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CHEMICAL STRUCTURE OF STEROIDS IN RELATION TO PROMOTION OF GROWTH OF THE VAGINA AND UTERUS OF THE HYPOPHYSECTOMIZED RAT
In the hypophysectomized albino rat which is protected from contact with steroids in the ration and environment the uterus and vagina are highly atrophic but are sensitive indicators of activity of substances which promote their growth. Both the pituitary growth hormone and certain steroids have the...
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
1954
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2136373/ https://www.ncbi.nlm.nih.gov/pubmed/13192249 |
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author | Huggins, Charles Jensen, Elwood V. Cleveland, Anne Stack |
author_facet | Huggins, Charles Jensen, Elwood V. Cleveland, Anne Stack |
author_sort | Huggins, Charles |
collection | PubMed |
description | In the hypophysectomized albino rat which is protected from contact with steroids in the ration and environment the uterus and vagina are highly atrophic but are sensitive indicators of activity of substances which promote their growth. Both the pituitary growth hormone and certain steroids have the common property of inducing growth of these tissues. The vaginal epithelium consists of 2 layers of cells which differ profoundly in their growth in response to steroids, depending on the molecular structure of these compounds. The differential response to modifications of chemical structures of steroids permits evaluation of the importance of the intramolecular components for the process of growth. The number and site of functional groups, the geometry of the molecule and the state of oxidation are of high importance in determining physiologic activity of steroids in the androstane series; these features are less specific in the estrane series. Side groups at positions C(3) and C(17) are of importance in the promotion of growth by steroids in the androstane series, but these active centers are not equivalent in their physiological influence. As a generalization, hydrogenation of the oxygen function at C(17) (but not at C(3)) and dehydrogenation at critical areas of the ring structure increase the quantitative efficacy of steroids in promoting growth. The position of double bonds and the state of oxidation at both C(3) and C(17) determine the qualitative type of growth—cellular pattern, which a compound in the androstane series induces in the vaginal epithelium. |
format | Text |
id | pubmed-2136373 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1954 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21363732008-04-17 CHEMICAL STRUCTURE OF STEROIDS IN RELATION TO PROMOTION OF GROWTH OF THE VAGINA AND UTERUS OF THE HYPOPHYSECTOMIZED RAT Huggins, Charles Jensen, Elwood V. Cleveland, Anne Stack J Exp Med Article In the hypophysectomized albino rat which is protected from contact with steroids in the ration and environment the uterus and vagina are highly atrophic but are sensitive indicators of activity of substances which promote their growth. Both the pituitary growth hormone and certain steroids have the common property of inducing growth of these tissues. The vaginal epithelium consists of 2 layers of cells which differ profoundly in their growth in response to steroids, depending on the molecular structure of these compounds. The differential response to modifications of chemical structures of steroids permits evaluation of the importance of the intramolecular components for the process of growth. The number and site of functional groups, the geometry of the molecule and the state of oxidation are of high importance in determining physiologic activity of steroids in the androstane series; these features are less specific in the estrane series. Side groups at positions C(3) and C(17) are of importance in the promotion of growth by steroids in the androstane series, but these active centers are not equivalent in their physiological influence. As a generalization, hydrogenation of the oxygen function at C(17) (but not at C(3)) and dehydrogenation at critical areas of the ring structure increase the quantitative efficacy of steroids in promoting growth. The position of double bonds and the state of oxidation at both C(3) and C(17) determine the qualitative type of growth—cellular pattern, which a compound in the androstane series induces in the vaginal epithelium. The Rockefeller University Press 1954-09-01 /pmc/articles/PMC2136373/ /pubmed/13192249 Text en Copyright © Copyright, 1954, by The Rockefeller Institute for Medical Research New York This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Article Huggins, Charles Jensen, Elwood V. Cleveland, Anne Stack CHEMICAL STRUCTURE OF STEROIDS IN RELATION TO PROMOTION OF GROWTH OF THE VAGINA AND UTERUS OF THE HYPOPHYSECTOMIZED RAT |
title | CHEMICAL STRUCTURE OF STEROIDS IN RELATION TO PROMOTION OF GROWTH OF THE VAGINA AND UTERUS OF THE HYPOPHYSECTOMIZED RAT |
title_full | CHEMICAL STRUCTURE OF STEROIDS IN RELATION TO PROMOTION OF GROWTH OF THE VAGINA AND UTERUS OF THE HYPOPHYSECTOMIZED RAT |
title_fullStr | CHEMICAL STRUCTURE OF STEROIDS IN RELATION TO PROMOTION OF GROWTH OF THE VAGINA AND UTERUS OF THE HYPOPHYSECTOMIZED RAT |
title_full_unstemmed | CHEMICAL STRUCTURE OF STEROIDS IN RELATION TO PROMOTION OF GROWTH OF THE VAGINA AND UTERUS OF THE HYPOPHYSECTOMIZED RAT |
title_short | CHEMICAL STRUCTURE OF STEROIDS IN RELATION TO PROMOTION OF GROWTH OF THE VAGINA AND UTERUS OF THE HYPOPHYSECTOMIZED RAT |
title_sort | chemical structure of steroids in relation to promotion of growth of the vagina and uterus of the hypophysectomized rat |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2136373/ https://www.ncbi.nlm.nih.gov/pubmed/13192249 |
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