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Lethal effects and cardiovascular effects of purified alpha- and theta-toxins from Clostridium perfringens.

Abstract
Shock, a common and frequently fatal manifestation of gas gangrene caused by Clostridium perfringens, is probably mediated by extracellular toxins. Previous studies implicating alpha-toxin as the major lethal factor were frequently done with preparations contaminated with a second lethal factor, theta-toxin. We purified alpha- and theta-toxins from C. perfringens and demonstrated that both were lethal to mice. We investigated the effects of these purified toxins on cardiovascular function in intact rabbits; both toxins caused profound hypotension and bradycardia within 40 min. Reduced cardiac output preceded the development of hypotension and bradycardia. Purified alpha-toxin produced a dose-dependent reduction in myocardial function in isolated rabbit atrial preparations. Purified theta-toxin did not directly inhibit myocardial function. Shock induced by alpha-toxin may be partly mediated by direct depression of myocardial function. theta-Toxin reduced cardiac output in intact animals but had no direct effects on isolated heart preparations at concentrations that induced shock in intact animals. These data suggest that theta-toxin-induced shock could be mediated by an endogenous myocardial depressant factor.
AuthorsD L Stevens, B E Troyer, D T Merrick, J E Mitten, R D Olson
JournalThe Journal of infectious diseases (J Infect Dis) Vol. 157 Issue 2 Pg. 272-9 (Feb 1988) ISSN: 0022-1899 [Print] United States
PMID2891775 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.)
Chemical References
  • Bacterial Toxins
  • Calcium-Binding Proteins
  • Hemolysin Proteins
  • Clostridium perfringens theta-toxin
  • Type C Phospholipases
  • alpha toxin, Clostridium perfringens
Topics
  • Animals
  • Bacterial Toxins (toxicity)
  • Blood Pressure (drug effects)
  • Calcium-Binding Proteins
  • Cardiac Output (drug effects)
  • Clostridium perfringens
  • Female
  • Gas Gangrene (complications)
  • Heart (drug effects)
  • Heart Rate (drug effects)
  • Hemodynamics (drug effects)
  • Hemolysin Proteins (toxicity)
  • Male
  • Mice
  • Rabbits
  • Shock, Septic (etiology)
  • Type C Phospholipases

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