Mice received LPS derived from Salmonella abortus equi (L5886, Sigma, Poole, UK) at a dose of 100 μg/kg, via intra-peritoneal injection,

unless stated otherwise. This dose of LPS reduces burrowing, open-field activity, changes core body temperature and gives a reproducible cytokine response in the brain ( Teeling Tacrolimus molecular weight et al., 2007). Anti-inflammatory drugs were given 30–60 min prior to LPS injection as indicated in Table 1. Burrowing was assessed as described previously (Deacon et al., 2002, Deacon et al., 2001, Deacon, 2006 and Teeling et al., 2007). Mice received appropriate pre-treatment followed by an intra-peritoneal injection of LPS or saline. Burrowing was measured between 1 and 3 h post treatment. Open-field activity in mice was assessed using a Med Associates Activity Monitor (Med Associates Inc., Vermont). The open field consisted of an aluminium base (27 × 27 cm) enclosed

on four sides with 0.7-cm thick acrylic sheet, surrounded by an opaque screen. Each mouse was placed in the middle of Bioactive Compound Library purchase the open field and observed for 3 min. Measurement was made of total distance travelled (cm) and the total number of rears in the observation period (Felton et al., 2005). The open-field activity was measured between 3.5 and 4 h after LPS or saline injection. Body temperature was measured using a rectal probe (Physitemp, Thermalerte TH5) that gave a rapid stabilization of the measured temperature. The mice were pre-adapted to measurements of rectal temperature for two days prior to the intra-peritoneal challenges to minimise stress effects. Body temperature was measured 4.5 h after LPS or saline treatment. Mice were terminally anaesthetized and transcardially perfused with heparinised saline. Brains were rapidly removed, and a thick coronal section (2 mm) taken (at approximately −2.7 to −3.7 from Bregma). The dorsal hippocampus was then punched out from this section, rapidly frozen in liquid nitrogen and kept

at −80 °C until further use. Total RNA was extracted using RNeasy mini columns (Qiagen) according to the manufacturer’s instructions. Contaminating genomic DNA was degraded during extraction by use of DNase GNAT2 I enzyme (Qiagen). RNA samples were stored at −80 °C until assay. All equipment and reagents were supplied by Applied Biosystems Ltd. (Warrington, UK) unless stated otherwise. cDNA was generated from total RNA by the use of Taqman Gold RT reagents. The housekeeping gene glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was measured in each sample by use of a rodent GAPDH Taqman kit. Assays for IL-1β, IL-6, TNF-α, COX-2 mRNA were performed as previously described (Cunningham et al., 2005). Primers used for COX-1 measurement were as follows: forward: 5′-CCA GAA CCA GGG TGT CTG TGT-3′, reverse: 5′-GTA GCC CGT GCG AGT ACA ATC-3′, probe: FAM – CGC TTT GGC CTC GAC AAC TAC CAG TG – TAMRA.