Figure 1. Rapid developmental transition in M1 sensory responsiveness.
(a) The method used to record electrophysiologically from a head-fixed pup. Dots denote locations of the EMGs (forelimb, red; hindlimb, green; nuchal muscle, blue). (b) Top: Flattened cortex sectioned tangentially to the surface and stained for cytochrome oxidase (CO); primary somatosensory cortex (S1) appears darker than the surrounding tissue. Bottom: Boundaries of primary sensory areas from CO-stained tissue, illustrating S1 and primary motor cortex (M1), as well as primary auditory (A1) and visual (V1) cortex. (c) Enlargement of gray box in (b) showing the somatotopic organization within S1 and M1. hl: hindlimb. (d) Enlargement of gray box in (c) showing the locations of recording sites (blue bars) within the forelimb representation of M1. (e) Left: Representative data at P8 depicting 20 s periods of active sleep (blue) and wake (red), showing forelimb movements (twitches: blue ticks; wake movements: red ticks), unit activity within the forelimb representation of M1, and rectified EMGs from contralateral forelimb and nuchal muscles. Each row of depicts unit activity for a different neuron. The bottom-most neuron (blue or red), is represented further at right. Right, top: Raster sweeps for an individual M1 neuron triggered on twitches (blue) and wake movements (red), with each row representing a different movement. Right, bottom: Perievent histograms (bin size = 10 ms) showing the unit’s mean firing rate triggered on twitches (blue) or wake movements (red). (f) Same as in (e) except at P11. (g) Same as in (e) except at P12.