COLONIC SODIUM-POTASSIUM ADENOSINE-TRIPHOSPHATE SUBUNIT GENE-EXPRESSION - ONTOGENY AND REGULATION BY ADRENOCORTICAL STEROIDS

被引:86
作者
FULLER, PJ
VERITY, K
机构
[1] Medical Research Centre, Prince Henry’s Hospital, Melbourne
[2] Medical Research Centre, Prince Henry’s Hospital, Melbourne, 3004, St. Kilda Road
关键词
D O I
10.1210/endo-127-1-32
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mineralocorticoids and glucocorticoids exhibit overlapping but distinct effects on transepithelial sodium transport in the descending colon. Na.K-ATPase, the major sodium pump, has been variously reported to be regulated by one or both classes of steroids. The present studies explore the ontogeny and steroidal regulation of Na.K-ATPase α- and β-subunit mRNA levels in the descending colon. In descending colon, subunit mRNA levels are low before birth, increasing to reach adult levels at approximately day 25. Dexamethasone treatment caused a rapid dose-dependent increase in colonic Na.K-ATPase subunit mRNA levels. The specific glucocorticoid RU26988 also increased subunit mRNA levels. Aldosterone administration, at doses adequate to yield a profound antinatriuresis, did not alter subunit mRNA levels. Carbenoloxone sodium produced an approximately 3-fold increase in subunit mRNA levels in intact but not adrenalecto- mized rats. We have demonstrated that Na.K-ATPase subunit gene expression is: 1) low in the fetal colon but achieves plateau levels by day 25; 2) acutely regulated by corticosteroids via type II rather than type I receptors; and 3) increased by carbenoxolone sodium, presumably as a result of increased occupancy of the type II receptor by corticosterone. © 1990 by The Endocrine Society.
引用
收藏
页码:32 / 38
页数:7
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