Literature DB >> 5166965

Renal effects of calcitonin and parathyroid extract in man. Studies in hypoparathyroidism.

H G Haas, M A Dambacher, J Guncaga, T Lauffenbruger.   

Abstract

To clarify the controversial renal action of calcitonin (CT) and a possible interrelationship between CT and parathyroid hormone, eight patients with untreated surgical hypoparathyroidism were studied. Various calcitonins, i.e. extracted porcine, synthetic porcine, synthetic human, and synthetic salmon CT in doses of 150 Medical Research Council U or 1.5 mg were infused over a 3 hr period. Subsequently, six of the same subjects received 500 USP U parathyroid extract (PTE) (Eli Lilly & Co., Indianapolis, Ind.) in 3 hr and later a combination of CT and PTE. In addition, two patients were given an infusion of ammonium phosphate with the aim of producting a phosphaturia of comparable degree as seen after CT and PTE, thus differentiating hormonal from nonhormonal influences on cation excretion. A protocol of serial clearance (C) studies using the patients as their own controls was followed. Serum and urinary inorganic phosphate (P), calcium (Ca), magnesium (Mg), sodium (Na), potassium (K), and creatinine (Cr) were determined and the clearance values calculated. All CT peptides caused a uniform, immediate and significant increase of C(P), C(Na), C(K), C(Ca), and C(Mg), PTE evoked a rise of C(P), C(Na), and C(K), but C(Ca) and C(Mg) were reduced, the Ca and Na figures being not statistically significant. The administration of both CT and PTE resulted in a summation of individual hormone effects on Ca and Mg excretion. Phosphate infusion on the other hand induced an isolated phosphaturia but no concomitant changes of the urinary cations.The hypoparathyroid data demonstrate that calcitonin enhances urinary elimination of P, Na, K, Ca, and Mg independently of parathyroid action, CT and PTE act qualitatively similarly on P, Na, and K excretion, while an antagonism seems to exist for the renal handling of Ca and Mg.

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Year:  1971        PMID: 5166965      PMCID: PMC292219          DOI: 10.1172/JCI106770

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


  31 in total

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Journal:  Lancet       Date:  1968-04-27       Impact factor: 79.321

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Authors:  M Peacock; W G Robertson; B E Nordin
Journal:  Lancet       Date:  1969-02-22       Impact factor: 79.321

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Authors:  C Y Pak; B Ruskin; A Casper
Journal:  Endocrinology       Date:  1970-08       Impact factor: 4.736

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Authors:  J W Kennedy; F S Tanzer; R V Talmage
Journal:  Endocrinology       Date:  1969-10       Impact factor: 4.736

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  14 in total

1.  Superior local tolerability of human versus salmon calcitonin preparations in young healthy volunteers.

Authors:  C Wüster; W Schurr; S Scharla; F Raue; H W Minne; R Ziegler
Journal:  Eur J Clin Pharmacol       Date:  1991       Impact factor: 2.953

Review 2.  Engendering biased signalling from the calcium-sensing receptor for the pharmacotherapy of diverse disorders.

Authors:  K Leach; P M Sexton; A Christopoulos; A D Conigrave
Journal:  Br J Pharmacol       Date:  2014-03       Impact factor: 8.739

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Authors:  B Fåhraeus
Journal:  Urol Res       Date:  1974

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Journal:  J Endocrinol Invest       Date:  1981 Jan-Mar       Impact factor: 4.256

7.  Cloning, characterization, and expression of a human calcitonin receptor from an ovarian carcinoma cell line.

Authors:  A H Gorn; H Y Lin; M Yamin; P E Auron; M R Flannery; D R Tapp; C A Manning; H F Lodish; S M Krane; S R Goldring
Journal:  J Clin Invest       Date:  1992-11       Impact factor: 14.808

Review 8.  Proximal tubular NHEs: sodium, protons and calcium?

Authors:  R Todd Alexander; Henrik Dimke; Emmanuelle Cordat
Journal:  Am J Physiol Renal Physiol       Date:  2013-06-12

Review 9.  Pharmacology and therapeutic use of calcitonin.

Authors:  J C Stevenson; I M Evans
Journal:  Drugs       Date:  1981-04       Impact factor: 9.546

10.  Intracolonic bioavailability of human calcitonin in man.

Authors:  C Beglinger; W Born; R Muff; J Drewe; J L Dreyfuss; A Bock; M Mackay; J A Fischer
Journal:  Eur J Clin Pharmacol       Date:  1992       Impact factor: 2.953

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