Abstract
ABSTRACT
The uterus as well as slices from the diaphragm of immature mice were incubated in vitro with tritium-labelled oestrogens. The active oestrogens, 17β-oestradiol and meso-hexoestrol, were preferentially accumulated by the uterus. The racemic isomer of hexoestrol which is less oestrogenic than the meso-isomer was not preferentially accumulated by the uterus. The addition of non-radioactive 17α- or 17β-oestradiol, meso- or racemic hexoestrol inhibited the uptake of 17β-oestradiol-3H by the uterus but not by the diaphragm. The most oestrogenic isomer found was the one most effective in inhibiting uptake. Prior injection of 17β-oestradiol in vivo inhibited the uptake in vitro of 17β-oestradiol-3H. It is concluded that the uptake of oestrogens by the mouse uterus in vitro is stereospecific in the same way as the uptake in vivo.
Subject
Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism
Cited by
37 articles.
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