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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 17 (1971), S. 103-113 
    ISSN: 1432-0533
    Keywords: Tri-Ortho-Cresyl-Phosphate ; Spinal Ganglion ; Neurofilaments ; Electron Microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Es wurden Spinalganglien und periphere Nerven von normalen und mit Tri-Ortho-Cresyl-Phosphat (TOCP) vergifteten Hühnern elektronenmikroskopisch untersucht. In den normalen Ganglien fanden sich zwei unterschiedliche Neuronentypen, große Zellen mit hellem Cytoplasma, in dem sich reichlich Neurofilamente fande, und kleinere Neurone, welche wenig oder keine Filamente enthielten. Die “hellen” Zellen reagierten auf TOCP mit einer starken Vermehrung der Neurofilamente, während die dunklen, kleineren Neurone eine Hypertrophie des endoplasmatischen Reticulums zeigten. Diese Veränderungen waren eindeutig nach 15 tägiger TOCP-Applikation sichtbar. An den peripheren Nerven traten bereits nach 6 tägiger Vergiftung deutlichen Reaktionen im Sinne einer Proliferation der glatten Membranen auf. Die möglichen Zusammenhänge dieser Veränderungen werden diskutiert.
    Notes: Summary The spinal ganglia and peripheral nerves of normal and tri-ortho-cresyl phosphate (TOCP)-poisoned chickens were examined with the electron microscope. The normal ganglia contained two main neuron types, a large neuron with light cytoplasm and abundant neurofilaments, and a smaller, darker cell which contained few or no filaments. The “light” neurons reacted to TOCP with a very great increase in the number of filaments present in the cytoplasm, while the darker cells showed a hypertrophy of the endoplasmic reticulum. These changes were not definitely present until 15 days after TOCP ingestion, while the largediameter fibres of the peripheral nerves showed a proliferation of smooth membranes at 6 days. The possible mechanisms for these changes are discussed.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 113 (1971), S. 396-419 
    ISSN: 1432-0878
    Keywords: Lateral geniculate nucleus ; Synapses ; Interneuron ; Transneuronal degeneration ; Monkey
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Two neuron types are distinguished by electron microscopy in the lateral geniculate nucleus (LGN) of the monkey-a large cell (P cell) interpreted as a geniculostriate relay cell, and a small cell (I cell) interpreted as an inhibitory interneuron. The I cell, distinguished by its small size, infolded nucleus, small mitochondria, cilium and small granular bodies, forms about 10% of the total neuron population. It could not be determined whether this cell has an axon, but its dendrites, which contain aggregates of flattened vesicles, are thought to form a proportion of the “F processes”, profiles which are post-synaptic to the retinal (RLP) axons and presynaptic to the dendrites of the P cells. The small dark (RSD) axon terminals of unknown origin contact the dendrites of both cell types. After eye enucleation the P cells of the affected laminae of the LGN shrink and partially withdraw their dendrites from the neuropil. By 29 months' survival, they have only a narrow cytoplasmic rim around the nucleus. A necrotic process also occurs, affecting fine dendrites by 22 days and large profiles by 45 days, but it is not clear whether whole cells are destroyed by this process. At 45 days the I cells are commonly seen to form somatodendritic synapses. The appearance of these synapses is interpreted as the result of a withdrawal to the soma of the presynaptic dendrites. It is concluded that the I cells are probably inhibitory interneurons subject to excitation and presynaptic inhibition by the RLP and RSD axons, and a diagram is presented to demonstrate the possible significance of these connections for the transmission of information through the LGN.
    Type of Medium: Electronic Resource
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