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spelling todo:paper_00137227_v108_n5_p1697_Heller2023-10-03T14:11:06Z Binding of [3H]dexamethasone by rat placenta Heller, C. Coirini, H. De Nicola, A.F. dexamethasone glucocorticoid receptor mercaptoethanol n ethylmaleimide steroid receptor tritium corticosterone dexamethasone drug receptor estradiol hormone receptor n ethylmaleimide progesterone promegestone radioisotope testosterone animal article binding competition cell nucleus cytosol female kinetics metabolism placenta pregnancy rat animal experiment corticosterone h 3 dexamethasone h 3 endocrine system female genital system placenta pregnancy promegestone h 3 Animal Binding, Competitive Cell Nucleus Cytosol Dexamethasone Ethylmaleimide Female Kinetics Mercaptoethanol Placenta Pregnancy Rats Receptors, Glucocorticoid Receptors, Steroid Support, Non-U.S. Gov't Tritium [3H]Dexamethasone binding was measured in the basal zone trophoblast (BZT) and the labyrinthine zone (LZ) of placenta from Wistar rats on days 19–22 of pregnancy. Cytosol from both zones was incubated with [3H]dexamethasone for 4 h at 0–4 C, and high affinity, low capacity sites were measured by Scatchard plot analysis in BZT and LZ, tissues which demonstrated similar concentrations of sites and affinity constants. Specific binding was decreased by omitting mercaptoethanol from the incubation buffer, by adding N-ethylmaleimide, or by increasing the temperature to 16 or 37 C. Competition studies revealed that the rank order of inhibition of [3H]dexamethasone binding by nonradioactive steroids was dexamethasone ≫ progesterone = corticosterone ≫ testosterone = 17α-estradiol. Dexamethasone-binding sites could be distinguished from progestinbinding sites by competition analysis as well as by the absence of 17α, 21-dimethyl-19-nor-pregna-4, 9-diene-3, 20-dione ([3H]-R5020) binding in LZ, whereas the corticoid was bound to both zones. Nuclei from BZT and LZ took up radioactive steroid when exposed to cytosol prelabeled with [3H]dexamethasone, but little radioactivity was present in nuclei incubated with buffer containing [3H]dexamethasone. After in vivo administration of [3H]dexamethasone to pregnant rats, radioactivity was recovered in nuclei and cytosol from both placental zones. Furthermore, whole homogenates or cytosol from BZT or LZ did not metabolize [3H]dexamethasone to any significant extent. These results suggest that rat placenta contains dexamethasonebinding sites which resemble the glucocorticoid receptors described in other tissues. © 1981 by The Endocrine Society. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00137227_v108_n5_p1697_Heller
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic dexamethasone
glucocorticoid receptor
mercaptoethanol
n ethylmaleimide
steroid receptor
tritium
corticosterone
dexamethasone
drug receptor
estradiol
hormone receptor
n ethylmaleimide
progesterone
promegestone
radioisotope
testosterone
animal
article
binding competition
cell nucleus
cytosol
female
kinetics
metabolism
placenta
pregnancy
rat
animal experiment
corticosterone h 3
dexamethasone h 3
endocrine system
female genital system
placenta
pregnancy
promegestone h 3
Animal
Binding, Competitive
Cell Nucleus
Cytosol
Dexamethasone
Ethylmaleimide
Female
Kinetics
Mercaptoethanol
Placenta
Pregnancy
Rats
Receptors, Glucocorticoid
Receptors, Steroid
Support, Non-U.S. Gov't
Tritium
spellingShingle dexamethasone
glucocorticoid receptor
mercaptoethanol
n ethylmaleimide
steroid receptor
tritium
corticosterone
dexamethasone
drug receptor
estradiol
hormone receptor
n ethylmaleimide
progesterone
promegestone
radioisotope
testosterone
animal
article
binding competition
cell nucleus
cytosol
female
kinetics
metabolism
placenta
pregnancy
rat
animal experiment
corticosterone h 3
dexamethasone h 3
endocrine system
female genital system
placenta
pregnancy
promegestone h 3
Animal
Binding, Competitive
Cell Nucleus
Cytosol
Dexamethasone
Ethylmaleimide
Female
Kinetics
Mercaptoethanol
Placenta
Pregnancy
Rats
Receptors, Glucocorticoid
Receptors, Steroid
Support, Non-U.S. Gov't
Tritium
Heller, C.
Coirini, H.
De Nicola, A.F.
Binding of [3H]dexamethasone by rat placenta
topic_facet dexamethasone
glucocorticoid receptor
mercaptoethanol
n ethylmaleimide
steroid receptor
tritium
corticosterone
dexamethasone
drug receptor
estradiol
hormone receptor
n ethylmaleimide
progesterone
promegestone
radioisotope
testosterone
animal
article
binding competition
cell nucleus
cytosol
female
kinetics
metabolism
placenta
pregnancy
rat
animal experiment
corticosterone h 3
dexamethasone h 3
endocrine system
female genital system
placenta
pregnancy
promegestone h 3
Animal
Binding, Competitive
Cell Nucleus
Cytosol
Dexamethasone
Ethylmaleimide
Female
Kinetics
Mercaptoethanol
Placenta
Pregnancy
Rats
Receptors, Glucocorticoid
Receptors, Steroid
Support, Non-U.S. Gov't
Tritium
description [3H]Dexamethasone binding was measured in the basal zone trophoblast (BZT) and the labyrinthine zone (LZ) of placenta from Wistar rats on days 19–22 of pregnancy. Cytosol from both zones was incubated with [3H]dexamethasone for 4 h at 0–4 C, and high affinity, low capacity sites were measured by Scatchard plot analysis in BZT and LZ, tissues which demonstrated similar concentrations of sites and affinity constants. Specific binding was decreased by omitting mercaptoethanol from the incubation buffer, by adding N-ethylmaleimide, or by increasing the temperature to 16 or 37 C. Competition studies revealed that the rank order of inhibition of [3H]dexamethasone binding by nonradioactive steroids was dexamethasone ≫ progesterone = corticosterone ≫ testosterone = 17α-estradiol. Dexamethasone-binding sites could be distinguished from progestinbinding sites by competition analysis as well as by the absence of 17α, 21-dimethyl-19-nor-pregna-4, 9-diene-3, 20-dione ([3H]-R5020) binding in LZ, whereas the corticoid was bound to both zones. Nuclei from BZT and LZ took up radioactive steroid when exposed to cytosol prelabeled with [3H]dexamethasone, but little radioactivity was present in nuclei incubated with buffer containing [3H]dexamethasone. After in vivo administration of [3H]dexamethasone to pregnant rats, radioactivity was recovered in nuclei and cytosol from both placental zones. Furthermore, whole homogenates or cytosol from BZT or LZ did not metabolize [3H]dexamethasone to any significant extent. These results suggest that rat placenta contains dexamethasonebinding sites which resemble the glucocorticoid receptors described in other tissues. © 1981 by The Endocrine Society.
format JOUR
author Heller, C.
Coirini, H.
De Nicola, A.F.
author_facet Heller, C.
Coirini, H.
De Nicola, A.F.
author_sort Heller, C.
title Binding of [3H]dexamethasone by rat placenta
title_short Binding of [3H]dexamethasone by rat placenta
title_full Binding of [3H]dexamethasone by rat placenta
title_fullStr Binding of [3H]dexamethasone by rat placenta
title_full_unstemmed Binding of [3H]dexamethasone by rat placenta
title_sort binding of [3h]dexamethasone by rat placenta
url http://hdl.handle.net/20.500.12110/paper_00137227_v108_n5_p1697_Heller
work_keys_str_mv AT hellerc bindingof3hdexamethasonebyratplacenta
AT coirinih bindingof3hdexamethasonebyratplacenta
AT denicolaaf bindingof3hdexamethasonebyratplacenta
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