Cargando…
SEROTOXIN : STUDIES ON FERMENT ACTION. XIV.
1. Sera from which the protective lipoids (unsaturated fatty acids) have been removed are toxic for the homologous animal. 2. The toxicity is due to three factors: (a) an alteration in the mechanism of coagulation, with resulting intravascular coagulation; (b) the exposure of the native serum protei...
Autores principales: | , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
1914
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2125189/ https://www.ncbi.nlm.nih.gov/pubmed/19867787 |
_version_ | 1782141838878048256 |
---|---|
author | Jobling, James W. Petersen, William |
author_facet | Jobling, James W. Petersen, William |
author_sort | Jobling, James W. |
collection | PubMed |
description | 1. Sera from which the protective lipoids (unsaturated fatty acids) have been removed are toxic for the homologous animal. 2. The toxicity is due to three factors: (a) an alteration in the mechanism of coagulation, with resulting intravascular coagulation; (b) the exposure of the native serum proteins; (c) the formation of toxic split products (primary proteoses) by autolysis. 3. A definite maximum of toxicity can be determined, with a final stage of atoxicity due to continued autolysis. 4. Hirudin and sodium citrate do not protect animals. 5. Heating to 70° C. destroys, or greatly lessens, the toxicity of the serotoxin, although the isolated proteoses are toxic after boiling. 6. The return of the extracted lipoids (saponified) neutralizes the toxicity. 7. Unsaturated soaps also neutralize the toxicity. 8. Sublethal doses produce extreme prostration, marked fall in body temperature, no eosinophilia, and an increase of antitrypsin. 9. Sublethal doses of rapidly prepared chloroform sera cause a decrease in coagulation time; sublethal doses of autolyzed sera cause an increase in coagulation time. 10. Previously injected animals are more resistant (increased antiferments). 11. Iodized animals are less resistant (decreased antiferments). |
format | Text |
id | pubmed-2125189 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1914 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21251892008-04-18 SEROTOXIN : STUDIES ON FERMENT ACTION. XIV. Jobling, James W. Petersen, William J Exp Med Article 1. Sera from which the protective lipoids (unsaturated fatty acids) have been removed are toxic for the homologous animal. 2. The toxicity is due to three factors: (a) an alteration in the mechanism of coagulation, with resulting intravascular coagulation; (b) the exposure of the native serum proteins; (c) the formation of toxic split products (primary proteoses) by autolysis. 3. A definite maximum of toxicity can be determined, with a final stage of atoxicity due to continued autolysis. 4. Hirudin and sodium citrate do not protect animals. 5. Heating to 70° C. destroys, or greatly lessens, the toxicity of the serotoxin, although the isolated proteoses are toxic after boiling. 6. The return of the extracted lipoids (saponified) neutralizes the toxicity. 7. Unsaturated soaps also neutralize the toxicity. 8. Sublethal doses produce extreme prostration, marked fall in body temperature, no eosinophilia, and an increase of antitrypsin. 9. Sublethal doses of rapidly prepared chloroform sera cause a decrease in coagulation time; sublethal doses of autolyzed sera cause an increase in coagulation time. 10. Previously injected animals are more resistant (increased antiferments). 11. Iodized animals are less resistant (decreased antiferments). The Rockefeller University Press 1914-05-01 /pmc/articles/PMC2125189/ /pubmed/19867787 Text en Copyright © Copyright, 1914, 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 Jobling, James W. Petersen, William SEROTOXIN : STUDIES ON FERMENT ACTION. XIV. |
title | SEROTOXIN : STUDIES ON FERMENT ACTION. XIV. |
title_full | SEROTOXIN : STUDIES ON FERMENT ACTION. XIV. |
title_fullStr | SEROTOXIN : STUDIES ON FERMENT ACTION. XIV. |
title_full_unstemmed | SEROTOXIN : STUDIES ON FERMENT ACTION. XIV. |
title_short | SEROTOXIN : STUDIES ON FERMENT ACTION. XIV. |
title_sort | serotoxin : studies on ferment action. xiv. |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2125189/ https://www.ncbi.nlm.nih.gov/pubmed/19867787 |
work_keys_str_mv | AT joblingjamesw serotoxinstudiesonfermentactionxiv AT petersenwilliam serotoxinstudiesonfermentactionxiv |