,肝脏磷脂中花生四烯酸和亚油酸的比例随时间减少,并且出现了二十碳三烯酸。这些结果表明:(a)肝脏磷脂花生四烯酸的维持并不能阻止早期再喂食时G6PD活性的增加,但当通过喂食亚油酸来源维持磷脂花生四烯酸时,升高的G6PD活性随后下降;(b)即使在禁食前使大鼠适应富含亚油酸的饮食再喂食7天后,禁食 - 再喂食大鼠的代谢状态也未恢复到禁食前状态。

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引用本文的文献

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本文引用的文献

1
FATTY ACID SYNTHESIS DURING FAT-FREE REFEEDING OF STARVED RATS.饥饿大鼠无脂再喂养期间的脂肪酸合成
J Lipid Res. 1965 Jan;6:63-74.
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Enzymatic and metabolic adaptations. I. Changes in intact rats subjected to dietary modifications.酶促与代谢适应性。I. 饮食改变对完整大鼠的影响。
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Metabolism of glucose-1-C-14 and glucose-6-C-14 by liver slices of refed rats.再喂食大鼠肝脏切片对1 - C - 14葡萄糖和6 - C - 14葡萄糖的代谢
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De novo synthesis of fatty acid in perfused rat liver as a determinant of plasma lipoprotein production.灌注大鼠肝脏中脂肪酸的从头合成作为血浆脂蛋白产生的决定因素。
Arch Biochem Biophys. 1967 Nov;122(2):362-9. doi: 10.1016/0003-9861(67)90206-8.
5
Studies on lipogenesis in vivo. Lipogenesis during extended periods of re-feeding after starvation.体内脂肪生成的研究。饥饿后长期再喂养期间的脂肪生成。
Biochem J. 1968 Jan;106(2):345-53. doi: 10.1042/bj1060345.
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Selective dampening of lipogenic enzymes of liver by exogenous polyunsaturated fatty acids.外源性多不饱和脂肪酸对肝脏生脂酶的选择性抑制作用。
Biochem Biophys Res Commun. 1970 Jan 6;38(1):9-15. doi: 10.1016/0006-291x(70)91076-4.
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Dietary unsaturated fatty acids and liver fatty acid synthetase in rats.大鼠的膳食不饱和脂肪酸与肝脏脂肪酸合成酶
Biochim Biophys Acta. 1969 Dec 17;187(4):573-5. doi: 10.1016/0005-2760(69)90055-1.
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Phospholipid metabolism in endoplasmic reticular membranes in rats fed high-carbohydrate diet.高碳水化合物饮食喂养大鼠内质网膜中的磷脂代谢
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