A separate cohort of animals (n = 10) received an acute IC administration of 3.2 μg CZP or 0.05 N HCl, followed 10 min later by an acute IC administration of 32, 100, or 180 μg Δ9-THC or VEH. Well-trained rats were then tested in the

radial maze task after a 5-min interval (pre-delay task) and after 1 h (post-delay task). So, drugs were injected in well-trained rats before any testing in the maze on a test day. The sequence of drug combinations for each animal MG-132 solubility dmso was determined by a Latin Square schedule, which ensured that no animal repeated a given sequence of injections. A period of 7 days with no drug treatment was interposed between drug administrations, and a training session demonstrating stable responding was required prior to each drug administration. After all experimental 20s Proteasome activity procedures, animals were lightly anesthetized with chloral hydrate (400 mg/kg, i.p.), and 0.5 μl (the same volume of drug administered) of a 1% methylene blue solution (Biotec, PR, Brazil) was administered IC. Afterwards, the rats were deeply anesthetized and intracardially perfused with saline followed by 4% formaldehyde. Brains were removed and maintained in 8% formaldehyde for at least 3 days. Then the brains were serially sectioned with a vibratome into slices of approximately 80 μm (Vibratome Tissue Section System, 1000 Plus, MO, USA).

These slices were stained with neutral red and if cannula had been properly placed, a blue dye would be seen in the mPFC (Cg1, Cg2, Cg3 and Fr2 areas), as identified in diagrams from

a rat brain atlas (Paxinos and Watson, 1986). The number of errors and the time spent in each arm in the pre- or post-delay periods of 1-h delay tasks were expressed as the means ± SEM. Drug interactions (within Δ9-THC doses and Tolmetin between antagonist effects) were analyzed using two-way repeated-measures ANOVA followed by Dunn’s (Bonferroni) correction as a post-hoc test for each pair of different groups being compared. A p-value of 0.05 or less was considered as indicative of a significant difference. The software GB-Stat Professional Statistics and either Graphics version 6.5 or GraphPad Prism 4.0 were employed for statistical analysis and graphic representation, respectively. We thank FINEP for a funding allowing us to acquire the SCH 23390 and Clozapine. The cannabinoid used in this study was provided through the courtesy of the National Institute on Drug Abuse (NIDA) and the National Institute of Mental Health (NIMH). “
“Pristanic acid (Prist) (2,6,10,14-tetramethylpentadecanoic acid), a branched-chain fatty acid derived from peroxisomal α-oxidation of phytanic acid, accumulates in various inherited peroxisomal disorders (Wanders et al., 2001). These disorders can be due to a single-protein defect or by peroxisome biogenesis disorders.