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Research Article Free access | 10.1172/JCI110052
Endocrine Unit, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts 02114
Harvard Medical School, Boston, Massachusetts 02114
Find articles by Segre, G. in: JCI | PubMed | Google Scholar
Endocrine Unit, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts 02114
Harvard Medical School, Boston, Massachusetts 02114
Find articles by D'Amour, P. in: JCI | PubMed | Google Scholar
Endocrine Unit, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts 02114
Harvard Medical School, Boston, Massachusetts 02114
Find articles by Hultman, A. in: JCI | PubMed | Google Scholar
Endocrine Unit, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts 02114
Harvard Medical School, Boston, Massachusetts 02114
Find articles by Potts, J. in: JCI | PubMed | Google Scholar
Published February 1, 1981 - More info
Reports from several laboratories, showing extensive hepatic extraction of circulating parathyroid hormone, led us to examine the effect of near-total hepatectomy on the metabolism of the hormone to circulating fragments, and on its clearance from plasma. The rate of disappearance of 125I-labeled and unlabeled bovine parathyroid hormone from plasma, and the appearance, disappearance, and chemical and immunochemical characteristics of circulating fragments were examined by gel filtration and either sequence-specific radioimmunoassays or sequence analysis using the Edman reaction. Results from awake rats subjected to near-total hepatectomy were compared with those found in sham-treated, nephrectomized, and short-term uremic rats (studied 2 d after nephrectomy). When compared with the sham-treated group, all other groups clear 125I-labeled hormone more slowly; after hepatectomy, however, the clearance rate is most strikingly decreased.
After injection of intact hormone, the concentration of carboxy-terminal fragments in the circulation of hepatectomized rats is greatly reduced at all time intervals when compared with that in sham-treated rats. Sequence analysis of plasma samples, collected from rats into which 125I-labeled hormone had been injected, shows that carboxy-terminal fragments having positions 34 and 37 of the intact hormone sequence as their amino-terminal amino acids are abundant in sham-treated, nephrectomized, and nephrectomized/uremic rats, but are undetectable in hepatectomized rats. The data suggest that inasmuch as the liver in vivo generates most of the carboxy-terminal fragments resulting from the metabolism of injected hormone, specific cell types within the liver must be the principal locus of the responsible enzyme(s); thus, studies of the enzymic properties of isolated hepatic cells in vitro most likely will yield information of physiologic relevance to the metabolism of the hormone in the intact animal.