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Corticosteroid Induction of Renal and Intestinal K(+)-dependent P-nitrophenylphosphatase in Young and Adult Rats

Overview
Journal Histochem J
Specialty Biochemistry
Date 1996 Sep 1
PMID 8910033
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Abstract

The post-natal development of the K(+)-dependent p-nitrophenylphosphatase (K-NPPase) activity of the Na, K-ATPase complex and its regulation by corticosteroids was studied in renal and intestinal epithelia of the rat using the p-nitrophenylphosphatecerium capture method. The distribution of the phosphatase was analysed in detail in the renal epithelia of the medullary thick ascending limb of Henle's loop and distal convoluted tubule and in the surface epithelial cells of the distal colon. The convoluted tubule and Henle's loop segments showed a stronger reaction for K-NPPase than the colon epithelium both in adult and young animals (suckling and weanling pups). The intensity of staining rose progressively in all three epithelia during early postnatal development and reached the highest levels during the weaning period and in adulthood. The most distinct change was observed between days 10 and 16. Adrenalectomy significantly reduced the density of the final reaction product in weanling and adult rats. Replacement hormone therapy of adrenalectomized weanling rats with the glucocorticoid dexamethasone restored the K-NPPase activity in the two renal epithelia, whereas the mineralocorticoid deoxycorticosterone acetate had no effect on the activity in the medullary thick ascending limb, a very slight effect in distal convoluted tubules, and a strong effect on the distal colon epithelial activity. The observed small effect of the mineralocorticoid in distal convoluted tubule activity may reflect a cross-over into glucocorticoid receptors. We conclude that the postnatal development of Na, K-ATPase is regulated by glucocorticoids in nephron epithelia and predominantly by mineralocorticoids in the surface enterocytes of the distal colon.

References
1.
Henning S . Plasma concentrations of total and free corticosterone during development in the rat. Am J Physiol. 1978; 235(5):E451-6. DOI: 10.1152/ajpendo.1978.235.5.E451. View

2.
Halbhuber K, Gossrau R, Moller U, Hulstaert C, Zimmermann N, FEUERSTEIN H . The cerium perhydroxide-diaminobenzidine (Ce-H2O2-DAB) procedure. New methods for light microscopic phosphatase histochemistry and immunohistochemistry. Histochemistry. 1988; 90(4):289-97. DOI: 10.1007/BF00495973. View

3.
Farman N, Vandewalle A, Bonvalet J . Autoradiographic determination of dexamethasone binding sites along the rabbit nephron. Am J Physiol. 1983; 244(3):F325-34. DOI: 10.1152/ajprenal.1983.244.3.F325. View

4.
Firth J, Marland B . The significance of inhibitor-resistant alkaline phosphatase in the cytochemical demonstration of transport adenosine triphosphatase. J Histochem Cytochem. 1975; 23(8):571-4. DOI: 10.1177/23.8.169303. View

5.
Doucet A . Function and control of Na-K-ATPase in single nephron segments of the mammalian kidney. Kidney Int. 1988; 34(6):749-60. DOI: 10.1038/ki.1988.245. View