Central mediators involved in the febrile response induced by polyinosinic-polycytidylic acid: Lack of involvement of endothelins and substance P

被引:13
作者
Bastos-Pereira, A. L. [1 ]
Leite, M. C. G. [1 ]
Fraga, D. [1 ]
Zampronio, A. R. [1 ]
机构
[1] Univ Fed Parana, Dept Pharmacol, BR-81540970 Curitiba, PR, Brazil
关键词
Poly I:C; Cytokine; Prostaglandin; Endothelin; Opioids; Substance P; DOUBLE-STRANDED-RNA; ACUTE-PHASE RESPONSE; TOLL-LIKE RECEPTOR-3; MESSENGER-RNA; RAT-BRAIN; BODY-TEMPERATURE; PROINFLAMMATORY CYTOKINE; TISSUE INFLAMMATION; SYSTEMIC CHALLENGE; PROSTAGLANDIN E-2;
D O I
10.1016/j.jneuroim.2014.12.011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The present study evaluated the involvement of interleukin(IL)-1 beta, tumor necrosis factor-alpha (TNF-alpha), IL-6, interferon(IFN)-gamma, prostaglandins of the E-2 series, endothelins, substance P and opioids within the central nervous system in polyinosinic:polycytidylic acid (Poly I:C)-induced fever in rats. Poly I:C injection induced a febrile response which was reduced by intracerebroventricular administration of the antibodies against TNF-alpha, IL-6, or IFN-gamma, or by IL-1 or mu receptor antagonists. Intraperitoneal injection of indomethacin or oral administration of celecoxib also reduced Poly I:C-induced fever. Poly I:C increased prostaglandin E-2 levels in the cerebrospinal fluid of the animals which was also reduced by indomethacin. The intracerebroventricular injection of ETB or NK1 receptor antagonists did not alter Poly I:C-induced fever. These data suggest the involvement of IL-1 beta, TNF-alpha, IL-6, IFN-gamma, prostaglandin E-2, and opioids but not endothelins and substance P on Poly I:C-induced fever. (C) 2014 Published by Elsevier B.V.
引用
收藏
页码:100 / 107
页数:8
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