The functional status and columnar organization of single cells responding to cutaneous stimulation in neonatal rat somatosensory cortex S1.

1. An investigation was carried out on single cells in 7 day old rat primary somatosensory cortex, which responded to cutaneous stimulation using mechanical pulses. 3 percent of cells encountered showed stable spontaneous activity, whereas 88 percent were silent in the absence of intentional stimulation. The remainder showed unstable spontaneous activity. In contrast, the great majority of adult cells were spontaneously active in the absence of stimulation, under similar conditions of urethane anaesthesia. 2. The distribution within cortical layers of cutaneously driven cells was similar in adult and 7 day old rats, and similar to that found in adult mammalian cortex by other workers. 3. 7 day old cells showed diminished excitability to cutaneous stimulation with stimuli at intervals below 10-15 sec, whereas adult cells could be successfully repetitively driven with stimuli at intervals of 500 msec. The low ability of the immature cells to follow repetitive cutaneous stimulation is not due to an overall depression of these cells excitability per se. Latencies of unitary responses in these immature cells were about sixfold those found in equivalent cells at maturity. 4. Columnar organization at seven days of age was similar in outline to that of the adult, but much less discrete. Receptive fields were considerably larger at 7 days and evidence is given that this may be due to inadequate surround inhibition. Immature vibrissae-driven units were directionally selective. 5. At 7 days of age, long inter-spike intervals were rare in spontaneously active cells with the result that inter-spike interval histogram distributions (i.h.s.) were approximately normal. Corresponding i.h.s. of adult cells invariably showed skew distributions. 6. Tactile stimulation of centre receptive fields produced an increase in short and long intervals from spontaneously active cells at each age. In contrast to adult cells, the immature cells commonly responded cyclically, with alternating phases of increased and decreased firing rate for periods of up to 3 sec following punctate stimulation. 7. Decrease in spontaneous firing rate, following the first phase of excitation, was profound in 7 day old cells, and implied that inhibitory mechanisms operate at an early age in the rat somatosensory system. These mechanisms also appear to contribute to cyclical activity of 7 day old cells when driven by punctate cutaneous stimulation.