Home LiteratureArticle Details
PMID: 10070057 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Enteropathogenic E. coli attenuates secretagogue-induced net intestinal ion transport but not Cl- secretion.

The American journal of physiology ·Vol. 276 ·No. 3 ·1999-00-00 ·Pages G781-8

Hecht G, Koutsouris A

Abstract

Enteric bacterial pathogens often increase intestinal Cl- secretion. Enteropathogenic Escherichia coli (EPEC) does not stimulate active ion secretion. In fact, EPEC infection decreases net ion transport in response to classic secretagogues. This has been presumed to reflect diminished Cl- secretion. The aim of this study was to investigate the influence of EPEC infection on specific intestinal epithelial ion transport processes. T84 cell monolayers infected with EPEC were used for these studies. EPEC infection significantly decreased short-circuit current (Isc) in response to carbachol and forskolin, yet 125I efflux studies revealed no difference in Cl- channel activity. There was also no alteration in basolateral K+ channel or Na+-K+-2Cl- cotransport activity. Furthermore, net 36Cl- flux was not decreased by EPEC. No alterations in either K+ or Na+ transport could be demonstrated. Instead, removal of basolateral bicarbonate from uninfected monolayers yielded an Isc response approximating that observed with EPEC infection, whereas bicarbonate removal from EPEC-infected monolayers further diminished Isc. These studies suggest that the reduction in stimulated Isc is not secondary to diminished Cl- secretion. Alternatively, bicarbonate-dependent transport processes appear to be perturbed.

MeSH Terms
Absorption/physiology Bicarbonates/metabolism Biological Transport/physiology Carbachol/pharmacology Cell Line Cell Membrane/metabolism Chlorides/metabolism Colforsin/pharmacology Electric Conductivity Escherichia coli/physiology Escherichia coli Infections/metabolism,physiopathology Humans Intestinal Mucosa/metabolism,microbiology,pathology,physiology Intestines/cytology,physiology Ions Potassium/metabolism Sodium/antagonists & inhibitors,metabolism
Chemicals
Bicarbonates Chlorides Ions Colforsin Carbachol Sodium Potassium
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Hecht G
Department of Medicine, Section of Digestive and Liver Diseases, University of Illinois and West Side Veterans Affairs Medical Center, Chicago, Illinois 60612, USA. gahecht@uic.edu
Koutsouris A
Article Info
Journal
The American journal of physiology
Abbr.
Am J Physiol
ISSN
0002-9513
Published
1999-00-00
Pages
G781-8
Language
English
Region
United States
NLM ID
0370511
Subset
IM
Grants
NIDDK NIH HHS · DK-50694 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com