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PMID: 7164114 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Biochemical and pathological effects of Clostridium difficile toxins in mice.

Toxicon : official journal of the International Society on Toxinology ·Vol. 20 ·No. 6 ·1982-00-00 ·Pages 983-9

Ehrich M

Abstract

Toxins produced by Clostridium difficile are lethal to mice after i.p. administration. Among the alterations observed when mice were given a preparation containing both Toxin A and Toxin B were a 1.6 +/- 0.2 degrees C (mean +/- S.E., N = 7) depression of rectal body temperature, blood in the liver (318 +/- 13% of control levels) and a decrease in glutathione concentration (74 +/- 2% of control). Purified Toxin A and purified Toxin B were both able to alter these parameters. Toxin B, however, had a more profound effect on serum isocitrate dehydrogenase levels (raised to 198 +/- 18% of control) and liver O-demethylase activity (reduced to 64 +/- 8% of control), parameters sensitive to alteration in liver damage. The effects of Toxin B on these parameters were partially alleviated in mice pretreated with N-acetylcysteine (1.2 g/kg i.p.) and triamcinolone (120 mg/kg i.p.) and, although the percentage of survivors did not improve, survival time was increased from 3.0 +/- 0.1 hr to 4.6 +/- 0.5 and 5.7 +/- 1.3 hr, respectively, by these agents.

MeSH Terms
Animals Bacterial Toxins/toxicity Body Temperature/drug effects Clostridium/pathogenicity Glutathione/analysis Isocitrate Dehydrogenase/blood Liver/analysis,drug effects Male Mice Mice, Inbred ICR Phenothiazines/pharmacology Triamcinolone/pharmacology
Chemicals
Bacterial Toxins Phenothiazines Triamcinolone Isocitrate Dehydrogenase Glutathione
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Ehrich M
Article Info
Journal
Toxicon : official journal of the International Society on Toxinology
Abbr.
Toxicon
ISSN
0041-0101
Published
1982-00-00
Pages
983-9
Language
English
Region
England
NLM ID
1307333
Subset
IM
Grants
PHS HHS · 363183 · United States
NIAID NIH HHS · AI-15749-03 · United States
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