Intraperitoneal (ip) injection of lipopolysaccharide (LPS) results in an acute phase response (APR), which includes the development of fever. As a result of recent work from several laboratories, evidence has accumulated that an ip injection of LPS induces fever by causing the release into the circulation of an endogenous pyrogen (EP), possibly interleukin-1 (IL-1), which in turn causes a rise in hypothalamic interleukin-6 (IL-6). Although there are data showing that tumor necrosis factor (TNF) is a pyrogen, most of these studies were based on injection of pharmacological doses of this cytokine. Using neutralizing antibodies or soluble receptors to TNF, Dr. Kluger has generated data showing that TNF might actually be an endogenous cryogen (EC), which limits fever. The purpose of the proposed experiments is to continue our investigations to critically evaluate the degree to which LPS-and bacterial-induced fevers actually involve these and other cytokines both in the circulation and the brain. We hypothesize that some of these cytokines are endogenous pyrogens and others are endogenous antipyretics or cryogens. The balance between the two types of mediators determines the pattern and time-course of fever.
Our specific aims are to continue our studies to investigate: the pyrogenic effects of IL-1, the relationship between IL-1 and IL-6 in fever, the antipyretic or cryogenic actions of TNF, the possible role of other cytokines as endogenous antipyretics or endogenous cryogens, gender differences in febrile responses. These studies will be run in both male and female rats, and in transgenic knock- out mice deficient in the genes for various cytokines or cytokine receptors. One of the difficulties in studying the precise roles of cytokines in fever has been the inability to selectively block the biological actions of specific cytokines. With the advent of recombinant cytokines, the development of antibodies and other specific blockers, and the availability of transgenic knock-out mice, it is now possible to assess the roles of cytokines in the fever.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
7R01AI027556-10
Application #
6214682
Study Section
Special Emphasis Panel (ZRG1-NLS-3 (01))
Program Officer
Kraemer, Kristy A
Project Start
1991-01-01
Project End
2000-06-30
Budget Start
2000-01-01
Budget End
2000-06-30
Support Year
10
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Medical College of Georgia (MCG)
Department
Physiology
Type
Schools of Medicine
DUNS #
City
Augusta
State
GA
Country
United States
Zip Code
30912
Kozak, Wieslaw; Fraifeld, Vadim (2004) Non-prostaglandin eicosanoids in fever and anapyrexia. Front Biosci 9:3339-55
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Dokladny, K; Kozak, A; Wachulec, M et al. (2001) Effect of heat stress on LPS-induced febrile response in D-galactosamine-sensitized rats. Am J Physiol Regul Integr Comp Physiol 280:R338-44
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Tesfaigzi, Y; Kluger, M; Kozak, W (2001) Clinical and cellular effects of cytochrome P-450 modulators. Respir Physiol 128:79-87
Kozak, W; Kluger, M J; Tesfaigzi, J et al. (2000) Molecular mechanisms of fever and endogenous antipyresis. Ann N Y Acad Sci 917:121-34
Frank, S M; Kluger, M J; Kunkel, S L (2000) Elevated thermostatic setpoint in postoperative patients. Anesthesiology 93:1426-31
Kozak, W; Kluger, M J; Kozak, A et al. (2000) Role of cytochrome P-450 in endogenous antipyresis. Am J Physiol Regul Integr Comp Physiol 279:R455-60
Gourine, A V; Rudolph, K; Leon, L R et al. (2000) Effect of interleukin-11 on body temperature in afebrile and febrile rats. Neuroimmunomodulation 8:12-Aug
Leon, L R; Kozak, W; Rudolph, K et al. (1999) An antipyretic role for interleukin-10 in LPS fever in mice. Am J Physiol 276:R81-9

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