Versatile steroid molecules at the end of the aldosterone pathway
18-hydroxycorticosterone converts spontaneously and reversibly to a variety of less polar forms and derivatives, some of which are precursors to aldosterone. In particular, 21-hydroxy-11β,18-oxido-4-pregnene-3,20-dione (18-DAL) is hydroxylated to aldosterone with high yields in the presence of malat...
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paper:paper_00224731_v27_n4-6_p791_Lantos2023-06-08T14:51:03Z Versatile steroid molecules at the end of the aldosterone pathway Aragones, Alcira Ceballos, Nora Raquel Burton, Gerardo Cozza, Eduardo Néstor aldosterone hormone precursor reduced nicotinamide adenine dinucleotide phosphate cattle metabolism mitochondrion nonhuman short survey 18-Hydroxycorticosterone Acid-Base Equilibrium Adrenal Cortex Aldosterone Animal Chemistry Homeostasis Hydrogen-Ion Concentration Protein Precursors Steroids 18-hydroxycorticosterone converts spontaneously and reversibly to a variety of less polar forms and derivatives, some of which are precursors to aldosterone. In particular, 21-hydroxy-11β,18-oxido-4-pregnene-3,20-dione (18-DAL) is hydroxylated to aldosterone with high yields in the presence of malate and NADP+ at pH 4.8.18-DAL also behaves as a metabolic intermediate between 18-OH-B and aldosterone accorcling to time-course and trapping experiments. Consequently, the final steps of the aldosterone pathway at pH 4.8 could be identified as 18-OH-B,18-DAL and aldosterone, in this sequence. The submitochondrial distribution of aldosterone biosynthesis is compatible with this postulate. The work also shows that some forms of 18-OH-B are promoters of hydrogen transport in renal tubuli and that this regulation may be independent of sodium reabsorption. These results suggest a regulatory model, new in steroid biology, accorcling to which steroid molecules bearing an oxidized angular C18-methyl may undergo structural changes between precursor ("P") and hormonal ("H") forms in response to homeostatic requirements. © 1987. Fil:Aragonés, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Ceballos, N.R. 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. Fil:Cozza, E.N. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 1987 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00224731_v27_n4-6_p791_Lantos http://hdl.handle.net/20.500.12110/paper_00224731_v27_n4-6_p791_Lantos |
institution |
Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-134 |
collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
topic |
aldosterone hormone precursor reduced nicotinamide adenine dinucleotide phosphate cattle metabolism mitochondrion nonhuman short survey 18-Hydroxycorticosterone Acid-Base Equilibrium Adrenal Cortex Aldosterone Animal Chemistry Homeostasis Hydrogen-Ion Concentration Protein Precursors Steroids |
spellingShingle |
aldosterone hormone precursor reduced nicotinamide adenine dinucleotide phosphate cattle metabolism mitochondrion nonhuman short survey 18-Hydroxycorticosterone Acid-Base Equilibrium Adrenal Cortex Aldosterone Animal Chemistry Homeostasis Hydrogen-Ion Concentration Protein Precursors Steroids Aragones, Alcira Ceballos, Nora Raquel Burton, Gerardo Cozza, Eduardo Néstor Versatile steroid molecules at the end of the aldosterone pathway |
topic_facet |
aldosterone hormone precursor reduced nicotinamide adenine dinucleotide phosphate cattle metabolism mitochondrion nonhuman short survey 18-Hydroxycorticosterone Acid-Base Equilibrium Adrenal Cortex Aldosterone Animal Chemistry Homeostasis Hydrogen-Ion Concentration Protein Precursors Steroids |
description |
18-hydroxycorticosterone converts spontaneously and reversibly to a variety of less polar forms and derivatives, some of which are precursors to aldosterone. In particular, 21-hydroxy-11β,18-oxido-4-pregnene-3,20-dione (18-DAL) is hydroxylated to aldosterone with high yields in the presence of malate and NADP+ at pH 4.8.18-DAL also behaves as a metabolic intermediate between 18-OH-B and aldosterone accorcling to time-course and trapping experiments. Consequently, the final steps of the aldosterone pathway at pH 4.8 could be identified as 18-OH-B,18-DAL and aldosterone, in this sequence. The submitochondrial distribution of aldosterone biosynthesis is compatible with this postulate. The work also shows that some forms of 18-OH-B are promoters of hydrogen transport in renal tubuli and that this regulation may be independent of sodium reabsorption. These results suggest a regulatory model, new in steroid biology, accorcling to which steroid molecules bearing an oxidized angular C18-methyl may undergo structural changes between precursor ("P") and hormonal ("H") forms in response to homeostatic requirements. © 1987. |
author |
Aragones, Alcira Ceballos, Nora Raquel Burton, Gerardo Cozza, Eduardo Néstor |
author_facet |
Aragones, Alcira Ceballos, Nora Raquel Burton, Gerardo Cozza, Eduardo Néstor |
author_sort |
Aragones, Alcira |
title |
Versatile steroid molecules at the end of the aldosterone pathway |
title_short |
Versatile steroid molecules at the end of the aldosterone pathway |
title_full |
Versatile steroid molecules at the end of the aldosterone pathway |
title_fullStr |
Versatile steroid molecules at the end of the aldosterone pathway |
title_full_unstemmed |
Versatile steroid molecules at the end of the aldosterone pathway |
title_sort |
versatile steroid molecules at the end of the aldosterone pathway |
publishDate |
1987 |
url |
https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00224731_v27_n4-6_p791_Lantos http://hdl.handle.net/20.500.12110/paper_00224731_v27_n4-6_p791_Lantos |
work_keys_str_mv |
AT aragonesalcira versatilesteroidmoleculesattheendofthealdosteronepathway AT ceballosnoraraquel versatilesteroidmoleculesattheendofthealdosteronepathway AT burtongerardo versatilesteroidmoleculesattheendofthealdosteronepathway AT cozzaeduardonestor versatilesteroidmoleculesattheendofthealdosteronepathway |
_version_ |
1768541551983591424 |