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喂食和饥饿大鼠肝细胞中胆固醇生成速率的昼夜变化:体外前体和胰腺激素的影响

Diurnal changes in the rate of cholesterogenesis in hepatocytes from fed and starved rats: effects of precursors and pancreatic hormones in vitro.

作者信息

Björnsson O G, Pullinger C R, Gibbons G F

出版信息

Arch Biochem Biophys. 1985 Apr;238(1):135-45. doi: 10.1016/0003-9861(85)90149-3.

Abstract

The activity of 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMG-CoA reductase) varied with a diurnal periodicity in hepatocytes prepared at different times from rats accustomed to a controlled feeding and lighting schedule. The rates of sterol synthesis varied in a similar manner but the maximum rate was not synchronous with maximum HMG-CoA reductase activity. The diurnal increase in HMG-CoA reductase activity and sterol synthesis rate started before food was offered to donor animals. Neither insulin nor glucagon had any effect on the diurnal pattern of hepatic sterol synthesis in vitro. Pyruvate inhibited sterol synthesis in hepatocytes prepared during the feeding period but had no effect at other times of day. When food was withheld from donor animals at the beginning of the normal feeding period both HMG-CoA reductase activity and the rate of sterol synthesis rapidly decreased. During this period neither insulin nor lipogenic substrates, alone or in combination, were able to restore the rates of sterol synthesis to normal values. In hepatocytes prepared from animals starved for a longer period (43 h) the decrease in the activity of HMG-CoA reductase was much less than that in the rate of sterol synthesis. In contrast to hepatocytes from fed or short-term-starved animals, the rate of sterol synthesis in these hepatocytes could be increased by glucose or pyruvate.

摘要

在按照控制饮食和光照时间表饲养的大鼠不同时间制备的肝细胞中,3-羟基-3-甲基戊二酰辅酶A还原酶(HMG-CoA还原酶)的活性呈现昼夜周期性变化。固醇合成速率也以类似方式变化,但最大速率与HMG-CoA还原酶的最大活性并不同步。HMG-CoA还原酶活性和固醇合成速率的昼夜增加在向供体动物投喂食物之前就开始了。胰岛素和胰高血糖素对体外肝脏固醇合成的昼夜模式均无影响。丙酮酸抑制在进食期制备的肝细胞中的固醇合成,但在一天中的其他时间没有影响。在正常进食期开始时不给供体动物喂食,HMG-CoA还原酶活性和固醇合成速率均迅速下降。在此期间,单独或联合使用胰岛素和生脂底物均无法将固醇合成速率恢复到正常值。在饥饿较长时间(43小时)的动物制备的肝细胞中,HMG-CoA还原酶活性的下降远小于固醇合成速率的下降。与喂食或短期饥饿动物的肝细胞不同,这些肝细胞中的固醇合成速率可被葡萄糖或丙酮酸提高。

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