The increase in carbonyl formation caused by Orn and Hcit was fully prevented by this pre-treatment, as shown in Fig. 2B and C (Orn: [F(3,19) = 5.114; p < 0.01]; Hcit: [F(3,18) = 8.666; p < 0.01]). GSH concentrations measured in cerebral cortex 30 min after Orn and Hcit ICV administration

revealed that Hcit moderately reduced (15%) the concentrations of GSH after Hcit injection, whereas Orn did not alter this parameter [F(2,16) = 6.608; p < 0.01] (nmol/mg protein: n = 6; control: 4.25 ± 0.45; Orn: 3.95 ± 0.17; Hcit: 3.66 ± 0.14). The next set of experiments was carried out to investigate the effect of ICV administration of Orn and Hcit on the activities of the antioxidant enzymes SOD, CAT and GPx. Fig. 3 shows that only Hcit was able to reduce the activities of GPx [F(2,17) = 3.786; Selleckchem Omipalisib p < 0.05] and CAT see more [F(2,18) = 8.328; p < 0.01], without affecting SOD activity. We also verified that Orn was not able to change any of these activities. The effect of Orn and Hcit on reactive nitrogen species generation was assessed by measuring nitrate and nitrite production. We observed that this parameter was not altered by Orn and Hcit ICV administration (nmol/mg protein: n = 5; control: 2.88 ± 1.23; Orn: 2.43 ± 0.89; Hcit: 2.15 ± 0.87). We investigated the effect of ICV injection of Orn and Hcit on CO2

production from labeled substrates in cortical homogenates. Fig. 4 shows that CO2 production from [U-14C] glucose was significantly inhibited by Orn (35%) and Hcit (32%)

[F(2,12) = 5.515; p < 0.05] 30 min after ICV treatment. CO2 formation from [1-14C] acetate was also inhibited by Orn (32%) and Hcit (25%) administration [F(2,12) = 11.048; p < 0.01]. These results suggest that the aerobic glycolytic pathway and the CAC activity were compromised by Orn and Hcit. We also evaluated the effect of Orn and Hcit ICV administration on CAC enzyme activities. We found that Etoposide concentration Hcit, significantly inhibited (20%) aconitase activity (μmol NADPH min− 1 mg protein− 1: n = 6; control: 1339.4 ± 82.9; Orn: 1208.4 ± 135.6; Hcit: 1070.4 ± 96.9), [F(2,14) = 8.450, p < 0.01], whereas Orn did not alter this activity. Furthermore, citrate synthase, isocitrate dehydrogenase, α-ketoglutarate dehydrogenase, succinate dehydrogenase, and malate dehydrogenase activities were not changed by Orn and Hcit administration (results not shown). The next set of experiments was performed to evaluate the effect of ICV injection of Orn and Hcit on the activities of the respiratory chain complexes I–III, II, II–III and IV. We found that complex I–III activity was significantly inhibited by Orn (20%) and Hcit (26%) [F(2,15) = 10.274; p < 0.01], with no significant alteration of the other tested activities of the respiratory chain ( Table 1).