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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Anatomy and embryology 165 (1982), S. 213-232 
    ISSN: 1432-0568
    Keywords: Callosal connections ; Neocortex ; Columnar organization ; Rat ; Degeneration techniques
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary After complete callosotomy the distribution of degeneration products was re-investigated in adult albino rats. Three to seven days post operation, coronal, horizontal and “flattened” sections were impregnated according to the new methods of Gallyas et al. (1980) which stain degenerating axons and terminals, respectively. The regional distribution patterns of callosal terminals were directly visualized with dark field illumination at low magnification. With this technique the distribution pattern of axons and terminals could be compared between different cortical regions and individuals. Callosal terminals tend to accumulate in patches or bands along the borders of cortical regions and areas. The concentration of callosal terminals was especially high at the common corners of more than two cortical areas. The callosal system shows a rather constant distribution pattern which is composed of column shaped subunits. Considerable individual variations were recognized concerning the number, position, shape, density and contiguity of the columnar units either occupied by callosal connections or empty. Although the laminar distribution of callosal terminals shows some similarities in different areas of the cortex, there is no common laminar pattern characteristic either for the whole neocortex or for any cortical region. The comparison between consecutive sections stained either for degenerating fibers or degenerating axon terminals revealed that the callosal axons do not determine directly the arrangement and packing density of callosal synapses. Whatever determines the position and amount of callosal synapses this influence seems to be exerted via translation into the columnar organization.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 47 (1979), S. 123-130 
    ISSN: 1432-0533
    Keywords: Rat ; Protein deprivation ; Neocortex ; Vessels ; Morphometry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The postnatal vascular growth in the neocortical area 18 of normal and pre- and postnatally protein-deprived rats was examined. For control rats the specific length, the specific surface and the volume fraction of vessels increased rapidly between 7 and 20 days of age. Thereafter, only a minor increase was seen. In protein-deprived rats there was no increase in the specific length of vessels between 7 and 10 days of age and this variable was still reduced at 30 days of age compared to controls. This reduction was due to a decrease in the specific length of thin vessels (Ø〈8.25 μ) whereas the specific length of wider vessels was not affected by the protein deprivation. There were no significant differences in the specific surface or volume fraction of vessels between control and protein-deprived rats. These findings indicate an adaptive increase in luminal diameter of vessels in the protein deprived rats during postnatal development. At 90 days of age no significant differences between vascular variables of control and protein-deprived rats were seen.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 19 (1971), S. 249-264 
    ISSN: 1432-0533
    Keywords: Brain Edema ; Stab Wound ; Neocortex ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The parietal cortex of rats was examined by light and electron microscopy 1–120 min after a standardized stab wound (250×450×1800μm, constant stab velocity). The changes in the tissue are already visible qualitatively after 1 min. After about 4 min the expansion of tissue changes stops. 4 zones may be separated. Surrounding the stab canal concentrically they are relatively sharply defined. Zone I. Stab canal, haemorrhagical or “debris zone”, primary traumatic destroyed zone. The tissue units are here completely destroyed. Zone II. “Squashed” or “indirectly but irreversibly damaged” zone. It is ca. 80μm wide and contains apart from a protein-rich extracellular fluid almost exclusively swollen cells and cell fragments. Zone III. Swelling brain or “intracellular peritraumatic edema”. It is ca. 150μm wide and contains mainly dark neurones and swollen astroglia. Zone IV. Transitional zone of variable width. Here only the perivascular and perineural processes are swollen without changed neurone structure. In all swollen astrocytes mitochondria are altered typically (denser matrix, dilated cristae). Discussed are: The short latency period, Zone IV, causes of astroglial swelling, origin of extracellular fluid as well as mechanisms which limit the spread of extracellular fluid into Zone II.
    Type of Medium: Electronic Resource
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