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Control of pulsatile and tonic parathyroid hormone secretion by ionized calcium.
J Clin Endocrinol Metab. 1996 Dec; 81(12):4236-43.JC

Abstract

To investigate the effect of changes in ionized calcium on instantaneous PTH secretion, we examined seven young healthy volunteers by 1-min blood sampling under conditions of normo-, hypo-, and hypercalcemia. After a baseline period of 75 min, ambient ionized calcium was either increased or decreased by 0.2 mmol/L for 105 min by clamped infusion of calcium gluconate or sodium citrate. The characteristics of PTH secretion were analyzed by a deconvolution technique, accounting for subject-specific plasma PTH disappearance half-life, as measured during the first 15 min of calcium infusion (range, 2.04-2.93 min). The process regularity of pulsatile PTH secretion was evaluated by an approximate entropy statistic. Under baseline conditions, 32% of total PTH secretion was released in a pulsatile fashion, with a burst frequency of 6.9 +/- 0.8 h-1 and a PTH mass per burst of 2.6 +/- 0.9 pmol/L. The remaining 68% of total secretion was attributed to tonic hormone release. During the initial 30 min of induced hypocalcemia, pulsatile secretion increased by 1140%, whereas tonic secretion did not change. The preferential increase in pulsatile PTH secretion was mediated by a combined rise in burst frequency and mass released per burst. During subsequent steady state hypocalcemia, the tonic secretion rate increased (255% of baseline), whereas burst frequency and burst mass decreased (to 103% and 189% of the baseline values), restoring the baseline ratio of tonic to pulsatile PTH secretion. The regularity of PTH release increased during steady state hypocalcemia. During hypercalcemia, tonic secretion, burst mass, and burst frequency decreased by 75%, 82%, and 32%, respectively, and remained constant throughout the clamp period. We conclude that acute hypocalcemia elicits an immediate pulsatile and a delayed tonic secretory response of the parathyroid gland with increased regularity of PTH release. Acute hypercalcemia suppresses both the pulsatile and the tonic component of PTH secretion.

Authors+Show Affiliations

Department of Pediatrics, University of Heidelberg, Germany.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, Non-P.H.S.
Research Support, U.S. Gov't, P.H.S.

Language

eng

PubMed ID

8954021

Citation

Schmitt, C P., et al. "Control of Pulsatile and Tonic Parathyroid Hormone Secretion By Ionized Calcium." The Journal of Clinical Endocrinology and Metabolism, vol. 81, no. 12, 1996, pp. 4236-43.
Schmitt CP, Schaefer F, Bruch A, et al. Control of pulsatile and tonic parathyroid hormone secretion by ionized calcium. J Clin Endocrinol Metab. 1996;81(12):4236-43.
Schmitt, C. P., Schaefer, F., Bruch, A., Veldhuis, J. D., Schmidt-Gayk, H., Stein, G., Ritz, E., & Mehls, O. (1996). Control of pulsatile and tonic parathyroid hormone secretion by ionized calcium. The Journal of Clinical Endocrinology and Metabolism, 81(12), 4236-43.
Schmitt CP, et al. Control of Pulsatile and Tonic Parathyroid Hormone Secretion By Ionized Calcium. J Clin Endocrinol Metab. 1996;81(12):4236-43. PubMed PMID: 8954021.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Control of pulsatile and tonic parathyroid hormone secretion by ionized calcium. AU - Schmitt,C P, AU - Schaefer,F, AU - Bruch,A, AU - Veldhuis,J D, AU - Schmidt-Gayk,H, AU - Stein,G, AU - Ritz,E, AU - Mehls,O, PY - 1996/12/1/pubmed PY - 1996/12/1/medline PY - 1996/12/1/entrez SP - 4236 EP - 43 JF - The Journal of clinical endocrinology and metabolism JO - J. Clin. Endocrinol. Metab. VL - 81 IS - 12 N2 - To investigate the effect of changes in ionized calcium on instantaneous PTH secretion, we examined seven young healthy volunteers by 1-min blood sampling under conditions of normo-, hypo-, and hypercalcemia. After a baseline period of 75 min, ambient ionized calcium was either increased or decreased by 0.2 mmol/L for 105 min by clamped infusion of calcium gluconate or sodium citrate. The characteristics of PTH secretion were analyzed by a deconvolution technique, accounting for subject-specific plasma PTH disappearance half-life, as measured during the first 15 min of calcium infusion (range, 2.04-2.93 min). The process regularity of pulsatile PTH secretion was evaluated by an approximate entropy statistic. Under baseline conditions, 32% of total PTH secretion was released in a pulsatile fashion, with a burst frequency of 6.9 +/- 0.8 h-1 and a PTH mass per burst of 2.6 +/- 0.9 pmol/L. The remaining 68% of total secretion was attributed to tonic hormone release. During the initial 30 min of induced hypocalcemia, pulsatile secretion increased by 1140%, whereas tonic secretion did not change. The preferential increase in pulsatile PTH secretion was mediated by a combined rise in burst frequency and mass released per burst. During subsequent steady state hypocalcemia, the tonic secretion rate increased (255% of baseline), whereas burst frequency and burst mass decreased (to 103% and 189% of the baseline values), restoring the baseline ratio of tonic to pulsatile PTH secretion. The regularity of PTH release increased during steady state hypocalcemia. During hypercalcemia, tonic secretion, burst mass, and burst frequency decreased by 75%, 82%, and 32%, respectively, and remained constant throughout the clamp period. We conclude that acute hypocalcemia elicits an immediate pulsatile and a delayed tonic secretory response of the parathyroid gland with increased regularity of PTH release. Acute hypercalcemia suppresses both the pulsatile and the tonic component of PTH secretion. SN - 0021-972X UR - https://www.unboundmedicine.com/medline/citation/8954021/Control_of_pulsatile_and_tonic_parathyroid_hormone_secretion_by_ionized_calcium_ L2 - https://academic.oup.com/jcem/article-lookup/doi/10.1210/jcem.81.12.8954021 DB - PRIME DP - Unbound Medicine ER -