Glucocorticoids and IIβ-hydroxysteroid dehydrogenase type 2 gene expression in the aging kidney

被引:13
作者
Audigé, A
Dick, B
Frey, BM
Frey, FJ
Corman, B
Vogt, B
机构
[1] Univ Bern, Inselspital, Div Nephrol & Hypertens, CH-3010 Bern, Switzerland
[2] Serv Biol Cellulaire, Gif Sur Yvette, France
关键词
11; beta-HSD; aging; gene expression; glucocorticoids; progesterone;
D O I
10.1046/j.1365-2362.2002.01003.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Aging is associated with increased concentrations of circulating glucocorticoids, a situation expected to induce a glucocorticoid-mediated mineralocorticoid effect, resulting in sodium retention and hypertension unless counteracting mechanisms are operative. Conversion of glucocorticoids to inert 11beta-keto compounds by the enzyme I 11beta-hydroxysteroid dehydrogenase type 2 (11beta-HSD2) is one of these mechanisms. We hypothesized therefore that 11beta-HSD2 gene expression and/or activity increase with age in male WAG/Rij rats, a strain without increased blood pressure with age or senescence-related obesity or kidney disease. Materials and methods Corticosterone (B) concentrations in plasma and urinary excretion of corticosterone and dehydrocorticosterone (A) tetrahydro metabolites, THB + 5alpha-THB + THA, were assessed by gas chromatography-mass spectrometry (GC-MS) in 10-month-old-rats (n = 6) and in 30-month-old rats (n = 6). Renal 11beta-HSD2 messenger ribonucleic acid (mRNA) abundance was measured by real-time quantitative TaqMan polymerase chain reaction and microarray assays. Results Thirty-month-old rats had significantly higher corticosterone concentrations in plasma and increased urinary excretion of corticosterone and dehydrocorticosterone tetrahydro metabolites. Conversion of B to A in kidney microsomes from 30-month-old rats was moderately but not significantly increased compared with 10-month-old rats. The urinary ratios of (THB + 5alpha-THB)/THA and free B/A and renal 11beta-HSD2 mRNA abundance were equal in 10- and 30-month-old rats. Conclusions There is no evidence for an enhanced gene expression or activity of renal 11beta-HSD2 in these aging rats, suggesting either that endogenous 11beta-HSD2 is able to cope with the increased corticosterone concentrations characteristic of the aging process or that alternative mechanisms contribute to the maintenance of a normal sodium excretion in these animals.
引用
收藏
页码:411 / 420
页数:10
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