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This Article Full Text Full Text (PDF) All Versions of this Article: 287/6/F1164    most recent 00437.2003v1 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 ISI 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 ISI Web of Science (13) Citing Articles via Google Scholar Google Scholar Articles by Lee, C.-T. Articles by Lien, Y.-H. H. Search for Related Content PubMed PubMed Citation Articles by Lee, C.-T. Articles by Lien, Y.-H. H.

Effect of thiazide on renal gene expression of apical calcium channels and calbindins

¹Division of Nephrology, Department of Medicine, Chang-Gung Memorial Hospital, and ²Graduate Institute of Medicine, Kaohsiung Medical University, Kaohsiung 833, Taiwan; and ³Department of Medicine, University of Arizona, Tucson, Arizona 85724

Submitted 11 December 2003 ; accepted in final form 13 July 2004

Thiazide diuretics are specific inhibitors of the Na-Cl cotransporter in the distal convoluted tubule (DCT). In addition to producing diuresis and natriuresis, they have a hypocalciuric effect. Recently, two apical calcium channels have been identified, transient receptor potential vanilloid 5 (TRPV5) and TRPV6; both are expressed in the DCT. We studied the effects of thiazides on mouse renal calcium handling and renal gene expression of TRPV5 and TRPV6, as well as calbindin-D_28k and calbindin-D_9k, both of which are calcium transport facilitators located in the DCT. Upregulation of renal TRPV5 was found 4 h after intraperitoneal injection of chlorothiazide (CTZ) at both 25 and 50 mg/kg, but not at 100 mg/kg. Chronic treatment with CTZ at 25 mg/kg twice daily for 3 days, with or without salt supplementation of 0.8% NaCl and 0.1% KCl in the drinking water, caused hypocalciuria, but the gene expression patterns were different. Without salt supplementation, mice developed volume contraction and there were no changes in gene expression. When volume contraction was prevented by salt supplementation, there was a significant increase in gene expression of TRPV5, calbindin-D_28k, and calbindin-D_9k. Salt supplementation alone also induced significant upregulation of TRPV5, TRPV6, and both calbindins. The upregulation of TRPV5 by CTZ and salt supplementation and salt alone was further confirmed with immunofluorescent staining studies. Our studies suggest that thiazides induce hypocalciuria through different mechanisms depending on volume status. With volume contraction, increased calcium reabsorption in the proximal tubule plays the major role. Without volume contraction, hypocalciuria is probably achieved through increased calcium reabsorption in the DCT by the activation of a transcellular calcium transport system and upregulation of apical calcium channel TRPV5, calbindin-D_28k, and calbindin-D_9k.

chlorothiazide; transient receptor potential vanilloid 5; transient receptor potential vanilloid 6; calbindin-D_28k; calbindin-D_9k

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