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Research Article Free access | 10.1172/JCI105624
Department of Medicine and the Clinical Research Center, Marquette University School of Medicine and Milwaukee County General Hospital, Milwaukee, Wis.
†Address requests for reprints to Dr. Jacob Lemann, Jr., Dept. of Medicine, Marquette University School of Medicine, Milwaukee County General Hospital, 8700 West Wisconsin Ave., Milwaukee, Wis. 53226.
*Submitted for publication January 5, 1967; accepted April 20, 1967.
This investigation was supported in part by U. S. Public Health Service research grant 5 M01 FR-00058 and in part by U. S. Public Health Service research grant 2 R01 AM-08924.
Find articles by Lemann, J. in: JCI | PubMed | Google Scholar
Department of Medicine and the Clinical Research Center, Marquette University School of Medicine and Milwaukee County General Hospital, Milwaukee, Wis.
†Address requests for reprints to Dr. Jacob Lemann, Jr., Dept. of Medicine, Marquette University School of Medicine, Milwaukee County General Hospital, 8700 West Wisconsin Ave., Milwaukee, Wis. 53226.
*Submitted for publication January 5, 1967; accepted April 20, 1967.
This investigation was supported in part by U. S. Public Health Service research grant 5 M01 FR-00058 and in part by U. S. Public Health Service research grant 2 R01 AM-08924.
Find articles by Litzow, J. in: JCI | PubMed | Google Scholar
Department of Medicine and the Clinical Research Center, Marquette University School of Medicine and Milwaukee County General Hospital, Milwaukee, Wis.
†Address requests for reprints to Dr. Jacob Lemann, Jr., Dept. of Medicine, Marquette University School of Medicine, Milwaukee County General Hospital, 8700 West Wisconsin Ave., Milwaukee, Wis. 53226.
*Submitted for publication January 5, 1967; accepted April 20, 1967.
This investigation was supported in part by U. S. Public Health Service research grant 5 M01 FR-00058 and in part by U. S. Public Health Service research grant 2 R01 AM-08924.
Find articles by Lennon, E. in: JCI | PubMed | Google Scholar
Published August 1, 1967 - More info
We carried out clearance studies in nine healthy adults and four patients with hypoparathyroidism before and after inducing stable metabolic acidosis with either NH4Cl or acetazolamide. Clearances were repeated in seven normal subjects and three of the patients 3 days after stopping these agents.
During acidosis in the normal subjects, serum ultrafilterable calcium concentration rose significantly, but inulin clearance fell to a greater extent, so that the calculated filtered load of calcium fell significantly. Despite this, urinary calcium excretion rose. Urinary calcium excretion remained elevated in the recovery studies when the serum ultrafilterable calcium concentration and filtered load of calcium had returned to control levels. Evidence is presented indicating that the increased calcium excretion which occurred during acidosis and recovery clearances was not due to natriuresis or to increased excretion of complexing anions. The comparable results in the four patients with hypoparathyroidism, two of whom also had hypothyroidism, suggest that the capacity to alter secretion rates of parathyroid hormone, thyrocalcitonin or both is not a critical determinant of the augmented rates of calcium excretion during acidosis.
We conclude that metabolic acidosis produces increased urinary calcium excretion by causing decreased renal tubular calcium reabsorption. Evidence is presented which suggests that this is a direct effect of metabolic acidosis on metabolic processes within renal tubular cells.