The thalamocortical brain slice preparation allows TC input to barrel cortex to be selectively activated by extracellular stimulation in VPM and resulting synaptic responses to be monitored with extracellular or patch-clamp recordings (Agmon and Connors, 1991, Crair and Malenka, 1995 and Isaac et al., 1997). Extracellular field potential recordings were made to measure TC fEPSPs evoked by electrical

stimulation in VPM. TC inputs are glutamatergic, with the fEPSP mediated by AMPARs (Agmon and O’Dowd, 1992, Crair and Malenka, 1995, Kidd and Isaac, 1999 and Lu et al., 2001). Consistent with selleck chemicals this and previous work (Agmon and Connors, 1992 and Crair and Malenka, 1995), the fEPSP was reversibly blocked by 10 μM NBQX, an AMPAR antagonist, or a Ca2+-free extracellular solution (Figure S5). These manipulations did not block the small early downward deflection confirming that this small deflection is a presynaptic fiber volley. The strength of the TC input to layer 4 (contralateral to the intact whisker-pad) selleck products in slices prepared from sham or IO rats was compared by measuring the fEPSP: fiber volley (FV) ratio at different stimulus

intensities (Figure 5). This input/output (I/O) relationship was significantly steeper in slices from IO rats compared to sham, demonstrating an increase in TC input strength in the spared input side following IO nerve resection. There was a 47% increase in TC synaptic strength in the IO rats compared to sham. To examine whether intracortical (IC) synapses in L4 barrel cortex are strengthened following IO nerve resection, in a separate set of experiments we measured TC fEPSPs and IC fEPSPs in layer 4 (Figure S6). We confirmed the increase in the input/output relationship for TC fEPSPs but found no increase in the input/output relationship for IC fEPSPs in slices Doxorubicin from IO rats.

Thus, intracortical synaptic strength in layer 4 is not increased in spared barrel cortex in IO rats, indicating strengthening of TC synapses. The mechanism(s) underlying the increase in the TC fEPSP in the spared barrel cortex were studied with patch-clamp recordings. GABAergic feedforward inhibition in L4 barrel cortex is strongly engaged by TC afferent activity and serves to regulate coincidence detection, truncate the EPSP, and limit spike output in L4 (Chittajallu and Isaac, 2010, Cruikshank et al., 2007, Daw et al., 2007a, Gabernet et al., 2005 and Porter et al., 2001). A change in the engagement of feedforward inhibition could contribute to the change of the TC fEPSP observed in the IO rats. Whole-cell voltage-clamp recordings from L4 stellate cells were performed to measure the feedforward inhibition and feedforward excitation onto the same stellate cells using established techniques (Chittajallu and Isaac, 2010 and Daw et al., 2007a).