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1 Department of Medicine, Winthrop-University Hospital, Mineola, New York 11501; and 2 The Health Sciences Center, State University of New York at Stony Brook, Stony Brook, New York 11794
To investigate whether growth hormone (GH) and
17
-estradiol (E2) replacement
can prevent osteopenia induced by pituitary and ovarian hormone
deficiency [by hypophysectomy and ovariectomy (HX+OV)], we
administered relatively low doses of GH (2.3 IU · kg
1 · day
1)
and E2 (100 µg · kg
1 · wk
1)
in experiment
1 and relatively high doses of GH
(13.5 IU · kg
1 · day
1)
and E2 (3,500 µg · kg
1 · wk
1)
in experiment
2 to 2-mo-old HX+OV Sprague-Dawley
rats for 6 wk. Our data show that the HX+OV of rats results in
diminished periosteal bone formation, longitudinal bone growth, and
decreased cancellous bone volume. Administration of either the low or
high dose of GH to these rats increased their systemic growth, serum levels of osteocalcin, and cortical bone formation. Either low or high
doses of GH or E2 alone only
partially prevent cancellous bone loss. However, the combined treatment
of GH plus E2 resulted in an
additive increase in the cancellous bone mass. We conclude that the
additive effect of GH plus E2 on
cancellous bone is attributed to the suppressive effect of
E2 on bone resorption and the
anabolic effect of GH on bone formation.
osteoporosis; bone formation; histomorphometry; insulin-like growth factor I; cancellous bone
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