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. 2012 Feb 23;73(4-2):814–828. doi: 10.1016/j.neuron.2011.12.026

Figure 6.

Figure 6

Activation of Infragranular Layers Mediates SHs in L2/3Ps of V1

(A) Photostimulation (PS) of L5Ps hyperpolarized overlying L2/3Ps in V1 (grand-average ± SEM; n = 5).

(B) Diagram showing the mean onset latencies ± SEM of (1) hyperpolarizations of V1 L2/3Ps driven by A1 photostimulation, (2) SHs of L2/3Ps in V1, (3) sound-driven activation of L5Ps in V1 (left) and hyperpolarizations of L2/3Ps in V1 driven by the phostimulation of L5Ps in V1 (right).

(C) Top: whole-cell recordings from L2/3Ps after the injection of muscimol in infragranular layers of V1. Bottom: Nissl-counterstained, coronal section through V1 showing that the injected fluorescent muscimol did not leak into supragranular layers. Bar, 400 μm.

(D) Muscimol abolished spiking in L5 (gray) without modifying the resting Vm of L2/3Ps (black) and its variance over time (“L5/6” in bottom plots). On the contrary, muscimol diffusion to the entire cortex dramatically affected the resting Vm and its variance (“Cortex” in bottom plots, ∗∗∗p < 0.001 for post hoc test).

(E) Acute inactivation of L5/6 activity by a local puff of muscimol counteracted SHs in overlying L2/3Ps of V1 (red, n = 16) with respect to controls (black, n = 19; ∗∗∗p < 0.01). Squares in the box plot (right) indicate the experiments with fluorescent muscimol.

See also Figure S6.