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饥饿时由于内质网吡啶核苷酸的氧化转移使受体前糖皮质激素激活能力降低。

Decreased prereceptorial glucocorticoid activating capacity in starvation due to an oxidative shift of pyridine nucleotides in the endoplasmic reticulum.

机构信息

Department of Medical Chemistry, Molecular Biology and Pathobiochemistry, Semmelweis University, 1444 Budapest, Hungary.

出版信息

FEBS Lett. 2010 Nov 19;584(22):4703-8. doi: 10.1016/j.febslet.2010.10.053. Epub 2010 Oct 28.

Abstract

Redox state of pyridine nucleotides of the endoplasmic reticulum (ER) lumen was determined in different nutritional conditions. NADPH-dependent cortisone reduction and NADP(+)-dependent cortisol oxidation were measured in rat liver microsomes, by utilizing the luminal 11β-hydroxysteroid dehydrogenase type 1 activity. Cortisone reduction decreased, while cortisol oxidation increased during onward starvation, showing that the luminal NADPH/NADP(+) ratio was substantially decreased. Cortisone or metyrapone addition caused a smaller decrease in NADPH fluorescence in microsomes from starved rats. The results demonstrate that nutrient supply is mirrored by the redox state of ER luminal pyridine nucleotides.

摘要

内质网腔吡啶核苷酸的氧化还原状态在不同的营养条件下进行了测定。利用腔 11β-羟甾类脱氢酶 1 的活性,在大鼠肝微粒体中测定了 NADPH 依赖性可的松还原和 NADP(+)依赖性皮质醇氧化。在继续饥饿过程中,可的松还原减少,而皮质醇氧化增加,表明腔 NADPH/NADP(+) 比值显著降低。可的松或美替拉酮的添加导致来自饥饿大鼠的微粒体中 NADPH 荧光的减少较小。结果表明,内质网腔吡啶核苷酸的氧化还原状态反映了营养供应情况。

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