PARATHYROID CELL-PROLIFERATION IN THE RAT - EFFECT OF AGE AND OF PHOSPHATE ADMINISTRATION AND RECOVERY

Citation
Q. Wang et al., PARATHYROID CELL-PROLIFERATION IN THE RAT - EFFECT OF AGE AND OF PHOSPHATE ADMINISTRATION AND RECOVERY, Endocrinology, 137(11), 1996, pp. 4558-4562
Citations number
38
Categorie Soggetti
Endocrynology & Metabolism
Journal title
ISSN journal
00137227
Volume
137
Issue
11
Year of publication
1996
Pages
4558 - 4562
Database
ISI
SICI code
0013-7227(1996)137:11<4558:PCITR->2.0.ZU;2-N
Abstract
Indirect evidence in human subjects and the low prevalence of mitotic figures in rats suggest that the adult parathyroid gland is a conditio nal renewal tissue with a low cell birth rate and long cell life span. Accordingly, in normal rats of different ages (8-22 weeks), we measur ed parathyroid cell and nuclear size, cell number, and gland volume by quantitative microscopy, and cell birth rate and cell life span by Ki -67 expression assuming a duration of expression of 24 h. We also exam ined the effects of phosphate administration and subsequent recovery. In normal rats, parathyroid volume, cell and nuclear profile area, and cell profile number did not change significantly between 8-22 weeks o f age. In younger rats, the calculated cell birth rate was 53.2%/yr, a nd mean cell life span was 1.9 yr, with a lower 95% confidence limit b ased on a logarithmic distribution of 6 months. Phosphate loading caus ed hyperphosphatemia, hypocalcemia, increased PTH secretion, and incre ased calcitriol production. There was an increase in parathyroid cell and nuclear size consistent with PTH hypersecretion per cell, but a la rger increase in cell number and gland volume due to a 3-fold increase in cell birth rate. Six weeks after withdrawal of phosphate administr ation, cell and nuclear size had fallen to normal, and cell birth rate to half-normal, but cell number and gland volume were even higher. No apoptosis was detected in any gland in any animal, probably because i t is short and infrequent, rather than absent altogether. The followin g conclusions were made. 1) In normal rats, parathyroid cell birth rat e is very low, but can be increased by hypocalcemia, establishing the status of the parathyroid gland as a conditional renewal tissue. 2) De spite subnormal cell birth rate, the hyperplasia induced by 8 weeks of phosphate administration could not regress to normal within the anima l's remaining life span.