They showed that the intravenous administration of Pyr and Oxa, which decreases blood Glu levels, accelerates the brain-to-blood Glu efflux. These results support the conclusion that the brain-to-blood Glu efflux can be modulated by changes in blood Glu levels

and can be accelerated by blood Glu scavenging (Gottlieb et al., 2003). Accordingly, Zlotnik and colleagues recently tested the effects of blood Glu scavengers in a rat model of closed head injury (CHI) and observed a significant improvement of the neurological recovery in the Oxa-treated and Pyr-treated rats when compared with saline-treated controls (Zlotnik et al., 2007 and Zlotnik et al., 2008). On these bases, we hypothesized that blood Glu scavenging induced by systemic Pyr and Oxa administration SNS032 could be neuroprotective by increasing brain-to-blood

Glu efflux and thus preventing excitotoxic neuronal cell damage caused by prolonged epileptic seizures. In order to test this hypothesis, in the present Fulvestrant investigation we studied the effect of Pyr and Oxa administration in rats subjected to pilocarpine-induced SE (Cavalheiro, 1995). Pilocarpine-induced SE is a widely used model to study neurodegeneration in limbic structures after prolonged epileptic seizures, particularly the hippocampal formation (Cavalheiro et al., 1991). Male Wistar rats (weight ∼250 g) were housed in groups of five under a continuous 12 h/12 h light/dark cycle and had free access to food and water. Experimental rats were injected with 4% pilocarpine hydrochloride (350 mg/kg i.p., Merck). Scopolamine methyl nitrate (1 mg/kg s.c., Sigma) was injected 30 min before pilocarpine to reduce the peripheral cholinergic effects. Approximately 10 min after pilocarpine

injection, animals developed partial limbic seizures with secondary generalization leading to self-sustained SE (Turski et al., 1983). After five hours, SE was blocked with diazepam (10 mg/kg i.p.). A control group received saline Dichloromethane dehalogenase instead of pilocarpine (Group Saline). Based on previous experiments designed to evaluate the neuroprotective effect of pyruvate and oxaloacetate in vivo (Lee et al., 2001, Gottlieb et al., 2003, Gonzales-Falcon et al., 2003 and Zlotnik et al., 2007), pyruvate solution (250 mg/kg, i.p., pH 7.4, Alfa Aesar) (Group Pilo + Pyr), oxaloacetate solution (1.4 mg/kg, i.p., pH 7.4, Calbiochem) (Group Pilo + Oxa) or both substances (Group Pilo + Pyr + Oxa) were administrated as single injection (1.5 ml) to rats thirty minutes after the development of SE. A control group received the same volume of saline instead of pyruvate and oxaloacetate (Group Pilo + Saline). Survival rates for each experimental group were calculated.