It has been shown that systemic injection of LPS quite rapidly enhances the expression of

mRNA for IL-1β, IL-6 and TNF-α in the mouse hypothalamus (Goujon et al., 1996 and Pitossi et al., 1997). Considering that IL-1β can facilitate the release of SP from neurons (Morioka et al., 2002), we investigated whether IL-1β-induced fever was mediated via SP production. However, SR140333B, at a dose that reduces 85% of the LPS-induced fever, did not alter the fever induced by IL-1β injected i.c.v, suggesting that this cytokine does not cause fever via SP release in the brain. Another possibility that should be considered is that SP, once released after LPS injection, induces the release of IL-1β which in turn causes fever. Although to our knowledge there Selleck BMN673 is no evidence

that LPS can directly bring about the release of SP in the CNS, there is evidence supporting the possibility that SP acts on astrocytes to release IL-1β (Martin CHIR-99021 mouse et al., 1992). That would explain the effectiveness of SR140333B against LPS-induced fever and not in that induced by IL-1β; however, this hypothesis needs further investigation. IL-1β induces fever by a prostaglandin-dependent pathway since it has been shown that the non-steroidal anti-inflammatory drug indomethacin inhibits the febrile response to this cytokine (Hashimoto, 1991). In addition, it has been shown that mice deficient in microsomal prostaglandin E synthase-1, the final PGE2 synthesizing enzyme, do not develop fever after IL-1β peripheral injection (Saha et al., 2005), although the expression of this and other pyrogenic cytokines is increased in the brain of these animals (Nilsberth et al., 2009b). However, the febrile response is the result of a complex interplay between various cytokines and particularly the fever induced by LPS in rats is believed to involve prostaglandin-dependent

and -independent mechanisms (Fabricio et al., 2006, Nilsberth et al., 2009a and Strijbos et al., Phosphatidylinositol diacylglycerol-lyase 1992). Since SP does not appear to mediate the IL-1β (and, therefore, prostaglandin-dependent) febrile response we decided to test the possible involvement of SP in the febrile response induced by CCL3/MIP-1α. Although it has been recently shown that CCL3/MIP-1α is not involved in LPS-induced fever (Soares et al., 2009), this cytokine does induce fever by a prostaglandin-independent pathway (Melo Soares et al., 2006). Nevertheless, in the present study the NK1R antagonist was not effective even in the prostaglandin-independent fever generated by CCL-3/MIP-1α. We mentioned before that different central mediators are involved in different pathways for fever induction. We have shown that endogenous opioids are not involved in the febrile response induced by IL-1β (Fraga et al., 2008).