Cargando…

THE PATHOGENESIS OF EXPERIMENTAL COLITIS, AND THE RELATION OF COLITIS IN ANIMALS AND MAN

1. The facts described in this paper are intended to bear upon the pathogenesis of colitis in man and animals. 2. The toxin of the Shiga dysentery bacillus is liberated from the bacillus through the process of autolysis. 3. In rabbits the toxin is not absorbed directly in an active form by the gastr...

Descripción completa

Detalles Bibliográficos
Autores principales: Flexner, Simon, Sweet, J. Edwin
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1906
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2124634/
https://www.ncbi.nlm.nih.gov/pubmed/19867056
_version_ 1782141707732647936
author Flexner, Simon
Sweet, J. Edwin
author_facet Flexner, Simon
Sweet, J. Edwin
author_sort Flexner, Simon
collection PubMed
description 1. The facts described in this paper are intended to bear upon the pathogenesis of colitis in man and animals. 2. The toxin of the Shiga dysentery bacillus is liberated from the bacillus through the process of autolysis. 3. In rabbits the toxin is not absorbed directly in an active form by the gastro-intestinal tract; in man, however, absorption of an active poison does take place from the intestine. 4. The toxin is excreted in rabbits, and probably in man as well by the intestine, chiefly probably by the large intestine, which being injured by the act of elimination, reacts by the development of inflammation, etc. 5. In rabbits the characteristic action of the toxin depends upon the integrity of the biliary secretion into the intestine. When the bile is prevented from entering the intestine, either by ligature and section of the duct or by establishment of a biliary fistula, no lesions whatever of the large intestine appear, or they are inconsiderable in extent. 6. The loss of toxin through a biliary fistula does not prevent in rabbits the lethal effects which are caused, apparently, by a nervous poison. The tying off of the bile duct seems to prevent the passage of the toxin, in amounts sufficient to cause the large intestinal lesions, into the blood. The liver, therefore, in this condition tends to hold back the toxin from the general circulation. 7. The peculiar effects of the toxin on the large intestine in rabbits is not produced at once, but would appear to depend upon successive acts of excretion of the poison by the bowel. 8. The establishment of biliary fistula reduces the intensity of action of corrosive sublimate upon the large intestine in rabbits; and the lesions of ricin poisoning in these animals are also modified by this operation. 9. Dysentery toxin is destroyed by peptic digestion, and also, though probably more slowly, by tryptic digestion. The absence of power of the toxin to cause poisoning in rabbits when it is brought directly into the lumen of the intestine, is not explained by the destructive action of trypsin. 10. The character of the histological changes in the cæcum of rabbits caused by the dysentery toxin points to an action upon the substance and not primarily upon the surface of the intestine.
format Text
id pubmed-2124634
institution National Center for Biotechnology Information
language English
publishDate 1906
publisher The Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-21246342008-04-18 THE PATHOGENESIS OF EXPERIMENTAL COLITIS, AND THE RELATION OF COLITIS IN ANIMALS AND MAN Flexner, Simon Sweet, J. Edwin J Exp Med Article 1. The facts described in this paper are intended to bear upon the pathogenesis of colitis in man and animals. 2. The toxin of the Shiga dysentery bacillus is liberated from the bacillus through the process of autolysis. 3. In rabbits the toxin is not absorbed directly in an active form by the gastro-intestinal tract; in man, however, absorption of an active poison does take place from the intestine. 4. The toxin is excreted in rabbits, and probably in man as well by the intestine, chiefly probably by the large intestine, which being injured by the act of elimination, reacts by the development of inflammation, etc. 5. In rabbits the characteristic action of the toxin depends upon the integrity of the biliary secretion into the intestine. When the bile is prevented from entering the intestine, either by ligature and section of the duct or by establishment of a biliary fistula, no lesions whatever of the large intestine appear, or they are inconsiderable in extent. 6. The loss of toxin through a biliary fistula does not prevent in rabbits the lethal effects which are caused, apparently, by a nervous poison. The tying off of the bile duct seems to prevent the passage of the toxin, in amounts sufficient to cause the large intestinal lesions, into the blood. The liver, therefore, in this condition tends to hold back the toxin from the general circulation. 7. The peculiar effects of the toxin on the large intestine in rabbits is not produced at once, but would appear to depend upon successive acts of excretion of the poison by the bowel. 8. The establishment of biliary fistula reduces the intensity of action of corrosive sublimate upon the large intestine in rabbits; and the lesions of ricin poisoning in these animals are also modified by this operation. 9. Dysentery toxin is destroyed by peptic digestion, and also, though probably more slowly, by tryptic digestion. The absence of power of the toxin to cause poisoning in rabbits when it is brought directly into the lumen of the intestine, is not explained by the destructive action of trypsin. 10. The character of the histological changes in the cæcum of rabbits caused by the dysentery toxin points to an action upon the substance and not primarily upon the surface of the intestine. The Rockefeller University Press 1906-08-01 /pmc/articles/PMC2124634/ /pubmed/19867056 Text en Copyright © Copyright, 1906, 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
Flexner, Simon
Sweet, J. Edwin
THE PATHOGENESIS OF EXPERIMENTAL COLITIS, AND THE RELATION OF COLITIS IN ANIMALS AND MAN
title THE PATHOGENESIS OF EXPERIMENTAL COLITIS, AND THE RELATION OF COLITIS IN ANIMALS AND MAN
title_full THE PATHOGENESIS OF EXPERIMENTAL COLITIS, AND THE RELATION OF COLITIS IN ANIMALS AND MAN
title_fullStr THE PATHOGENESIS OF EXPERIMENTAL COLITIS, AND THE RELATION OF COLITIS IN ANIMALS AND MAN
title_full_unstemmed THE PATHOGENESIS OF EXPERIMENTAL COLITIS, AND THE RELATION OF COLITIS IN ANIMALS AND MAN
title_short THE PATHOGENESIS OF EXPERIMENTAL COLITIS, AND THE RELATION OF COLITIS IN ANIMALS AND MAN
title_sort pathogenesis of experimental colitis, and the relation of colitis in animals and man
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2124634/
https://www.ncbi.nlm.nih.gov/pubmed/19867056
work_keys_str_mv AT flexnersimon thepathogenesisofexperimentalcolitisandtherelationofcolitisinanimalsandman
AT sweetjedwin thepathogenesisofexperimentalcolitisandtherelationofcolitisinanimalsandman
AT flexnersimon pathogenesisofexperimentalcolitisandtherelationofcolitisinanimalsandman
AT sweetjedwin pathogenesisofexperimentalcolitisandtherelationofcolitisinanimalsandman