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THE EFFECT OF HYDROCORTISONE ON THE RESPONSE OF FETAL RAT SKIN IN CULTURE TO ULTRAVIOLET IRRADIATION
1. The effect of hydrocortisone on the development of fetal rat skin in organ culture, and on its repair after exposure to a mixed beam from a mercury lamp, are described. 2. The addition of hydrocortisone (7.5 µg/ml) to the culture medium (HC medium) caused accelerated differentiation and keratinis...
Autores principales: | , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
1962
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2137545/ https://www.ncbi.nlm.nih.gov/pubmed/14005935 |
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author | Weissmann, Gerald Fell, Honor B. |
author_facet | Weissmann, Gerald Fell, Honor B. |
author_sort | Weissmann, Gerald |
collection | PubMed |
description | 1. The effect of hydrocortisone on the development of fetal rat skin in organ culture, and on its repair after exposure to a mixed beam from a mercury lamp, are described. 2. The addition of hydrocortisone (7.5 µg/ml) to the culture medium (HC medium) caused accelerated differentiation and keratinisation of the epidermis followed by atrophic changes as in vivo. 3. Explants were grown for 2 days in either normal or HC medium and then irradiated with light from an Hanovia lamp. 4. Irradiation of the control explants produced severe necrosis in both epidermis and dermis and much disorganisation of the dermal intercellular material; 2 days after exposure the s. corneum with adherent cellular debris had become either completely detached from the denuded dermis, or raised to form a fluid-filled blister. Epidermal regeneration had begun by the 4th day after irradiation and was usually complete by the 6th day. 5. Hydrocortisone modified the response to irradiation as follows: (1) reduced and retarded cellular breakdown, (2) prevented vesication, (3) preserved the organisation of the dermal intercellular material, (4) hastened epithelialisation, (5) accelerated the differentiation of the new epidermis. Effects (2), (3), and (4) were probably secondary to (1). 6. Experiments with various light filters showed that the effective wavelengths for producing lesions in the skin explants were those below 3000 A. 7. It is suggested that the beneficial effect of hydrocortisone on the repair of irradiated skin explants might be due, at least in part, to a reduced proteolytic activity in the damaged tissue through a stabilising action of the hormone on the lysosomes. 8. The relationship of these findings to clinical observations is discussed. |
format | Text |
id | pubmed-2137545 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1962 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21375452008-04-17 THE EFFECT OF HYDROCORTISONE ON THE RESPONSE OF FETAL RAT SKIN IN CULTURE TO ULTRAVIOLET IRRADIATION Weissmann, Gerald Fell, Honor B. J Exp Med Article 1. The effect of hydrocortisone on the development of fetal rat skin in organ culture, and on its repair after exposure to a mixed beam from a mercury lamp, are described. 2. The addition of hydrocortisone (7.5 µg/ml) to the culture medium (HC medium) caused accelerated differentiation and keratinisation of the epidermis followed by atrophic changes as in vivo. 3. Explants were grown for 2 days in either normal or HC medium and then irradiated with light from an Hanovia lamp. 4. Irradiation of the control explants produced severe necrosis in both epidermis and dermis and much disorganisation of the dermal intercellular material; 2 days after exposure the s. corneum with adherent cellular debris had become either completely detached from the denuded dermis, or raised to form a fluid-filled blister. Epidermal regeneration had begun by the 4th day after irradiation and was usually complete by the 6th day. 5. Hydrocortisone modified the response to irradiation as follows: (1) reduced and retarded cellular breakdown, (2) prevented vesication, (3) preserved the organisation of the dermal intercellular material, (4) hastened epithelialisation, (5) accelerated the differentiation of the new epidermis. Effects (2), (3), and (4) were probably secondary to (1). 6. Experiments with various light filters showed that the effective wavelengths for producing lesions in the skin explants were those below 3000 A. 7. It is suggested that the beneficial effect of hydrocortisone on the repair of irradiated skin explants might be due, at least in part, to a reduced proteolytic activity in the damaged tissue through a stabilising action of the hormone on the lysosomes. 8. The relationship of these findings to clinical observations is discussed. The Rockefeller University Press 1962-09-01 /pmc/articles/PMC2137545/ /pubmed/14005935 Text en Copyright © Copyright, 1962, by The Rockefeller Institute 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 Weissmann, Gerald Fell, Honor B. THE EFFECT OF HYDROCORTISONE ON THE RESPONSE OF FETAL RAT SKIN IN CULTURE TO ULTRAVIOLET IRRADIATION |
title | THE EFFECT OF HYDROCORTISONE ON THE RESPONSE OF FETAL RAT SKIN IN CULTURE TO ULTRAVIOLET IRRADIATION |
title_full | THE EFFECT OF HYDROCORTISONE ON THE RESPONSE OF FETAL RAT SKIN IN CULTURE TO ULTRAVIOLET IRRADIATION |
title_fullStr | THE EFFECT OF HYDROCORTISONE ON THE RESPONSE OF FETAL RAT SKIN IN CULTURE TO ULTRAVIOLET IRRADIATION |
title_full_unstemmed | THE EFFECT OF HYDROCORTISONE ON THE RESPONSE OF FETAL RAT SKIN IN CULTURE TO ULTRAVIOLET IRRADIATION |
title_short | THE EFFECT OF HYDROCORTISONE ON THE RESPONSE OF FETAL RAT SKIN IN CULTURE TO ULTRAVIOLET IRRADIATION |
title_sort | effect of hydrocortisone on the response of fetal rat skin in culture to ultraviolet irradiation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2137545/ https://www.ncbi.nlm.nih.gov/pubmed/14005935 |
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