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1 Laboratorio de
Fisiología,
The liver of adult
mammals contains various classes of polyploid hepatocytes produced by a
process that is partially regulated by hormones. However, it is not
well understood how the hormones affect the rate of hepatocyte
proliferation under physiological conditions. Here we have studied the
specific roles of 3,5,3'-triiodothyronine (T3), growth hormone (GH), and
sex steroids on the percentage of diploid nuclei in S phase and on the
population of liver tetraploid (4C) cell nuclei in several rat model
systems. Gonadal steroids had no effect on the S phase but account for
gender differences in the 4C nuclei. Hypophysectomy in adult male rats
produced a moderate decrease in 4C nuclei that was reversed by
treatment with 25 µg
T3 · kg
1 · day
1,
whereas treatment with 200 µg human recombinant GH
(hGH) · kg
1 · day
1
was ineffective. Rats made hypothyroid by methimazole treatment of dams
and pups until death showed a low S phase and only 5% of 4C nuclei at
70 days of age. T3 significantly
increased the S phase 24 h after administration and restored the adult
normal level of 4C nuclei after 10 days of treatment. hGH did not
affect the 4C nuclei or the S phase in the hypothyroid rats. These
results suggest that the processes of hepatocyte proliferation and
polyploidization of the rat liver are under endocrine control, with
thyroid hormones playing the essential regulatory role.
liver polyploidy; flow cytometry; cell cycle
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