EFFECTS OF ENTERIC MICROBIAL OVERGROWTH ON SMALL INTESTINAL ULTRASTRUCTURE IN RAT
- 1 January 1978
- journal article
- research article
- Vol. 70 (3) , 249-258
Abstract
Ultrastructural effects of bacterial proliferation in the upper gastrointestinal tract induced by i.p. injections of mecamylamine HCl were investigated in rats. Increased populations of nonspecific enteric bacteria were found in the lumen of the upper small intestine and ultrastructural abnormalities in the absorptive epithelial cells, including increased numbers of lysosomal vacuoles, fused microvilli and dilated endoplasmic reticulum. The bacteria did not penetrate into the damaged mucosal cells and so cytoplasmic infiltration is not required to cause ultrastructural changes. Alterations were not merely due to the pharmacologic agent used. Rats with subnormal numbers of enteric bacteria in the upper small intestine, whether subjected to the course of the drug or not, did not display observed ultrastructural changes. Concomitant with increased numbers of enteric bacteria in the small intestine, there were increased concentrations of deconjugated bile salts and decreased absorption of glucose. Apparently the hypothetical sequence of pathogenesis is mecamylamine, intestinal stasis, bacterial overgrowth, deconjugation of the bile salts and ultrastructural alterations.This publication has 6 references indexed in Scilit:
- Effects of Anionic Surfactants on Hamster Small Intestinal Membrane Structure and Function: Relationship to Surface ActivityGastroenterology, 1977
- The role of altered bile acid metabolism in the steatorrhea of experimental blind loop.Journal of Clinical Investigation, 1966
- PATHOGENESIS OF ACUTE CLINICAL DIARRHEAL DISEASE1965
- Diarrheal Diseases of ChildrenAmerican Journal of Diseases of Children, 1964
- Bacteriological and histological studies of the small intestine of rats treated with mecamylamineGut, 1963
- The determination of bile acids in bile and duodenal contents by quantitative paper chromatography bile acids and steroids 71Clinica Chimica Acta; International Journal of Clinical Chemistry, 1959