Literature DB >> 6474008

The fate of lipopolysaccharide in rats: evidence for chemical alteration in the molecule.

M A Freudenberg, B Kleine, C Galanos.   

Abstract

The fate of smooth form lipopolysaccharide (LPS) from Salmonella abortus-equi injected intravenously in rats was studied. In the circulation, the LPS formed a stabile complex with high density plasma lipoprotein and was cleared from the blood primarily into the liver at a slow rate (over a period of two days). In the liver, LPS was first detectable in Kupffer's cells and granulocytes; from there it was later redistributed (after two days) into hepatocytes. While it was in the circulation, no evidence for alteration in the chemical structure of the LPS was found. However, partial loss of fatty acids occurred in the liver and also other organs such as the spleen. The excretion of chemically altered LPS continued for several weeks, mainly via the feces and, to a small extent, in the urine.

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Year:  1984        PMID: 6474008     DOI: 10.1093/clinids/6.4.483

Source DB:  PubMed          Journal:  Rev Infect Dis        ISSN: 0162-0886


  16 in total

1.  Comparative studies of endotoxin uptake by isolated rat Kupffer and peritoneal cells.

Authors:  E S Fox; P Thomas; S A Broitman
Journal:  Infect Immun       Date:  1987-12       Impact factor: 3.441

Review 2.  Immunoprophylaxis and immunotherapy of gram-negative sepsis and shock with antibodies to core glycolipids and lipid A of bacterial lipopolysaccharides.

Authors:  I G Mitov; D G Terziiski
Journal:  Infection       Date:  1991 Nov-Dec       Impact factor: 3.553

3.  Structural changes produced in Kupffer cells in the rat liver by injection of lipopolysaccharide.

Authors:  H Van Bossuyt; E Wisse
Journal:  Cell Tissue Res       Date:  1988-01       Impact factor: 5.249

4.  Changes in endotoxin-binding proteins during major elective surgery: important role for soluble CD14 in regulation of biological activity of systemic endotoxin.

Authors:  N Hiki; D Berger; M A Dentener; Y Mimura; W A Buurman; C Prigl; M Seidelmann; E Tsuji; M Kaminishi; H G Beger
Journal:  Clin Diagn Lab Immunol       Date:  1999-11

5.  Endotoxin binding and elimination by monocytes: secretion of soluble CD14 represents an inducible mechanism counteracting reduced expression of membrane CD14 in patients with sepsis and in a patient with paroxysmal nocturnal hemoglobinuria.

Authors:  N Hiki; D Berger; C Prigl; E Boelke; H Wiedeck; M Seidelmann; L Staib; M Kaminishi; T Oohara; H G Beger
Journal:  Infect Immun       Date:  1998-03       Impact factor: 3.441

6.  The role of macrophages in LPS-induced lethality and tissue injury.

Authors:  P H Groeneveld; E Claassen; C F Kuper; N Van Rooijen
Journal:  Immunology       Date:  1988-03       Impact factor: 7.397

7.  Response of cultured rat Kupffer cells to lipopolysaccharide.

Authors:  H Van Bossuyt; C Desmaretz; B Rombaut; E Wisse
Journal:  Arch Toxicol       Date:  1988       Impact factor: 5.153

8.  Yersinia lipopolysaccharide is modified by human monocytes.

Authors:  M Wuorela; S Jalkanen; P Toivanen; K Granfors
Journal:  Infect Immun       Date:  1993-12       Impact factor: 3.441

Review 9.  Receptors, mediators, and mechanisms involved in bacterial sepsis and septic shock.

Authors:  Edwin S Van Amersfoort; Theo J C Van Berkel; Johan Kuiper
Journal:  Clin Microbiol Rev       Date:  2003-07       Impact factor: 26.132

10.  Chylomicrons enhance endotoxin excretion in bile.

Authors:  T E Read; H W Harris; C Grunfeld; K R Feingold; M C Calhoun; J P Kane; J H Rapp
Journal:  Infect Immun       Date:  1993-08       Impact factor: 3.441

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