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Am J Physiol Regul Integr Comp Physiol 286: R699-R709, 2004. First published January 8, 2004; doi:10.1152/ajpregu.00593.2003
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INFLAMMATION, CYTOKINES, AND TEMPERATURE REGULATION

Lethality during continuous anthrax lethal toxin infusion is associated with circulatory shock but not inflammatory cytokine or nitric oxide release in rats

Xizhong Cui,1 Mahtab Moayeri,2 Yan Li,1 Xuemei Li,1 Michael Haley,1 Yvonne Fitz,1 Rosaly Correa-Araujo,1 Steven M. Banks,1 Stephen H. Leppla,2 and Peter Q. Eichacker1

1Critical Care Medicine Department, Clinical Center, National Institutes of Health; and 2National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892

Submitted 10 October 2003 ; accepted in final form 30 December 2003

Although circulatory shock related to lethal toxin (LeTx) may play a primary role in lethality due to Bacillus anthracis infection, its mechanisms are unclear. We investigated whether LeTx-induced shock is associated with inflammatory cytokine and nitric oxide (NO) release. Sprague-Dawley rats with central venous and arterial catheters received 24-h infusions of LeTx (lethal factor 100 µg/kg; protective antigen 200 µg/kg) that produced death beginning at 9 h and a 7-day mortality rate of 53%. By 9 h, mean arterial blood pressure, heart rate, pH, and base excess were decreased and lactate and hemoglobin levels were increased in LeTx nonsurvivors compared with LeTx survivors and controls (diluent only) (P <= 0.05 for each comparing the 3 groups). Despite these changes, arterial oxygen and circulating leukocytes and platelets were not decreased and TNF-{alpha}, IL-1{beta}, IL-6, and IL-10 levels were not increased comparing either LeTx nonsurvivors or survivors to controls. Nitrate/nitrite levels and tissue histology also did not differ comparing LeTx animals and controls. In additional experiments, although 24-h infusions of LeTx and Esherichia coli LPS produced similar mortality rates (54 and 56%, respectively) and times to death (13.2 ± 0.8 vs. 11.0 ± 1.7 h, respectively) compared with controls, only LPS reduced circulating leukocytes, platelets, and IL-2 levels and increased TNF-{alpha}, IL-1{alpha} and -1{beta}, IL-6, IL-10, interferon-{gamma}, granulocyte macrophage-colony stimulating factor, RANTES, migratory inhibitory protein-1{alpha}, -2, and -3, and monocyte chemotactic protein-1, as well as nitrate/nitrite levels (all P <= 0.05 for the effects of LPS). Thus, in contrast to LPS, excessive inflammatory cytokine and NO release does not appear to contribute to the circulatory shock and lethality occurring with LeTx in this rat model. Although therapies to modulate these host mediators may be applicable for shock caused by LPS or other bacterial toxins, they may not with LeTx.

Bacillus anthracis; sepsis; pathogenesis; model


Address for reprint requests and other correspondence: X. Cui, Critical Care Medicine Dept., National Institutes of Health, Bldg. 10, Rm. 7D43, Bethesda, MD 20892 (cxizhong{at}mail.cc.nih.gov).




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