Literature DB >> 1202594

Protection of the intestinal mucosa during ischaemia by intraluminal perfusion.

V Mirkovitch, H Menge, J W Robinson.   

Abstract

The function of the intestinal mucosa immediately after one hour's ischaemia was examined by means of tests in vivo and in vitro. During the ischaemia, the intestinal loop was perfused with media of different compositions, in an attempt to assess which provided the best protection of the epithelium from the deleterious effects of the ischaemia. The absorption of water, ions and glucose was then monitored in vivo, and the uptake of phenylalanine and beta methyl-glucoside by slices of mucosa was determined in vitro. The unprotected mucosa loses all active transport capacity in vitro following one hour's ischaemia, and is the site of a pronounced loss of water and ions into the lumen in vivo. Glucose absorption in vivo is also abolished. If the loop is perfused during the ischaemia with glucose-containing Krebs bicarbonate buffer, much of the transport capacity in vitro is retained; the loss of ions and water is prevented, and glucose absorption in vivo occurs. Perfusion during the ischaemia with other media, such as isotonic mannitol, Krebs bicarbonate buffer, or Ringer-lactate solution, results in a marked protection of the mucosa, in comparison with the unperfused loop, but the effects are not as pronounced as those of the glucose-containing buffer. It is concluded that the act of perfusing the intestine is the most beneficial factor, but that the presence of glucose in the perfusate does afford added protection.

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Year:  1975        PMID: 1202594     DOI: 10.1007/bf01851184

Source DB:  PubMed          Journal:  Res Exp Med (Berl)        ISSN: 0300-9130


  4 in total

Review 1.  Response of the intestinal mucosa to ischaemia.

Authors:  J W Robinson; V Mirkovitch; B Winistörfer; F Saegesser
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Authors:  Angelina E Altshuler; Michael D Richter; Augusta E Modestino; Alexander H Penn; Michael J Heller; Geert W Schmid-Schönbein
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4.  Transmural intestinal wall permeability in severe ischemia after enteral protease inhibition.

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  4 in total

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