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Free access | 10.1172/JCI109794

Cytochemical Bioassay of Parathyroid Hormone: CHARACTERISTICS OF THE ASSAY AND ANALYSIS OF CIRCULATING HORMONAL FORMS

David Goltzman, Brian Henderson, and Nigel Loveridge

Departments of Medicine, McGill University, Montreal, Canada H3A 2B2

Royal Victoria Hospital, Montreal, Canada H3A 2B2

Find articles by Goltzman, D. in: PubMed | Google Scholar

Departments of Medicine, McGill University, Montreal, Canada H3A 2B2

Royal Victoria Hospital, Montreal, Canada H3A 2B2

Find articles by Henderson, B. in: PubMed | Google Scholar

Departments of Medicine, McGill University, Montreal, Canada H3A 2B2

Royal Victoria Hospital, Montreal, Canada H3A 2B2

Find articles by Loveridge, N. in: PubMed | Google Scholar

Published June 1, 1980 - More info

Published in Volume 65, Issue 6 on June 1, 1980
J Clin Invest. 1980;65(6):1309–1317. https://doi.org/10.1172/JCI109794.
© 1980 The American Society for Clinical Investigation
Published June 1, 1980 - Version history
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Abstract

A cytochemical bioassay for parathyroid hormone (PTH) was used for the characterization of the biological activity of circulating forms of the hormone. PTH-stimulated glucose-6-phosphate dehydrogenase activity in distal convoluted tubule cells was quantitated by integrating microdensitometry and the response to native bovine (b)PTH(1-84) was found to be linear between graded doses of hormone from 5 fg/ml to 5 pg/ml. Synthetic bPTH(1-34) and human (h)PTH(1-34) elicited a parallel and equimolar response; however calcitonin, ACTH, glucagon, epinephrine, vasopressin, and insulin failed to significantly stimulate the enzyme in doses up to 100,000 times greater than the lowest concentration of bPTH used. The assay was capable of distinguishing hormonal activity in normal, hypoparathyroid, and hyperparathyroid human plasma. After gel chromatography, bioactivity in plasma of hyperparathyroid patients with skeletal disease but normal kidney function coeluted mainly with bPTH(1-84), whereas bioactivity in plasma of hyperparathyroid patients with skeletal disease but severe uremia coeluted in approximately equivalent amounts with bPTH(1-84) and hPTH(1-34). Despite the abundance of small molecular-weight bioactivity in the peripheral circulation in uremia, ∼85% of the bioactivity in the parathyroid venous effluent coeluted with bPTH(1-84). The results therefore demonstrate the sensitivity and specificity of the assay for PTH and its utility in measuring the hormone in human parathyroid disorders. The results furthermore demonstrate the importance of entities cochromatographing with bPTH(1-84) in comprising the circulating bioactive hormone in hyperparathyroidism, and support the concept of a biological role for smaller forms of PTH, at least in chronic renal failure.

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