首页> 外文期刊>American Journal of Physiology >Impact of starvation-refeeding on kinetics and protein expression of trout liver NADPH-production systems.
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Impact of starvation-refeeding on kinetics and protein expression of trout liver NADPH-production systems.

机译:饥饿补给对鳟鱼肝脏NADPH生产系统动力学和蛋白质表达的影响。

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摘要

Herein we report on the kinetic and protein expression of glucose-6-phosphate dehydrogenase (G6PDH), 6-phosphogluconate dehydrogenase, and malic enzyme (ME) in the liver of the trout (Oncorhynchus mykiss) during a long-term starvation-refeeding cycle. Starvation significantly depressed the activity of these enzymes by almost 60%, without changing the Michaelis constant. The time response to this nutritional stimulus increased with fish weight. The sharp decline in G6PDH and ME activities was due to a specific protein-repression phenomenon, as demonstrated by molecular and immunohistochemical analyses. Also, the dimeric banding pattern of liver G6PDH shifted from the fully reduced and partially oxidized forms, predominant in control, to a fully oxidized form, more sensitive to proteolytic inactivation. Refeeding caused opposite effects in both protein concentration and enzyme activities of about twice the control values in the first stages, later reaching the normal enzyme activity levels. Additionally, the partially oxidized form of G6PDH increased. The kinetics of these enzymes were examined in relation to the various metabolic roles of NADPH. These results clearly indicate that trout liver undergoes protein repression-induction processes under these two contrasting nutritional conditions.
机译:在此,我们报道了在长期饥饿-重新喂养周期中,鳟鱼肝脏中的6-磷酸葡萄糖脱氢酶(G6PDH),6-磷酸葡萄糖脱氢酶和苹果酸酶(ME)的动力学和蛋白质表达。 。饥饿使这些酶的活性降低了近60%,而没有改变米氏常数。随着鱼的体重,对这种营养刺激的时间响应增加。 G6PDH和ME活性的急剧下降是由于一种特定的蛋白抑制现象,如分子和免疫组织化学分析所证明的。同样,肝脏G6PDH的二聚体条带化模式从对控制为主的完全还原和部分氧化形式转变为对蛋白水解失活更加敏感的完全氧化形式。再次进食对蛋白质浓度和酶活性均产生相反的影响,约为最初阶段控制值的两倍,后来达到正常的酶活性水平。此外,G6PDH的部分氧化形式增加。这些酶的动力学与NADPH的各种代谢作用有关。这些结果清楚地表明,在这两种相反的营养条件下,鳟鱼肝经历了蛋白质抑制诱导过程。

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