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发育中大鼠肝脏中脂肪酸用于酮体和复合脂质合成的相对利用率。

Relative utilization of fatty acids for synthesis of ketone bodies and complex lipids in the liver of developing rats.

作者信息

Yeh Y Y, Streuli V L, Zee P

出版信息

Lipids. 1977 Apr;12(4):367-74. doi: 10.1007/BF02533640.

Abstract

The regulation of hepatic ketogenesis, as related to the metabolism of fatty acids through oxidative and synthetic pathways, was studied in developing rats. [1-14C] palmitate was used as a substrate to determine the proportions of free fatty acids utilized for the production of ketone bodies, CO2 and complex lipids. Similar developmental patterns of hepatic ketogenesis were obtained by measuring the production of either [14C] acetoacetate from exogenous [1-14C] palmitate or the sum of unlabeled acetoacetate and beta-hydroxybutyrate from endogenous fatty acids. The production of total ketone bodies was low during the late fetal stage and at birth, but increased rapidly to a miximum value within 24 hr after brith. The maximal ketogenic capacity appeared to be maintained for the first 10 days of life. 14CO2 production from [1-14C] palmitate increased by two- to fourfold during the suckling period, from its initial low rate seen at birth. The capacity for synthesis of total complex lipids was low at birth and had increased by day 3 to a maximal value, which was comparable to that of adult fed rats. The high lipogenic capacity lasted throughout the remaining suckling period. When ketogenesis was inhibited by 4-pentenoic acid, the rate of synthesis of complex lipids did not increase despite an increase in unutilized fatty acids. During the mid-suckling period, approximately equal amounts of [1-14C] palmitate were utilized for the synthesis of ketone plus CO2 and for complex lipid synthesis. By contrast, in adult fed rats, the incorporation of fatty acids into complex lipids was four times higher than that of ketone plus CO2. These observations suggest that stimulated hepatic ketogenesis in suckling rats results from the rapid oxidation of fatty acids and consequent increased production of acetyl CoA, but not from impaired capacity for synthesis of complex lipids.

摘要

在发育中的大鼠中,研究了与脂肪酸通过氧化和合成途径代谢相关的肝脏生酮作用的调节。[1-14C]棕榈酸酯用作底物,以确定用于生成酮体、二氧化碳和复合脂质的游离脂肪酸比例。通过测量外源性[1-14C]棕榈酸酯生成的[14C]乙酰乙酸或内源性脂肪酸生成的未标记乙酰乙酸和β-羟基丁酸的总和,获得了相似的肝脏生酮发育模式。总酮体的生成在胎儿后期和出生时较低,但在出生后24小时内迅速增加至最大值。最大生酮能力在出生后的前10天似乎保持不变。[1-14C]棕榈酸酯生成的14CO2在哺乳期从出生时的初始低速率增加了两到四倍。总复合脂质的合成能力在出生时较低,到第3天增加到最大值,这与成年喂食大鼠相当。高脂质生成能力在整个剩余哺乳期持续存在。当生酮作用被4-戊烯酸抑制时,尽管未利用的脂肪酸增加,但复合脂质的合成速率并未增加。在哺乳中期,大约等量的[1-14C]棕榈酸酯用于合成酮体加二氧化碳和复合脂质合成。相比之下,在成年喂食大鼠中,脂肪酸掺入复合脂质的量比酮体加二氧化碳高四倍。这些观察结果表明,哺乳大鼠肝脏生酮作用的增强是由于脂肪酸的快速氧化以及随之而来的乙酰辅酶A生成增加,而不是由于复合脂质合成能力受损。

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