, 2002). Briefly, the reaction mixture consisted of 50 mM Tris buffer, pH 7.5,

containing 7.0 mM phosphocreatine, 7.5 mM MgSO4, and 0.5–1.0 μg protein in a final volume of 0.1 mL. The reaction was then started by addition of 4.0 mM ADP Selleck Talazoparib and stopped after 10 min by addition of 0.02 mL of 50 mM p-hydroxy-mercuribenzoic acid. The creatine formed was estimated according to the colorimetric method of Hughes (1962). The color was developed by the addition of 0.1 mL 20% α-naphtol and 0.1 mL 20% diacetyl in a final volume of 1.0 mL and read after 20 min at λ = 540 nm. Results were calculated as μmol of creatine min−1 mg protein−1. The reaction mixture for the Na+, K+-ATPase assay contained 5 mM MgCl2, 80 mM NaCl, 20 mM KCl, 40 mM Tris–HCl buffer, pH 7.4, and purified synaptic membranes (approximately 3 μg of protein) in a final volume of 200 μL. The enzymatic assay occurred at 37 °C during 5 min and started by the addition of

ATP (disodium salt, vanadium free) to a final concentration of 3 mM. The reaction was stopped by the addition of 200 μL of 10% trichloroacetic acid. Mg2+-ATPase ouabain-insensitive was assayed under the same conditions with the addition of 1 mM ouabain. Na+, K+-ATPase activity was calculated by the difference between the two assays (Tsakiris and Deliconstantinos, 1984). Released inorganic phosphate (Pi) was measured by the method of Chan et al. (1986). Enzyme-specific activities were calculated as nmol Pi released−1 min−1 mg protein. Protein was measured Selleckchem Ceritinib by the methods of Lowry et al. (1951) using bovine serum albumin as standard. Unless otherwise stated, results are presented as mean ± standard deviation.

Assays were performed in duplicate or triplicate and the mean or median was used for statistical analysis. Data was analyzed using one-way analysis of variance (ANOVA) followed by the post-hoc Duncan multiple range test when F was significant. Only significant F values are shown in Nintedanib chemical structure the text. Differences between groups were rated significant at p < 0.05. All analyses were carried out in an IBM-compatible PC computer using the Statistical Package for the Social Sciences (SPSS) software. We are grateful to the financial support of CNPq, PROPESq/UFRGS, FAPERGS, PRONEX, FINEP Rede Instituto Brasileiro de Neurociência (IBN-Net) # 01.06.0842-00 and INCT-EN. "
“Due to a publishers error the image form Fig. 11 was used for Fig. 10 in the article above. For the readers convenience the correct image for Fig. 10 is provided below. The article is correct in the online version. Fig. 10. Electron microscopic localization of ERβ-EGFP in dendrites in the PVN. (A and B) peroxidase labeling for ERβ-EGFP is found throughout the cytoplasm of large (A) and small (B) dendritic profiles. Both types of EGFP-labeled dendritic profiles, > are contacted by unlabeled terminal (uT). C.