, 2007). STDP can also be induced in vivo in the locust olfactory system, at synapses from Kenyon cells (KCs) onto β-lobe neurons (β-LN). Associative strengthening of KC → β-LN synapses occurs when a subthreshold KC input precedes a second, suprathreshold KC input that evokes a spike in the β-LN. Pairing single KC inputs with a suprathreshold current pulse in the β-LN induces synapse-specific, Hebbian STDP of the KC synapse, with LTP occurring for pre-leading-post spike pairings (0 < Δt < 20 ms), and LTD for post-leading-pre

pairings (−20 < Δt < 0 ms) (Cassenaer and Laurent, 2007). Thus, sensory-spike pairing evokes STDP in vivo that can be directly observed at the synapse level. STDP in vivo is often smaller, briefer and more variable compared to in vitro brain slices, and the LTP component is less prominent (Feldman, 2000; Froemke and Dan, 2002; Meliza and find protocol Dan, 2006; Jacob et al., 2007). This may reflect reduced bAP propagation in vivo, or involvement selleck kinase inhibitor of more distal synapses that show less STDP. Two different visual stimuli that are sequentially

flashed at a brief delay evoke spikes in two corresponding neuronal populations at the flashed interval (Fu et al., 2002; Yao and Dan, 2001). This may induce STDP at synapses between these populations. This was first tested in V1 of adult cats using extracellular single-unit recording. The orientation tuning of a neuron was measured, followed by a conditioning period in which a nonoptimal oriented stimulus (the “conditioned orientation”) was flashed just before (after) a preferred orientation stimulus. After 1,600–3,200 stimulus pairings, the neuron’s orientation tuning shifted toward (away) from the conditioned orientation, but only for pairing delays of <20 ms, not 42 ms (Yao and Dan, 2001; Yao et al., 2004). This temporal order and timing dependence is consistent with Vasopressin Receptor Hebbian STDP at horizontal projections between neurons tuned to the trained orientations. Similarly, repeated sequential presentation of two neighboring retinotopic stimuli

(<50 ms delay, 800–1,200 pairings) causes the spatial location of V1 receptive fields to shift toward the location activated first, consistent with Hebbian STDP at intracortical connections between nearby retinotopic loci in V1. Cross-correlation analysis confirmed that connections from early- to late-activated neurons functionally strengthen, while those in the opposite direction weaken, consistent with Hebbian STDP (Fu et al., 2002). Similar stimulus timing-dependent plasticity also occurs for frequency tuning in ferret primary auditory cortex (Dahmen et al., 2008). However, the magnitude of these plasticity effects is quite small (2° change in preferred orientation, < 2% shift in retinotopic position), and direct evidence that they represent STDP is lacking.