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This Article Full Text Full Text (PDF) All Versions of this Article: 293/1/F186    most recent 00484.2006v1 Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in Web of Science Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via Web of Science (8) Citing Articles via Google Scholar Google Scholar Articles by Usa, K. Articles by Liang, M. Search for Related Content PubMed PubMed Citation Articles by Usa, K. Articles by Liang, M.

Renal interstitial corticosterone and 11-dehydrocorticosterone in conscious rats

¹Department of Physiology, Medical College of Wisconsin, Milwaukee; ²Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota; ³Department of Medicine, Medical College of Wisconsin, Milwaukee; and ⁴Endocrine Research Laboratory, Aurora St. Luke's Medical Center, Milwaukee, Wisconsin

Submitted 7 December 2006 ; accepted in final form 23 March 2007

Deficiencies in the conversion between active and inactive glucocorticoids in the kidney can lead to hypertension. However, the significance of glucocorticoid metabolism in specific kidney regions in vivo is not clear, possibly in part due to the difficulty in measuring glucocorticoid levels in kidney regions in vivo. We used microdialysis techniques to sample renal interstitial fluid from conscious rats. The levels of corticosterone (active) and 11-dehydrocorticosterone (inactive) were analyzed by liquid chromatography-tandem mass spectrometry. Direct infusion of the 11-hydroxysteroid dehydrogenase (11-HSD) inhibitor carbenoxolone into the renal medulla induced hypertension, and significantly increased corticosterone levels and the corticosterone/11-dehydrocorticosterone ratio, an index of 11-HSD activity, in the renal medullary microdialysate, but not in urine or the plasma. Further characterization of conscious, untreated rats (n = 13–16) indicated that corticosterone concentrations (ng/ml) were 0.8 ± 0.1, 1.0 ± 0.1, 66.7 ± 8.1, and 7.9 ± 1.1 in cortical microdialysate, medullary microdialysate, the plasma, and urine, respectively. The corticosterone/11-dehydrocorticosterone ratios were 0.8 ± 0.1, 0.6 ± 0.1, 10.6 ± 1.4, and 1.7 ± 0.1, respectively, in these 4 types of sample. The expression level of 11-HSD1 was higher in the medulla than in the cortex, whereas 11-HSD2 was most enriched in the outer medulla. Microdialysate levels of corticosterone were 1.6-fold higher in afternoons than in mornings, whereas plasma levels differed by 2.8-fold. These results demonstrated that corticosterone excess in the renal medulla might be sufficient to cause hypertension and provided the first characterization of renal interstitial glucocorticoids.

hypertension; 11-hydroxysteroid dehydrogenase; microdialysis; mass spectrometry

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