All animal use followed NIH guidelines and was in compliance with the University of Michigan Committee on Use and Care of Animals. Dissociated postnatal (P0-2) rat hippocampal neuron cultures were prepared as previously described (Sutton et al.,

2006). mEPSCs were recorded from a holding potential of – 70 mV with an Axopatch 200B amplifier from neurons bathed in HEPES-buffered saline (HBS) containing: 119 mM NaCl, 5 mM KCl, 2 mM CaCl2, 2 mM MgCl2, 30 mM Glucose, 10 mM HEPES (pH 7.4) plus 1 μM TTX and 10 μM bicuculine; mEPSCs were analyzed with Synaptosoft minianalysis Olaparib software. For paired-pulse facilitation experiments, evoked EPSCs were elicited Selleck Androgen Receptor Antagonist with 0.3 ms pulses

delivered by an extracellular bipolar stimulating electrode positioned near the recorded neuron. All PPF experiments were conducted in HBS with 0.5 CaCl2 and 3.5 MgCl2 within 15 min of CNQX or CNQX/TTX washout. Whole-cell pipette internal solutions contained: 100 mM cesium gluconate, 0.2 mM EGTA, 5 mM MgCl2, 2 mM ATP, 0.3 mM GTP, 40 mM HEPES (pH 7.2). Statistical differences between experimental conditions were determined by ANOVA and post-hoc Fisher’s LSD test. U6 promotor-driven scrambled and BDNF shRNA-expressing plasmids were obtained from OriGene Technologies (Rockville, MD); BDNF shRNA 1: 5′-TGTTCCACCAGGTGAGAAGAGTGATGACC-3, BDNF shRNA 2: 5′-GTGATGCTCAGCAGTCAAGTGCCTTTGGA-3′, scrambled: 5′-GCACTACCAGAGCTAACTCAGATAGTACT-3′. Each plasmid additionally contains a tRFP expression cassette driven by a

distinct (pCMV) promoter. Neurons were transfected with 0.5 μg of total DNA with the CalPhos Transfection kit (ClonTech; Mountain View, CA) according to the manufacturer’s protocol. All experiments were performed 24 hr after transfection. Samples were collected in lysis buffer containing 100 mM NaCl, 10 mM NaPO4, 10 mM Na4P2O7, 10 mM lysine, 5 mM EDTA, 5 mM EGTA, 50 mM NaF, 1 mM NaVO3, 1% Triton-X, 0.1% SDS, and 1 tablet Complete Mini protease inhibitor cocktail (Roche)/7 ml, pH 7.4. Equal amounts of protein for each sample were loaded and separated on 12% polyacrylamide gels, then transferred to PVDF membranes. isothipendyl Blots were blocked with Tris-buffered saline containing 0.1% Triton-X (TBST) and 5% nonfat milk for 60 min at RT, and incubated with a rabbit polyclonal primary antibody against BDNF (Santa Cruz, 1: 200) for either 60 min at RT or overnight at 4°C. After washing with TBST, blots were incubated with HRP-conjugated anti-rabbit secondary antibody (1:5000; Jackson Immunoresearch); this was followed by chemiluminescent detection (ECL, Amersham Biosciences). The same blots were reprobed with a mouse monoclonal antibody against α-tubulin (1:5000, Sigma) to confirm equal loading.