Literature DB >> 1133175

The acute effect of chlorothiazide on serum-ionized calcium. Evidence for a parathyroid hormone-dependent mechanism.

M M Popovtzer, V L Subryan, A C Alfrey, E B Reeve, R W Schrier.   

Abstract

The acute effects of chlorothiazide (CTZ) on total (TSCA) and ionized (SCA-plus 2) serum calcium concentrations were studied in three groups of people: (a) eight subjects with normal parathyroid function; (b) six patients with hypoparathyroidism; and (c) two patients with hyperparathyroidism. Most subjects were studied on four occasions; at least 3 days intervened between studies on an individual subject. During each experiment the subject received an i.v. influsion of 5% dextrose in water at 1 ml/min from 8 a.m. to 4 p.m. Additions to the infusions were (a) none; (b) CTZ to deliver 3.33 mg/kg/h; (c) parathyroid extract to deliver 1 U/kg/h; or (d) both CTZ and parathyroid extract at the rates previously indicated. CTZ, when used, was added to the infusion at 10 a.m., parathyroid extract at 8 a.m. When CTZ was infused, the diuretic-induced losses of Na and water were replaced by i.v. infusion. In normal subjects 2 h after the start of CTZ infusion, there was a transient increase in SCA-plus 2 which coincided in time of day with a transient decrease in SCA-plus 2 in control experiments. At that time of day SCA-plus 2 was 4.18 plus or minus 0.12 mg/100 ml in control experiments and 4.56 plus or minus 0.08 in experiments with CTZ, P smaller than 0.025. The corresponding values for (TSCA) were 9.32 plus or minus 0.15 and 9.80 plus or minus 0.30, P smaller than 0.01. Such differences were not observed in the group with hypoparathyroidism. In the two patients with hyperparathyroidism, CTZ produced sustained increases in TSCA and SCA-plus 2. In normal subjects and those with hypoparathyroidism, CTZ plus parathyroid extract infusion resulted in sustained increases in both SCA-plus 2 and TSCA throughout the periods of observation when compared to experiments in which only parathyroid extract was infused, P smaller than 0.01 in all instances. The results suggest that the acute hypercalcemic action of CTZ requires the presence of circulating parathyroid hormone.

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Year:  1975        PMID: 1133175      PMCID: PMC301885          DOI: 10.1172/JCI108049

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  21 in total

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Journal:  Clin Chem       Date:  1965-04       Impact factor: 8.327

2.  The effect of parathyroid extract on renal tubular calcium reabsorption in the dog.

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Journal:  J Clin Invest       Date:  1962-12       Impact factor: 14.808

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Authors:  A LICHTWITZ; R PARLIER; D HIOCO; L MIRAVET
Journal:  Sem Med Prof Med Soc       Date:  1961 Aug 14-20

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Authors:  B A LAMBERG; B KUHLBACK
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Journal:  J Clin Invest       Date:  1972-04       Impact factor: 14.808

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  3 in total

Review 1.  The pathophysiology and clinical aspects of hypercalcemic disorders.

Authors:  D B Lee; E T Zawada; C R Kleeman
Journal:  West J Med       Date:  1978-10

2.  The modulatory effect of endogenous parathyroid hormone on the action of hydrochlorothiazide in pseudohypoparathyroidism type I.

Authors:  K Mizunashi; Y Furukawa; K Abe; K Yoshinaga
Journal:  Calcif Tissue Int       Date:  1994-06       Impact factor: 4.333

3.  The calcium-sensing receptor (CaSR) defends against hypercalcemia independently of its regulation of parathyroid hormone secretion.

Authors:  Lakshmi Kantham; Steven J Quinn; Ogo I Egbuna; Khanjan Baxi; Robert Butters; Jian L Pang; Martin R Pollak; David Goltzman; Edward M Brown
Journal:  Am J Physiol Endocrinol Metab       Date:  2009-10       Impact factor: 4.310

  3 in total

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