Endotoxin inhibitor prevents sepsis-induced alterations in intestinal ion transport

Am J Surg. 1996 Oct;172(4):341-4. doi: 10.1016/S0002-9610(96)00189-4.

Abstract

Background: The intestine is a target of septic insult. The aims of this study were to characterize sepsis-induced alterations in intestinal ion transport and to determine the role endotoxin plays in mediating these changes.

Methods: Rats underwent cecal manipulation alone (control), cecal ligation and puncture (CLP), or CLP plus intraperitoneal injection of 0.2 mg of a recently synthesized endotoxin inhibitor. At 24 hours, distal ileum was harvested, and transport parameters were determined.

Results: Cecal ligation and puncture produced a significant increase in short-circuit current (Isc) that was attributable to the induction of chloride secretion. There were no alterations in transepithelial resistance or fluxes of mannitol and sodium. The sepsis-induced increase in Isc was prevented by administration of the endotoxin inhibitor.

Conclusions: In this model of sepsis, the primary alteration in ileal ion transport is an induction of electrogenic chloride secretion. Endotoxin inhibition may represent a strategy for prophylaxis against the intestinal effects of sepsis.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Cecum / injuries
  • Cecum / surgery
  • Disease Models, Animal
  • Endotoxins / antagonists & inhibitors*
  • Enteritis / metabolism*
  • In Vitro Techniques
  • Intestinal Mucosa / drug effects
  • Intestinal Mucosa / metabolism*
  • Ion Transport / drug effects
  • Ligation
  • Permeability / drug effects
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Endotoxins