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| Title: | Recent advances in renal tubular calcium reabsorption. |
| Author(s): | Mensenkamp, A.R. (229749526) Hoenderop, J.G.J. (195017544) Bindels, R.J.M. (07205378X) |
| Publication year: | 2006 |
| Document type: | Article / Letter to editor |
| Journal: | Current Opinion in Nephrology and Hypertension |
| ISSN: | 1062-4821 |
| Volume: | vol. 15 |
| Issue: | iss. 5 |
| Start page: | p. 524 |
| End page: | p. 529 |
| Abstract: | PURPOSE OF REVIEW: Knowledge of renal Ca2+ reabsorption has evolved greatly in recent years. This review focuses on two recent discoveries concerning passive and active Ca2+ reabsorption. RECENT FINDINGS: The thiazide diuretics are known for their hypocalciuric effect. Recently, it has been demonstrated that TRPV5-knockout mice, in which active Ca2+ reabsorption in the distal convoluted tubule is completely abolished, show the same sensitivity towards thiazides as wild-type mice. This indicates that thiazide affects Ca2+ reabsorption indirectly via contraction of the extracellular volume, independent of active Ca2+ reabsorption in the distal convoluted tubule, thereby increasing passive paracellular Ca2+ transport in the proximal tubule. Moreover, the antiaging hormone Klotho regulates Ca2+ reabsorption in the distal convoluted tubule via a novel molecular mechanism. Klotho stabilizes the TRPV5 Ca2+ channel in the plasma membrane by deglycosylation of the protein. SUMMARY: By showing that thiazide-induced hypercalciuria is due to increased passive Ca2+ reabsorption in the proximal tubule, a long-standing issue has been solved, underlining the importance of proximal paracellular Ca2+ reabsorption. Moreover, the molecular mechanism by which the antiaging hormone Klotho regulates TRPV5 activity may prove to be generally applicable in Klotho-mediated prevention of aging. |
| Subject: | UMCN 5.4: Renal disorders |
| Organization: | Physiology |
| Appears in Collections: | Academic bibliography
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Please use this identifier to cite or link to this item:
http://hdl.handle.net/2066/50497
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