Effects of Glucocorticoids on Fetal Rat Bone Collagen Synthesis in Vitro*

Endocrinology ◽  
1979 ◽  
Vol 104 (3) ◽  
pp. 715-721 ◽  
Author(s):  
JOHN W. DIETRICH ◽  
ERNESTO M. CANALIS ◽  
DONNA M. MAINA ◽  
LAWRENCE G. RAISZ
1975 ◽  
Vol 80 (4) ◽  
pp. 795-800 ◽  
Author(s):  
Norvald Langeland ◽  
Vigdis Teig

ABSTRACT Oestradiol-17β has been administered to hypophysectomized/castrated and to thyro-parathyroidectomized/castrated young mature female rats. Treatment with oestradiol-17β 5 μg/day per animal, was continued for 3 weeks. Bone pieces from tibia/femur metaphyses were incubated in vitro for 3 h in order to establish the bone collagen synthesis and resorption rates. The results were compared to results from a previous study on castrated female rats with intact hypophysis, thyroid and parathyroid glands. Bone from the thyro-parathyroidectomized/castrated rats treated with oestradiol-17β had a significantly reduced collagen resorption rate in vitro as compared to their paired controls. This is a result consistent with that of castrated female rats with intact thyroid and parathyroid glands treated with oestradiol. Oestradiol-17β had no detectable effect upon collagen metabolism in the hypophysectomized/castrated rats. It is concluded that the effect of oestradiol on bone resorption is not exerted via the parathyroid glands or parathyroid hormone. The possibility that oestrogens may act on bone via the hypophysis is discussed.


1985 ◽  
Vol 226 (3) ◽  
pp. 789-795 ◽  
Author(s):  
I Dickson ◽  
J Walls

The influence of an excess of retinol on bone formation was studied by using cultures of embryonic-chick calvaria. Retinol decreased collagen synthesis in a dose-dependent manner, non-collagenous protein synthesis being relatively unaffected. Collagen synthesis was significantly inhibited after 24 h of culture with retinol and was progressively decreased, compared with control cultures containing no retinol, as the period of culture was increased. The effect of retinol on collagen synthesis could be reversed by incubation of calvaria for further periods in retinol-free medium. Incorporation of [3H]thymidine and [3H]uridine into DNA and RNA respectively was not altered by culturing calvaria with retinol for 22 h. These latter findings, and the selectivity for collagen synthesis, all suggested that the effect observed was not a cell-toxicity phenomenon. The effect of retinol on collagen synthesis by chick calvarial osteoblasts was probably direct and not mediated by osteoclasts, since a negligible number of the latter cells is present in chick calvaria. In cultures of neonatal murine calvaria, which contain many osteoclasts, retinol similarly inhibited synthesis of collagen, but not of non-collagenous protein; the concentrations of retinol necessary to produce the response were similar to those required to stimulate bone resorption in vitro.


Endocrinology ◽  
1977 ◽  
Vol 100 (3) ◽  
pp. 668-674 ◽  
Author(s):  
ERNESTO M. CANALIS ◽  
JOHN W. DIETRICH ◽  
DONNA M. MAINA ◽  
LAWRENCE G. RAISZ

Metabolism ◽  
1977 ◽  
Vol 26 (10) ◽  
pp. 1079-1087 ◽  
Author(s):  
Ernesto M. Canalis ◽  
Raymond L. Hintz ◽  
John W. Dietrich ◽  
Donna M. Maina ◽  
Lawrence G. Raisz

1975 ◽  
Vol 80 (4) ◽  
pp. 775-783 ◽  
Author(s):  
Norvald Langeland

ABSTRACT The effect of oestradiol-17β treatment on bone collagen metabolism in vitro was studied in metaphyseal rat bone. Rats were oophorectomized and subsequently treated for 3 weeks with different doses of oestradiol-17β. Bone pieces were incubated in a modified Krebs-Ringer bicarbonate medium for 6 h. Synthesis of [14C] hydroxyproline from [14C]proline and the incorporation of this amino acid into the bone samples was determined and the collagen synthesis and accretion rates calculated from these data. Collagen resorption rates were calculated from measured release of non-radioactive hydroxyproline to the medium. Castration resulted in an increased rate of accretion and resorption of collagen. All doses of oestradiol tested in this study (1 to 20 μg per animal per day for 3 weeks) decreased both accretion and resorption rates to levels insignificantly different from those of the non-castrated control rats. Only the 2 μg treated group had significantly better collagen balance than the castrated untreated rats.


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