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PMID: 3183065 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Bacterial lipopolysaccharide-induced intestinal microvascular lesions leading to acute diarrhea.

The Journal of clinical investigation ·Vol. 82 ·No. 5 ·1988-11-00 ·Pages 1714-21

Mathan VI, Penny GR, Mathan MM, Rowley D

Abstract

Subcutaneous challenge of mice with lipopolysaccharide (LPS) from gram negative bacteria, produced an intestinal microvascular lesion causing fluid exudation into the lumen of the intestine and diarrhea. The microvascular lesion was characterized by endothelial cell damage and microthrombi in the venules and capillaries of the intestinal lamina propria. Marker organisms, given orally to challenged mice, grew in the exuded fluid and could invade the mucosa. Intravenous transfer of postchallenge plasma produced the lesion in normal mice and absorption of such plasma by Sepharose coupled to LPS-antibody abolished this effect. Instillation of large quantities of LPS into the lumen of the intestine produced scattered microvascular lesions, although none of these animals developed diarrhea. Since a similar microvascular lesion has been described in the rectal mucosal lamina propria of adults with acute diarrhea, it is suggested that LPS-induced vascular damage may be a novel mechanism in the pathogenesis of acute diarrhea.

MeSH Terms
Acute Disease Animals Antibodies Diarrhea/pathology Endothelium, Vascular/drug effects,pathology Intestines/blood supply,drug effects Lipopolysaccharides/toxicity Mice Microcirculation/drug effects Polymyxin B/pharmacology
Chemicals
Antibodies Lipopolysaccharides Polymyxin B
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Mathan V I
Wellcome Research Unit, Christian Medical College Hospital, Vellore, India.
Penny G R
Mathan M M
Rowley D
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18 references, click to expand
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Article Info
Journal
The Journal of clinical investigation
Abbr.
J Clin Invest
ISSN
0021-9738
Published
1988-11-00
Pages
1714-21
Language
English
Region
United States
NLM ID
7802877
PMCID
PMC442742
Subset
IM
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