Literature DB >> 949180

Enhanced toxicity for mice of combinations of bacterial lipopolysaccharide and vincristine.

A E Munson, D C Drummond, A C Adams, S G Bradley.   

Abstract

Sublethal doses of vincristine (VNC) and bacterial lipopolysaccharide (LPS) administered simultaneously to adult male mice resulted in markedly enhanced mortality. All of 10 strains of Pseudomonas aeruginosa tested, 4 of 7 strains of Bacteroides, and 6 of 10 strains of Listeria monocytogenes were able to substitute for purified LPS in enhancing mortality in VNC-treated mice. Inoculation of mice with each of 10 strains of Pseudomonas, each of 7 strains of Bacteroides, and about half of the 10 strains of Listeria tested elicited increased resistance to the lethal action of purified LPS. The patterns of responses of mice receiving a lethal combination of 2 mg of LPS/kg and 1 mg of VNC/kg resembled those of mice receiving a lethal dose of 10 mg of VNC/kg alone or 15 mg of LPS/kg alone with respect to (i) serum glutamic pyruvate transaminase activity, (ii) hematocrit values, and (iii) thrombocytopenia. The patterns of responses of mice receiving a lethal combination of LPS and VNC resembled those of mice receiving a lethal dose of LPS alone with respect to (i) hypothermia, (ii) retention of sulfobromophthalein, (iii) fibrinogen level, (iv) prothrombin activity, (v) blood urea nitrogen levels, and (vi) time of death. These data are consistent with the proposition that the combination of VNC and LPS produces a fatal renal failure. Histological studies confirmed that there was extensive renal damage in mice treated with lethal doses of LPS alone or a lethal combination of LPS and VNC.

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Year:  1976        PMID: 949180      PMCID: PMC429630          DOI: 10.1128/AAC.9.5.840

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  22 in total

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Review 2.  THE VINCA ALKALOIDS: A NEW CLASS OF ONCOLYTIC AGENTS.

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4.  A new method for the determination of fibrinogen in small samples of plasma.

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Review 5.  Interaction of bacterial toxins in the toxicity of chemotherapeutic agents.

Authors:  W C Rose
Journal:  CRC Crit Rev Toxicol       Date:  1973-09

6.  Evidence against the presence of cyclic AMP and related enzymes in selected strains of Bacteroides fragilis.

Authors:  P B Hylemon; P V Phibbs
Journal:  Biochem Biophys Res Commun       Date:  1974-09-09       Impact factor: 3.575

Review 7.  Infectious complications of neoplastic disease.

Authors:  D Armstrong; L S Young; R D Meyer; A H Blevins
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8.  Biological properties of surface components of Listeria monocytogenes (Ei factor).

Authors:  F Patocka; M Mára; B Potuźníková; A Jirásek; E Mencíková
Journal:  J Hyg Epidemiol Microbiol Immunol       Date:  1974

9.  Enhanced toxicity for mice of 6-mercaptopurine with bacterial endotoxin.

Authors:  N M Marecki; S G Bradley
Journal:  Antimicrob Agents Chemother       Date:  1974-04       Impact factor: 5.191

10.  Enhanced toxicity for mice of vincristine and other chemotherapeutic agents with Salmonella typhosa endotoxin and Pseudomonas aeruginosa.

Authors:  W C Rose; S G Bradley; I P Lee
Journal:  Antimicrob Agents Chemother       Date:  1972-06       Impact factor: 5.191

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  2 in total

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2.  Toxic interactions of benzyl alcohol with bacterial endotoxin.

Authors:  T A Cebula; A N El-Hage; V J Ferrans
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