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Am J Physiol Endocrinol Metab 286: E780-E785, 2004. First published January 13, 2004; doi:10.1152/ajpendo.00473.2003
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Role of acidosis-induced increases in calcium on PTH secretion in acute metabolic and respiratory acidosis in the dog

Ignacio López,1 Escolástico Aguilera-Tejero,1 José Carlos Estepa,1 Mariano Rodríguez,2 and Arnold J. Felsenfeld3

1Departamento de Medicina y Cirugía Animal, Universidad de Córdoba, 14014 Cordoba; 2Departamento de Nefrología y Unidad de Investigación, Hospital Universitario Reina Sofia, 14004 Cordoba, Spain; and 3Department of Medicine, West Los Angeles Veterans Affairs Medical Center and the University of California at Los Angeles, Los Angeles 90024, California

Submitted 20 October 2003 ; accepted in final form 5 January 2004

Recently, we showed that both acute metabolic acidosis and respiratory acidosis stimulate parathyroid hormone (PTH) secretion in the dog. To evaluate the specific effect of acidosis, ionized calcium (iCa) was clamped at a normal value. Because iCa values normally increase during acute acidosis, we now have studied the PTH response to acute metabolic and respiratory acidosis in dogs in which the iCa concentration was allowed to increase (nonclamped) compared with dogs with a normal iCa concentration (clamped). Five groups of dogs were studied: control, metabolic (clamped and nonclamped), and respiratory (clamped and nonclamped) acidosis. Metabolic (HCl infusion) and respiratory (hypoventilation) acidosis was progressively induced during 60 min. In the two clamped groups, iCa was maintained at a normal value with an EDTA infusion. Both metabolic and respiratory acidosis increased (P < 0.05) iCa values in nonclamped groups. In metabolic acidosis, the increase in iCa was progressive and greater (P < 0.05) than in respiratory acidosis, in which iCa increased by 0.04 mM and then remained constant despite further pH reductions. The increase in PTH values was greater (P < 0.05) in clamped than in nonclamped groups (metabolic and respiratory acidosis). In the nonclamped metabolic acidosis group, PTH values first increased and then decreased from peak values when iCa increased by >0.1 mM. In the nonclamped respiratory acidosis group, PTH values exceeded (P < 0.05) baseline values only after iCa values stopped increasing at a pH of 7.30. For the same increase in iCa in the nonclamped groups, PTH values increased more in metabolic acidosis. In conclusion, 1) both metabolic acidosis and respiratory acidosis stimulate PTH secretion; 2) the physiological increase in the iCa concentration during the induction of metabolic and respiratory acidosis reduces the magnitude of the PTH increase; 3) in metabolic acidosis, the increase in the iCa concentration can be of sufficient magnitude to reverse the increase in PTH values; and 4) for the same degree of acidosis-induced hypercalcemia, the increase in PTH values is greater in metabolic than in respiratory acidosis.

hypercalcemia; metabolic acidosis; parathyroid hormone; respiratory acidosis



Address for reprint requests and other correspondence: E. Aguilera-Tejero, Dept. Medicina y Cirugía Animal, Campus Universitario Rabanales, Ctra Madrid-Cádiz km 396, 14014 Córdoba, Spain (E-mail: pv1agtee{at}uco.es).




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