Structural changes of auricular cartilage associated with morphological age changes of elastic fibers may be one of the causes of expansion of the auricle after reaching adulthood.

No abstract

The organization of the prefrontocaudate connection in the macaque monkey was studied with a polyacrylamide gel of horseradish peroxidase that was injected, after callosotomy, into the head of the caudate nucleus. Tissues were processed for peroxidase activity with tetramethylbenzidine. Retrogradely labeled cells appeared bilaterally in the prefrontal cortex, and ipsilaterally in the premotor area, frontal operculum, insula, and rostral region of the temporal cortex. In the prefrontal cortex, labeled cells were located in cortical layers 2-6. In layer 2, labeled cells were occasionally seen. In layer 3, a considerable number of labeled cells were seen and were mainly distributed in its lower part. They were pyramidal cells. Layer 4 contained a considerable number of labeled cells that were pyramidal or round. Somal sizes of these labeled cells were from 5 to 15 micron, but none of the cells less than 5 micron were labeled. Layer 5 was densely packed with labeled cells, though at a higher density in its upper part (5a). They were pyramidal cells. In layer 6, pyramidal or fusiform cells were labeled at a lower density than in layer 5. The laminar pattern and density of labeled cells were different among various regions of the prefrontal cortex, but, in general, the supragranular labeling tended to frequently occur in the regions containing the numerous labeled cells. There was a topographical relationship between the prefrontal regions containing the majority of labeled cells and the injection sites in the head of the caudate nucleus: the medial orbitofrontal cortex and the medial surface extending downward from the rostral sulcus project ipsilaterally to the medialmost portion of the ventromedial part of the head of the nucleus, the lateral orbitofrontal cortex projects to the ventromedial part of the head of the nucleus, and the dorsolateral prefrontal cortex ventral to the principal sulcus projects to the central part of the head of the nucleus. Our findings in the macaque monkey indicate that the corticocaudate connection is similar in laminar organization of efferent neurons to the corticocortical connections.

The corticocortical connections between the arcuate area (Walker's areas 8A and 45 or Brodmann's area 8) and the premotor and supplementary motor areas (Vogts' area 6) in the brain of the macaque monkey were studied microscopically with wheat germ agglutinin-conjugated horseradish peroxidase (WGA-HRP), which was injected into Brodmann's area 8 primarily to elucidate the projections of area 8 into area 6. In addition, in the same material, the pattern of connections between the arcuate area and area 46 of the prefrontal cortex was studied. On the basis of the findings of the present study, an anatomical cortical hierarchy for areas 8, 6, and 46 is discussed. Anterogradely labeled axon terminals and retrogradely labeled cells appeared in the premotor area, in the supplementary motor area, and in area 46 on the side of injection; sites containing labeled axon terminals also contained labeled cells. In other words, the examined connections were reciprocal. In the labeled areas, labeled terminals and cells coexisted, and most formed radial columns. However, no labeling of cells and terminals was seen in the motor area (Brodmann's area 4). After injection of WGA-HRP into area 8A, labeled terminals and cells appeared predominantly in the superior premotor area (a region of the premotor area above the arcuate spur, Vogt and Vogt's upper areas 6a alpha and 6a beta), forming one, two, or three bands of label in the anteroposterior direction, whereas labeling occurred to a lesser extent in the inferior premotor area (a region of the premotor area below the arcuate spur, Vogt and Vogt's areas 4c, lower 6a alpha and 6b). In contrast, injection of WGA-HRP into area 45 resulted in the predominant labeling of the inferior premotor area with scant labeling in the superior premotor area. In the premotor area, labeled terminals were distributed over the entire cortical depth, although few were found in the lower half of layer III, and labeled cells were distributed mainly in layer III. In area 46 of the banks of the principal sulcus in the prefrontal cortex, labeled terminals were distributed in all cortical layers or over the entire cortical depth with a lower concentration in layer IV; labeled cells were found mostly in layers III and V, with a relatively high density in layer V.

A study was made of the cytoarchitecture of the lateral and medial frontal cortex in the hamadryas baboon (Papio hamadryas). The frontal cortico-cortical connections of areas 46, 8, 6, and 4 were investigated by injection of wheat-germ agglutinine conjugated to horseradish peroxiase (WGA-HRP) into different regions of areas 46, 8, and 6. The lateral region of the frontal lobe of the baboon consists of broad areas of motor (area 4), premotor (area 6), and the dorsolateral prefrontal cortex, each of which is further divided into subdivisions with distinct cytoarchitectural features: areas 4a, 4b, 4c; 6 a alpha, 6a beta, 6a gamma, and 6b beta; 8A and 8B; 45; 46 and 46ps; 9; 10; and 12. Although the frontal cortex of the baboon brain exhibits the same basic cytoarchitectural features as the frontal corticies of the cercopithecus (campbelli?) (Vogt and Vogt, '19) or the macaque (Walker, '40; Barbas and Pandya, '87, '89), the baboon frontal cortex is very different from that of the macaque and cercopithecus in terms of cytoarchitecture: (1) the baboon frontal cortex has an additional area, termed here "6a gamma", within area 6, which has cytoarchitectural characteristics that are intermediate between those of areas 6 and 8; (2) the aggregation of giant pyramidal cells (greater than 50 microns in diameter) is found only in area 4a in the baboon, whereas such aggregates are found in areas 4a and 4b and, occasionally, in area 4c in the macaque; and (3) area 46 of the prefrontal cortex of the baboon can be subdivided into the cortex that surrounds the principal sulcus (area 46) and the upper and lower banks of the principal sulcus (area 46ps). Retrogradely WGA-HRP labeled cells and anterogradely WGA-HRP labeled terminals coexisted in the frontal cortex in a columnar fashion, indicative of a reciprocity among the connections. The frontal cortico-cortical connections of areas 46, 8, 6, and 4 in the hamadryas baboon were organized as follows: (1) areas 46, 8, and 6 were connected to one another, (2) area 4 was connected only to area 6, and (3) these connections showed a gross ventrodorsal topography: the ventral regions of each of areas 46, 8, and 6 were connected more strongly to the ventral than the dorsal regions of the other areas; the dorsal regions of each of areas 46, 8, and 6 were connected more strongly to the dorsal than the ventral regions of the other areas.(ABSTRACT TRUNCATED AT 400 WORDS)