Literature DB >> 4005148

Excretion of radioactivity in faeces and urine of rats injected with 3H,14C-lipopolysaccharide.

B Kleine, M A Freudenberg, C Galanos.   

Abstract

The route of excretion of lipopolysaccharide (LPS) and its possible degradation in vivo was studied in rats using biosynthetically radiolabelled LPS from Salmonella abortus equi, carrying 3H activity exclusively in fatty acids and 14C activity in fatty acids and sugars. Following intravenous injection of the above LPS in AS2 rats with or without anaesthesia, excretion of radioactivity occurred mainly in the faeces and to smaller extent in urine. The rate of excretion was slow, a large part of the radioactivity being still present in the liver after 14 days. In faeces the percent recovery of 3H (18%) was lower than that of 14C (32%) suggesting loss of tritium activity and thereby of fatty acids from the excreted LPS. A similar loss of tritium was also found in the material remaining in the liver and spleen 14 days after LPS administration. In urine the material recovered during 14 days (about 7% of injected) was different from the original LPS, 70% of 14C activity being dialysable and practically all 3H activity being volatile. Similar results were also obtained following administration of the LPS intraperitoneally under anaesthesia. However, when the LPS was administered intraperitoneally without anaesthesia, in the majority of the animals, 90% of 14C and 54% of 3H was excreted in faeces within 3 days, suggesting that both route of administration and use of anaesthesia during injection influence the subsequent rate of excretion of LPS.

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Year:  1985        PMID: 4005148      PMCID: PMC2041064     

Source DB:  PubMed          Journal:  Br J Exp Pathol        ISSN: 0007-1021


  11 in total

1.  Inactivation of endotoxin by a humoral component. VII. Enzymatic degradation of endotoxin by blood plasma.

Authors:  W R KEENE; M LANDY; M J SHEAR
Journal:  J Clin Invest       Date:  1961-02       Impact factor: 14.808

2.  Host defense against bacterial endotoxemia-contribution of the early and late components of complement to detoxification.

Authors:  J E May; M A Kane; M M Frank
Journal:  J Immunol       Date:  1972-10       Impact factor: 5.422

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Journal:  Eur J Biochem       Date:  1969-01

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Authors:  J A Rudbach; R L Anacker; W T Haskins; A G Johnson; K C Milner; E Ribi
Journal:  Ann N Y Acad Sci       Date:  1966-06-30       Impact factor: 5.691

5.  The essential role of the liver in detoxification of endotoxin.

Authors:  W E Farrar; L M Corwin
Journal:  Ann N Y Acad Sci       Date:  1966-06-30       Impact factor: 5.691

6.  Time course of cellular distribution of endotoxin in liver, lungs and kidneys of rats.

Authors:  M A Freudenberg; N Freudenberg; C Galanos
Journal:  Br J Exp Pathol       Date:  1982-02

7.  Interaction of lipopolysaccharides with plasma high-density lipoprotein in rats.

Authors:  M A Freudenberg; T C Bøg-Hansen; U Back; C Galanos
Journal:  Infect Immun       Date:  1980-05       Impact factor: 3.441

8.  Enzymatic deacylation of the lipid A moiety of Salmonella typhimurium lipopolysaccharides by human neutrophils.

Authors:  C L Hall; R S Munford
Journal:  Proc Natl Acad Sci U S A       Date:  1983-11       Impact factor: 11.205

9.  Isolation from human serum of an inactivator of bacterial lipopolysaccharide.

Authors:  K J Johnson; P A Ward; S Goralnick; M J Osborn
Journal:  Am J Pathol       Date:  1977-09       Impact factor: 4.307

10.  The mitogenic effect of lipopolysaccharide on bone marrow-derived mouse lymphocytes. Lipid A as the mitogenic part of the molecule.

Authors:  J Andersson; F Melchers; C Galanos; O Lüderitz
Journal:  J Exp Med       Date:  1973-04-01       Impact factor: 14.307

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  6 in total

1.  Induction of tolerance to lipopolysaccharide (LPS)-D-galactosamine lethality by pretreatment with LPS is mediated by macrophages.

Authors:  M A Freudenberg; C Galanos
Journal:  Infect Immun       Date:  1988-05       Impact factor: 3.441

2.  Dephosphorylation of the lipid A moiety of Escherichia coli lipopolysaccharide by mouse macrophages.

Authors:  A A Peterson; R S Munford
Journal:  Infect Immun       Date:  1987-04       Impact factor: 3.441

3.  Deacylation of bacterial lipopolysaccharide in rat hepatocytes in vitro.

Authors:  I Fukuda; K Tanamoto; S Kanegasaki; Y Yajima; Y Goto
Journal:  Br J Exp Pathol       Date:  1989-06

4.  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

5.  Adenovirus-mediated transfer of a gene encoding acyloxyacyl hydrolase (AOAH) into mice increases tissue and plasma AOAH activity.

Authors:  M G Coulthard; J Swindle; R S Munford; R D Gerard; R S Meidell
Journal:  Infect Immun       Date:  1996-05       Impact factor: 3.441

6.  Falcarinol Is a Potent Inducer of Heme Oxygenase-1 and Was More Effective than Sulforaphane in Attenuating Intestinal Inflammation at Diet-Achievable Doses.

Authors:  Amanda L Stefanson; Marica Bakovic
Journal:  Oxid Med Cell Longev       Date:  2018-10-21       Impact factor: 6.543

  6 in total

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