Microelectrode maps of somatosensory inputs were related to cortical architecture and patterns of cortical connections to provide evidence for five subdivisions of the somatosensory or sensorimotor cortex in North American opossums (Didelphis marsupialis). Microelectrode recordings revealed three systematic representations of the body surface. A large mediolaterally oriented representation was identified as the primary somatosensory area (S1) by its relative position, somatotopy, architecture, and connections. S1 represented the hindlimb, trunk, forelimb, and face in a mediolateral sequence. Two additional representations of cutaneous receptors were found caudolateral to S1, each with face representations adjacent to the border of lateral S1 and other body-part representations progressing more caudally toward the auditory cortex. We identified the more dorsal field as the second somatosensory area (S2) and the more ventral field as the parietal ventral area (PV). Tracers injected into S1 labeled neurons and terminals in architectonically distinct fields rostral and caudal to S1, the somatosensory caudal area (SC) and the somatosensory rostral area (SR). Movements could be evoked by microstimulation from sites scattered over S1, SR, and the frontal cortex, but thresholds were high and uncharacteristic of motor cortex. S2 and PV merged caudally with the cortex responsive to auditory stimuli, possibly A1, and neurons in some caudal recording sites in PV were activated by both auditory and cutaneous stimuli. Primary (V1) and secondary (V2) visual areas were also identified by microelectrode mapping, architecture, and connections. In addition, at least part of the cortex between V2 and the somatosensory cortex had visual connections. Thus, most of the dorsolateral cortex of opossums appears to be somatosensory, auditory, or visual.
Transection of a sensory nerve in adults results in profound abnormalities in sensory perception, even if the severed nerve is surgically repaired to facilitate accurate nerve regeneration. In marked contrast, fewer perceptual errors follow nerve transection and surgical repair in children. The basis for this superior recovery in children was unknown. Here we show that there is little or no topographic order in the median nerve to the hand after median nerve section and surgical repair in immature macaque monkeys. Remarkably, however, in the same animals the representation of the reinnervated hand in primary somatosensory cortex area (area 3b) is quite orderly. This indicates that there are mechanisms in the developing brain that can create cortical topography, despite disordered sensory inputs. Presumably the superior recovery of perceptual abilities after peripheral nerve transection in children depends on this restoration of somatotopy in the central sensory maps.
To characterize the postnatal development of geniculocortical axon arbor morphology in owl monkeys at a series of ages from birth to adulthood, individual arbors were bulk-filled with HRP in brain slice preparations and were reconstructed from serial sections. At all ages, cortical layers and sublayers were obvious. Presumed M or magnocellular arbors were largely confined to layer IVa, but they also extended into layer IIIc (IVB of Brodmann, 1909); presumed P or parvocellular arbors were almost exclusively confined to layer IV/3. Other axons that may reflect feedback projections from MT terminated in layer IIIc. Overall, M axon arbors increased in size and complexity from birth to adulthood with mean surface-view arbor areas ranging from 0.08 ± 0.01 mm 2 in newborns to 0.24 ± 0.02 mm 2 in adults. The developing P arbor areas were, on average, as large or larger than adult (newborn = 0.07 ± 0.01 mm 2 , adult = 0.047 ± 0.01 mm 2 ; n.s.) but the arbors were somewhat less complex. Since the brain and area 17 increase in size postnatally, the proportion of area 17 subserved by each P arbor would decrease in postnatal development. Terminal boutons with immature features were evident in both M and P populations at all developmental ages. The results indicate that, while both LGN axon types in monkeys undergo morphological changes postnatally, M arbors appear to mature by increasing arbor size and terminal branching complexity, whereas P arbors increase in complexity but not in size. These distinct programs of axon arbor development suggest that the periods of susceptibility of geniculocortical axon arbors to postnatal influences of the environment, and the types of plastic responses they potentially exhibit, are class-specific.
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