Abstract
With the development of radioligand binding assays for identifying hormone receptors directly, it has become evident that the number of receptors in a particular cell or tissue does not remain constant but can in fact, be regulated by a variety of agents1. Receptor concentrations decrease with exposure to homologous hormone (called densitization or down-regulation) but may be affected differently by heterologous hormones. Thus in the adrenergic contractile response of rabbit myometrium, mediated by α-adrenergic receptors2, the concentration of α-adrenergic receptors is regulated by sex steroids3,4. This oestrogen treatment increases the concentration of myometrial α-adrenergic receptors approximately threefold over that measured in myometrium from immature rabbits, and, furthermore, is accompanied by an increased contractile response to catecholamines5. We report here that, after 24 h in organ culture. rabbit myometrium is more sensitive to α-adrenergic stimulation in vitro, and that particulate fractions prepared from cultured myometrium have a threefold increase in αadrenergic receptors but not β-adrenergic receptors when compared with myometrium that has not been cultured. Our results suggest that the myometrium α-adrenergic receptor, in addition to being regulated by oestrogen, seems to be under tonic inhibitory control in vivo and that this control may only in part be accounted for by catecholamines.
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Cornett, L., Goldfien, A. & Roberts, J. Tonic in vivo inhibition of rabbit myometrial adrenergic receptors. Nature 292, 623–625 (1981). https://doi.org/10.1038/292623a0
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DOI: https://doi.org/10.1038/292623a0
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