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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 116 (1997), S. 367-374 
    ISSN: 1432-1106
    Keywords: Key words Binaural bands ; Wheat germ agglutinin-horseradish peroxidase ; Cortical columns ; Auditory system ; Corpus callosum ; Ferret
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  The callosal connections of ferret auditory cortex were studied by making multiple injections of wheat germ agglutinin-horseradish peroxidase into the middle ectosylvian gyrus or by packing crystals of horseradish peroxidase into the transected corpus callosum. The primary area (AI) had strong callosal connections that arose from somata mainly located in layer III. Other layers contained sparsely distributed cells that projected across the midline. The projecting cells occurred over the whole extent of AI but were not homogeneously distributed in layer III. The axons from these cells terminated mainly in the upper layers of the contralateral cortex, where they converged onto three discrete bands. The three elongated bands lay in a dorsoventral orientation, parallel to the tonotopic axis. They were slightly curved and had a fairly uniform width. The posterior band had a width of about 200 μm, while the anterior and middle bands were more variable and had widths of 300–800 μm. The centre-to-centre distance between the posterior and middle bands was 520 ± 60 μm and for the anterior to middle bands was 620 ± 210 μm. The retrograde labelling produced by the same injections showed that the cell bodies had a higher density in the terminal bands than in the intervening spaces. The bands of dense callosal connections appear to correspond to the binaural summation columns, which have been clearly demonstrated in the ferret, but direct evidence of this will need to be sought in a future study. The discrete nature of the callosal bands in the ferret appears to make it a suitable species for studying the relationship between callosal terminals and those arising in other areas of the brain and for clarifying the possible existence of separate functional systems within the auditory cortex.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 62 (1986), S. 241-249 
    ISSN: 1432-1106
    Keywords: Superior colliculus ; Phosphorylase ; Cytochrome oxidase ; Acetylcholinesterase ; Mouse histochemistry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Patches of high phosphorylase activity are found in the intermediate and dorsal deep grey layers of the mouse superior colliculus when either coronal or sagittal sections are cut. These patches indicate that the phosphorylase a activity is arranged in a continuous lattice composed of bands of high phosphorylase a activity with a width of 100–200 μm that surround pale islands of low activity. This lattice was demonstrated by cutting surface parallel sections through the partially flattened superior colliculus. An almost identical lattice is observed in sections incubated to demonstrate total phosphorylase or cytochrome oxidase (CYO) activity. This phosphorylase/ CYO lattice extends over the entire area of the superior colliculus. A discontinuous staining pattern is also observed in the intermediate and deep grey layers of both sagittal and coronal sections incubated for acetylcholinesterase (AChE) activity. The staining is arranged in two discontinuous sheets of intense activity that are joined together by vertical streamers. In surface parallel sections the AChE activity is found to form a network pattern which extends over the entire extent of the superior colliculus but which becomes fainter at the anterior pole. The phosphorylase/CYO lattice is not in register with the AChE lattice and the two seem to be organized independently of each other despite occurring at the same depth.
    Type of Medium: Electronic Resource
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