Abstract

Gram-negative septicemia elicits multiple abnormalities of the coagulation system. Although products of coagulation can lead to clot formation, thereby potentiating organ damage, recent work has shown that low concentrations of thrombin can protect animals from the shock state. Because these amounts of thrombin also lead to formation in vivo of the anticoagulant enzyme, activated protein C, we examined the role of protein C in modulation of Escherichia coli shock in baboons. First, we infused activated protein C and lethal concentrations of E. coli organisms, which prevented the coagulopathic, hepatotoxic, and lethal effects of E. coli. Second, using an antibody to protein C we blocked protein C activation in vivo to determine if this influenced the response to lethal and sublethal concentrations of E. coli organisms. Under these conditions the response to lethal concentrations of E. coli organisms was made more severe and the response to sublethal concentrations of E. coli was made lethal. The coagulopathic, hepatotoxic, and lethal responses in this latter case were prevented by infusion of exogenous protein C.

Keywords

Escherichia coliIn vivoLethal doseBaboonMicrobiologyProtein CThrombinCoagulationBiologyDisseminated intravascular coagulationChemistryImmunologyBiochemistryMedicineInternal medicineToxicologyPlateletEndocrinology

Affiliated Institutions

Related Publications

BACTERICIDAL ACTION OF HISTONE

The arginine-rich fraction of calf thymus histone (histone B) exerts bactericidal activity on various coliform bacilli and micrococci under certain conditions in vitro. Final co...

1958 The Journal of Experimental Medicine 357 citations

Publication Info

Year
1987
Type
article
Volume
79
Issue
3
Pages
918-925
Citations
826
Access
Closed

External Links

Social Impact

Social media, news, blog, policy document mentions

Citation Metrics

826
OpenAlex

Cite This

Fletcher B. Taylor, Alvin Chang, CT Esmon et al. (1987). Protein C prevents the coagulopathic and lethal effects of Escherichia coli infusion in the baboon.. Journal of Clinical Investigation , 79 (3) , 918-925. https://doi.org/10.1172/jci112902

Identifiers

DOI
10.1172/jci112902