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猪肠道不同区域11β-羟基类固醇脱氢酶2的活性

Activities of 11beta-hydroxysteroid dehydrogenase 2 in different regions of the intestinal tract of pigs.

作者信息

Claus R, Raab S, Lacorn M

机构信息

FG Tierhaltung und Leistungsphysiologie, Institut für Tierhaltung und Tierzüchtung, Universität Hohenheim, Garbenstrasse 17, D-70599 Stuttgart, Germany.

出版信息

Exp Clin Endocrinol Diabetes. 2001;109(7):374-7. doi: 10.1055/s-2001-17410.

Abstract

11beta-Hydroxysteroid dehydrogenase 2 (11beta-HSD 2) converts active cortisol to inactive cortisone and thus modifies the availability of glucocorticoids for the target tissue. An additional function is the protection of the aldosterone receptor in mineralocorticoid-sensitive tissues such as the kidney and the gut. The occurrence of 11beta-HSD 2 activity was investigated in several species. Data for the pig, however, so far are missing. The activity was determined by a radio-enzyme-assay based on the conversion of tritiated cortisol to cortisone under standardized incubation conditions in supernatants of homogenates prepared from tissues of four castrates. Tissues comprised several locations along the intestinal tract and in addition kidney, lung, muscle, heart, spleen and pancreas. Highest values of the enzyme activity were found in kidney and very low activities in lung tissue but no activity in muscle, spleen, heart and pancreas. In the gut, there was a continuous increase in enzyme activity from the duodenum (0.60 pmol x min(- 1) x mg protein(- 1)) towards the colon with maximum values in the colon transversum (23.32 pmol x min(- 1) x mg protein(- 1)). In the colon the activity was 10-fold higher than in jejunum and 3-fold higher compared to ileum. The activities did not differ significantly between the colon transversum and colon descendens.

摘要

11β-羟类固醇脱氢酶2(11β-HSD 2)可将活性皮质醇转化为无活性的可的松,从而改变糖皮质激素对靶组织的可利用性。其另一功能是保护盐皮质激素敏感组织(如肾脏和肠道)中的醛固酮受体。已对多个物种的11β-HSD 2活性进行了研究。然而,目前尚无猪的相关数据。该活性通过放射性酶法测定,该方法基于在标准化孵育条件下,将从四只去势动物组织匀浆上清液中的氚化皮质醇转化为可的松。组织包括沿肠道的多个部位,以及肾脏、肺、肌肉、心脏、脾脏和胰腺。酶活性最高值出现在肾脏,肺组织中的活性非常低,而肌肉、脾脏、心脏和胰腺中无活性。在肠道中,从十二指肠(0.60 pmol·min⁻¹·mg蛋白⁻¹)到结肠,酶活性持续增加,横结肠中达到最高值(23.32 pmol·min⁻¹·mg蛋白⁻¹)。结肠中的活性比空肠高10倍,比回肠高3倍。横结肠和降结肠之间的活性无显著差异。

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