Literature DB >> 18004298

The effect of calcitriol, paricalcitol, and a calcimimetic on extraosseous calcifications in uremic rats.

I Lopez1, F J Mendoza, E Aguilera-Tejero, J Perez, F Guerrero, D Martin, M Rodriguez.   

Abstract

Vitamin D derivatives and calcimimetics are used to treat secondary hyperparathyroidism in patients with chronic renal failure. We investigated the effect of calcitriol, paricalcitol, and the calcimimetic AMG 641 on soft-tissue calcification in uremic rats with secondary hyperparathyroidism. Control and uremic rats were treated with vehicle, calcitriol, paricalcitol, AMG 641, or a combination of AMG 641 plus calcitriol or paricalcitol. Parathyroid hormone levels were reduced by all treatments but were better controlled by the combination of paricalcitol and AMG 641. The calcimimetic alone did not induce extraosseous calcification but co-administration of AMG 641 reduced soft-tissue calcification and aortic mineralization in both calcitriol- and paricalcitol-treated rats. Survival was significantly reduced in rats treated with calcitriol and this mortality was attenuated by co-treatment with AMG 641. Our study shows that extraskeletal calcification was present in animals treated with calcitriol and paricalcitol but not with AMG 641. When used in combination with paricalcitol, AMG 641 provided excellent control of secondary hyperparathyroidism and prevented mortality associated with the use of vitamin D derivatives without causing tissue calcification.

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Year:  2007        PMID: 18004298     DOI: 10.1038/sj.ki.5002675

Source DB:  PubMed          Journal:  Kidney Int        ISSN: 0085-2538            Impact factor:   10.612


  24 in total

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Review 2.  Mechanisms and treatment of extraosseous calcification in chronic kidney disease.

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Review 4.  Coronary artery calcification in chronic kidney disease: An update.

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Review 7.  Novel regulatory aspects of the extracellular Ca2+-sensing receptor, CaR.

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8.  The calcimimetic AMG 641 abrogates parathyroid hyperplasia, bone and vascular calcification abnormalities in uremic rats.

Authors:  Charles Henley; James Davis; Gerald Miller; Edward Shatzen; Russ Cattley; Xiaodong Li; David Martin; Wei Yao; Nancy Lane; Victoria Shalhoub
Journal:  Eur J Pharmacol       Date:  2009-05-24       Impact factor: 4.432

Review 9.  Phosphate: an old bone molecule but new cardiovascular risk factor.

Authors:  Navid Shobeiri; Michael A Adams; Rachel M Holden
Journal:  Br J Clin Pharmacol       Date:  2014-01       Impact factor: 4.335

10.  A Novel Model of Chronic Kidney Disease in Rats: Dietary Adenine in Combination with Unilateral Nephrectomy.

Authors:  Cristina Muñoz Abellán; Sandra Mangold-Gehring; Sina Micus; Gerald Beddies; Andreas Moritz; Elke Hartmann; Waldemar Lehmann; Frank Eitner
Journal:  Kidney Dis (Basel)       Date:  2019-01-16
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