Features of the shuttle pair 11β-hydroxyprogesterone-11- ketoprogesterone

11β-hydroxyprogesterone (HOP) and 11-ketoprogesterone (KP) are reversible components of a shuttle pair whose interconversion in rat liver is catalyzed by isoform-1 of 11β-hydroxysteroid dehydrogenase. Kidneys also produce this interconversion. The present study was carried out to investigate the shu...

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Autores principales: Vicent, Guillermo Pablo, Burton, Gerardo
Publicado: 1997
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rat
Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0039128X_v62_n4_p358_Galigniana
http://hdl.handle.net/20.500.12110/paper_0039128X_v62_n4_p358_Galigniana
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spelling paper:paper_0039128X_v62_n4_p358_Galigniana2023-06-08T15:03:17Z Features of the shuttle pair 11β-hydroxyprogesterone-11- ketoprogesterone Vicent, Guillermo Pablo Burton, Gerardo 11β-hydroxyprogesterone 11β-hydroxysteroid dehydrogenase 11-ketoprogesterone shuttle pair sodium retention 11beta hydroxyprogesterone 11beta hydroxysteroid dehydrogenase 3 [(3 cholamidopropyl)dimethylammonio] 1 propanesulfonic acid corticosterone dehydrocorticosterone mineralocorticoid receptor animal cell animal experiment animal model animal tissue article enzyme activity male nonhuman oxidation ph rat receptor binding shuttle vector sodium retention tissue specificity 11-beta-Hydroxysteroid Dehydrogenases Adrenalectomy Animals Binding, Competitive Cholic Acids Enzyme Induction Hydrogen-Ion Concentration Hydroxyprogesterones Hydroxysteroid Dehydrogenases Male Progesterone Rats Rats, Sprague-Dawley Receptors, Glucocorticoid Receptors, Mineralocorticoid Sodium Transcortin Tyrosine Transaminase Animalia Humulus 11β-hydroxyprogesterone (HOP) and 11-ketoprogesterone (KP) are reversible components of a shuttle pair whose interconversion in rat liver is catalyzed by isoform-1 of 11β-hydroxysteroid dehydrogenase. Kidneys also produce this interconversion. The present study was carried out to investigate the shuttle pair and its components in the rat. As in corticosterone/11 -dehydrocorticosterone, oxidation is more effective at an alkaline pH, while reduction prevails at a neutral pH. Moreover, both reactions are inhibited by the detergent 3-[(3-cholamido propyl)- dimethylammonio]-1-propane-sulphonate (CHAPS). However, at variance with the 11-ketosteroids cortisone (E) and 11-dehydrocorticosterone (A) thought to be 'inactive,' KP has slight direct Na+-retaining properties, and it, as well as HOP, induces glucocorticoids (11β-hydroxycorticoids) to retain sodium. 11-ketoprogesterone exhibits 17 times better affinity for native type I mineralocorticoid receptor than HOP and a 3-fold affinity for partially purified (transcortin free) mineralocorticoid receptor. However, KP, in contrast to HOP, binds only weakly to transcortin, not at all to glucocorticoid receptor, and requires reduction at C11 for tyrosine aminotransferase (TAT) induction. Fil:Vicent, G.P. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Burton, G. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 1997 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0039128X_v62_n4_p358_Galigniana http://hdl.handle.net/20.500.12110/paper_0039128X_v62_n4_p358_Galigniana
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic 11β-hydroxyprogesterone
11β-hydroxysteroid dehydrogenase
11-ketoprogesterone
shuttle pair
sodium retention
11beta hydroxyprogesterone
11beta hydroxysteroid dehydrogenase
3 [(3 cholamidopropyl)dimethylammonio] 1 propanesulfonic acid
corticosterone
dehydrocorticosterone
mineralocorticoid receptor
animal cell
animal experiment
animal model
animal tissue
article
enzyme activity
male
nonhuman
oxidation
ph
rat
receptor binding
shuttle vector
sodium retention
tissue specificity
11-beta-Hydroxysteroid Dehydrogenases
Adrenalectomy
Animals
Binding, Competitive
Cholic Acids
Enzyme Induction
Hydrogen-Ion Concentration
Hydroxyprogesterones
Hydroxysteroid Dehydrogenases
Male
Progesterone
Rats
Rats, Sprague-Dawley
Receptors, Glucocorticoid
Receptors, Mineralocorticoid
Sodium
Transcortin
Tyrosine Transaminase
Animalia
Humulus
spellingShingle 11β-hydroxyprogesterone
11β-hydroxysteroid dehydrogenase
11-ketoprogesterone
shuttle pair
sodium retention
11beta hydroxyprogesterone
11beta hydroxysteroid dehydrogenase
3 [(3 cholamidopropyl)dimethylammonio] 1 propanesulfonic acid
corticosterone
dehydrocorticosterone
mineralocorticoid receptor
animal cell
animal experiment
animal model
animal tissue
article
enzyme activity
male
nonhuman
oxidation
ph
rat
receptor binding
shuttle vector
sodium retention
tissue specificity
11-beta-Hydroxysteroid Dehydrogenases
Adrenalectomy
Animals
Binding, Competitive
Cholic Acids
Enzyme Induction
Hydrogen-Ion Concentration
Hydroxyprogesterones
Hydroxysteroid Dehydrogenases
Male
Progesterone
Rats
Rats, Sprague-Dawley
Receptors, Glucocorticoid
Receptors, Mineralocorticoid
Sodium
Transcortin
Tyrosine Transaminase
Animalia
Humulus
Vicent, Guillermo Pablo
Burton, Gerardo
Features of the shuttle pair 11β-hydroxyprogesterone-11- ketoprogesterone
topic_facet 11β-hydroxyprogesterone
11β-hydroxysteroid dehydrogenase
11-ketoprogesterone
shuttle pair
sodium retention
11beta hydroxyprogesterone
11beta hydroxysteroid dehydrogenase
3 [(3 cholamidopropyl)dimethylammonio] 1 propanesulfonic acid
corticosterone
dehydrocorticosterone
mineralocorticoid receptor
animal cell
animal experiment
animal model
animal tissue
article
enzyme activity
male
nonhuman
oxidation
ph
rat
receptor binding
shuttle vector
sodium retention
tissue specificity
11-beta-Hydroxysteroid Dehydrogenases
Adrenalectomy
Animals
Binding, Competitive
Cholic Acids
Enzyme Induction
Hydrogen-Ion Concentration
Hydroxyprogesterones
Hydroxysteroid Dehydrogenases
Male
Progesterone
Rats
Rats, Sprague-Dawley
Receptors, Glucocorticoid
Receptors, Mineralocorticoid
Sodium
Transcortin
Tyrosine Transaminase
Animalia
Humulus
description 11β-hydroxyprogesterone (HOP) and 11-ketoprogesterone (KP) are reversible components of a shuttle pair whose interconversion in rat liver is catalyzed by isoform-1 of 11β-hydroxysteroid dehydrogenase. Kidneys also produce this interconversion. The present study was carried out to investigate the shuttle pair and its components in the rat. As in corticosterone/11 -dehydrocorticosterone, oxidation is more effective at an alkaline pH, while reduction prevails at a neutral pH. Moreover, both reactions are inhibited by the detergent 3-[(3-cholamido propyl)- dimethylammonio]-1-propane-sulphonate (CHAPS). However, at variance with the 11-ketosteroids cortisone (E) and 11-dehydrocorticosterone (A) thought to be 'inactive,' KP has slight direct Na+-retaining properties, and it, as well as HOP, induces glucocorticoids (11β-hydroxycorticoids) to retain sodium. 11-ketoprogesterone exhibits 17 times better affinity for native type I mineralocorticoid receptor than HOP and a 3-fold affinity for partially purified (transcortin free) mineralocorticoid receptor. However, KP, in contrast to HOP, binds only weakly to transcortin, not at all to glucocorticoid receptor, and requires reduction at C11 for tyrosine aminotransferase (TAT) induction.
author Vicent, Guillermo Pablo
Burton, Gerardo
author_facet Vicent, Guillermo Pablo
Burton, Gerardo
author_sort Vicent, Guillermo Pablo
title Features of the shuttle pair 11β-hydroxyprogesterone-11- ketoprogesterone
title_short Features of the shuttle pair 11β-hydroxyprogesterone-11- ketoprogesterone
title_full Features of the shuttle pair 11β-hydroxyprogesterone-11- ketoprogesterone
title_fullStr Features of the shuttle pair 11β-hydroxyprogesterone-11- ketoprogesterone
title_full_unstemmed Features of the shuttle pair 11β-hydroxyprogesterone-11- ketoprogesterone
title_sort features of the shuttle pair 11β-hydroxyprogesterone-11- ketoprogesterone
publishDate 1997
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0039128X_v62_n4_p358_Galigniana
http://hdl.handle.net/20.500.12110/paper_0039128X_v62_n4_p358_Galigniana
work_keys_str_mv AT vicentguillermopablo featuresoftheshuttlepair11bhydroxyprogesterone11ketoprogesterone
AT burtongerardo featuresoftheshuttlepair11bhydroxyprogesterone11ketoprogesterone
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