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EFFECTS OF NEOMYCIN AND PENICILLIN ADMINISTRATION ON MUCOSAL PROLIFERATION OF THE MOUSE SMALL INTESTINE : WITH MORPHOLOGICAL AND FUNCTIONAL CORRELATIONS

The effects of an oral neomycin and penicillin regimen on intestinal bacteriology and on morphology and function of the small intestine of mice were investigated. Quantitative and qualitative stool cultures on selective media of the treated animals revealed only growth of yeast organisms. The treate...

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Autores principales: Khoury, Kenneth A., Floch, Martin H., Herskovic, Teodoro
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1969
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2138647/
https://www.ncbi.nlm.nih.gov/pubmed/4388518
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author Khoury, Kenneth A.
Floch, Martin H.
Herskovic, Teodoro
author_facet Khoury, Kenneth A.
Floch, Martin H.
Herskovic, Teodoro
author_sort Khoury, Kenneth A.
collection PubMed
description The effects of an oral neomycin and penicillin regimen on intestinal bacteriology and on morphology and function of the small intestine of mice were investigated. Quantitative and qualitative stool cultures on selective media of the treated animals revealed only growth of yeast organisms. The treated animals developed enlargement of the ceca with fluid contents and watery stools, resembling characteristics of germfree animals. Radioautography with tritiated thymidine revealed an increased epithelial cell migration rate in the mice treated with the antibiotics for 3 to 5 wk. A slight increase in villus height was also noted. The treated male mice showed greater variance than the treated females in epithelial cell migration rates. Histochemical staining reactions showed a decrease in nonspecific esterase and in NADH dehydrogenase activity in the proximal gut of the antibiotic animals. Stains of distal gut and those for acid and alkaline phosphatase, NADPH dehydrogenase, lactic dehydrogenase, and succinic dehydrogenase were similar to the controls. A slight increase in sucrase activity and a slight decrease in lactase activity in the antibiotic animals was observed in contrast to control animals. Germfree mice, however, had greater sucrase and lactase activity. Transport of L-methionine was slightly reduced in the distal segment of the treated animals. Since the direction of these changes is away from the intestinal state observed in germfree animals, they are probably the result of the direct action of the antibiotics on the gut.
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spelling pubmed-21386472008-04-17 EFFECTS OF NEOMYCIN AND PENICILLIN ADMINISTRATION ON MUCOSAL PROLIFERATION OF THE MOUSE SMALL INTESTINE : WITH MORPHOLOGICAL AND FUNCTIONAL CORRELATIONS Khoury, Kenneth A. Floch, Martin H. Herskovic, Teodoro J Exp Med Article The effects of an oral neomycin and penicillin regimen on intestinal bacteriology and on morphology and function of the small intestine of mice were investigated. Quantitative and qualitative stool cultures on selective media of the treated animals revealed only growth of yeast organisms. The treated animals developed enlargement of the ceca with fluid contents and watery stools, resembling characteristics of germfree animals. Radioautography with tritiated thymidine revealed an increased epithelial cell migration rate in the mice treated with the antibiotics for 3 to 5 wk. A slight increase in villus height was also noted. The treated male mice showed greater variance than the treated females in epithelial cell migration rates. Histochemical staining reactions showed a decrease in nonspecific esterase and in NADH dehydrogenase activity in the proximal gut of the antibiotic animals. Stains of distal gut and those for acid and alkaline phosphatase, NADPH dehydrogenase, lactic dehydrogenase, and succinic dehydrogenase were similar to the controls. A slight increase in sucrase activity and a slight decrease in lactase activity in the antibiotic animals was observed in contrast to control animals. Germfree mice, however, had greater sucrase and lactase activity. Transport of L-methionine was slightly reduced in the distal segment of the treated animals. Since the direction of these changes is away from the intestinal state observed in germfree animals, they are probably the result of the direct action of the antibiotics on the gut. The Rockefeller University Press 1969-05-01 /pmc/articles/PMC2138647/ /pubmed/4388518 Text en Copyright © 1969 by The Rockefeller University Press 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
Khoury, Kenneth A.
Floch, Martin H.
Herskovic, Teodoro
EFFECTS OF NEOMYCIN AND PENICILLIN ADMINISTRATION ON MUCOSAL PROLIFERATION OF THE MOUSE SMALL INTESTINE : WITH MORPHOLOGICAL AND FUNCTIONAL CORRELATIONS
title EFFECTS OF NEOMYCIN AND PENICILLIN ADMINISTRATION ON MUCOSAL PROLIFERATION OF THE MOUSE SMALL INTESTINE : WITH MORPHOLOGICAL AND FUNCTIONAL CORRELATIONS
title_full EFFECTS OF NEOMYCIN AND PENICILLIN ADMINISTRATION ON MUCOSAL PROLIFERATION OF THE MOUSE SMALL INTESTINE : WITH MORPHOLOGICAL AND FUNCTIONAL CORRELATIONS
title_fullStr EFFECTS OF NEOMYCIN AND PENICILLIN ADMINISTRATION ON MUCOSAL PROLIFERATION OF THE MOUSE SMALL INTESTINE : WITH MORPHOLOGICAL AND FUNCTIONAL CORRELATIONS
title_full_unstemmed EFFECTS OF NEOMYCIN AND PENICILLIN ADMINISTRATION ON MUCOSAL PROLIFERATION OF THE MOUSE SMALL INTESTINE : WITH MORPHOLOGICAL AND FUNCTIONAL CORRELATIONS
title_short EFFECTS OF NEOMYCIN AND PENICILLIN ADMINISTRATION ON MUCOSAL PROLIFERATION OF THE MOUSE SMALL INTESTINE : WITH MORPHOLOGICAL AND FUNCTIONAL CORRELATIONS
title_sort effects of neomycin and penicillin administration on mucosal proliferation of the mouse small intestine : with morphological and functional correlations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2138647/
https://www.ncbi.nlm.nih.gov/pubmed/4388518
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