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在C57BL/KsJ-db/db小鼠中,肝脏11β-羟基类固醇脱氢酶1型的mRNA和酶活性升高。

MRNA and enzyme activity of hepatic 11beta-hydroxysteroid dehydrogenase type 1 are elevated in C57BL/KsJ-db/db mice.

作者信息

Aoki K, Homma M, Hirano T, Oka K, Satoh S, Mukasa K, Ito S, Sekihara H

机构信息

The Third Department of Internal Medicine, Yokohama City University School of Medicine, Yokohama, Japan.

出版信息

Life Sci. 2001 Oct 12;69(21):2543-9. doi: 10.1016/s0024-3205(01)01328-5.

Abstract

To evaluate the importance of 11beta-hydroxysteroid dehydrogenase type 1 (11beta-HSD1) in insulin resistant diabetic C57BL/KsJ-db/db mice, we measured the activity and mRNA level of 11beta-HSD1 in the liver of db/db mice and their heterozygote litter mates, db/+m mice. The blood glucose, plasma insulin, and corticosterone levels of db/db mice were significantly higher than those of db/+m mice. Despite hyperinsulinemia, the activity level of this enzyme was significantly higher in db/db mice, and the mRNA level of hepatic 11beta-HSD1 was also significantly higher in db/db mice. Since hepatic 11beta-HSD1 in vivo mainly functions as 11-keto-reductase and does not work as 11beta-oxidase, these results suggest that the rate of hepatic conversion of 11-dehydrocorticosterone to corticosterone is increased in db/db mice, resulting in higher glucocorticoid activity in the liver. The increased hepatic corticosterone concentration due to the elevation of 11beta-HSD1 and high plasma corticosterone concentration may antagonize the action of insulin and cause insulin resistance. These findings have a potentially important implication for relationships between increased hepatic 11beta-HSD1 and insulin resistance in db/db mice. The present paper is the first to demonstrate the increased activities and mRNA level of hepatic 11beta-HSD1 in db/db mice.

摘要

为评估11β-羟类固醇脱氢酶1型(11β-HSD1)在胰岛素抵抗性糖尿病C57BL/KsJ-db/db小鼠中的重要性,我们检测了db/db小鼠及其杂合子同窝仔鼠(db/+m小鼠)肝脏中11β-HSD1的活性和mRNA水平。db/db小鼠的血糖、血浆胰岛素和皮质酮水平显著高于db/+m小鼠。尽管存在高胰岛素血症,但该酶的活性水平在db/db小鼠中显著更高,且肝脏11β-HSD1的mRNA水平在db/db小鼠中也显著更高。由于体内肝脏11β-HSD1主要作为11-酮还原酶起作用,而不作为11β-氧化酶起作用,这些结果表明在db/db小鼠中11-脱氢皮质酮向皮质酮的肝脏转化率增加,导致肝脏中糖皮质激素活性更高。由于11β-HSD1升高导致的肝脏皮质酮浓度增加以及高血浆皮质酮浓度可能拮抗胰岛素的作用并导致胰岛素抵抗。这些发现对于db/db小鼠中肝脏11β-HSD1增加与胰岛素抵抗之间的关系具有潜在重要意义。本文首次证明db/db小鼠肝脏中11β-HSD1的活性和mRNA水平增加。

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