Differential regulation of renal sodium-phosphate transporter by glucocorticoids during rat ontogeny

被引:14
作者
Guner, YS
Kiela, PR
Xu, H
Collins, JF
Ghishan, FK
机构
[1] Univ Arizona, Hlth Sci Ctr, Dept Pediat, Steele Mem Childrens Res Ctr, Tucson, AZ 85724 USA
[2] Univ Arizona, Hlth Sci Ctr, Dept Physiol, Steele Mem Childrens Res Ctr, Tucson, AZ 85724 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 1999年 / 277卷 / 05期
关键词
sodium-hydrogen exchanger isoform 3; RU-486; methylprednisolone; rat development; kidney;
D O I
10.1152/ajpcell.1999.277.5.C884
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The effects of chronic administration of methylprednisolone (MP) were studied on the ontogeny of the renal type II Na-P-i transporter (NaPi-2). Immunoblot analysis showed that MP did not alter the expression of NaPi-2 protein levels in suckling and weanling rats; however, there was an similar to 50% decrease in adolescent and adult rats. There was no change in Na-dependent P-i uptake in brush-border membrane vesicles in suckling rats, but there was an almost twofold decrease in adolescent rats induced by MP treatment. MP administration did not alter mRNA levels in suckling or adolescent rats. Dual injections with the glucocorticoid receptor blocker RU-486 (mifepristone) and MP did not reverse the downregulation of NaPi-2 immunoreactive protein levels in adolescent rats. To control for RU-486 antagonism efficiency, Na/H exchanger isoform 3 (NHES) protein levels were also assayed after injection with RU-486 and MP. As expected, NHE3 protein levels increased after MP injection; however, the increase was blocked in adolescent rats by RU-486. We conclude that there is an age-dependent responsiveness to glucocorticoids and that the marked decrease in NaPi-2 immunoreactive protein levels and activity in adolescent rats is due to posttranscriptional mechanisms.
引用
收藏
页码:C884 / C890
页数:7
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