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  • 1980-1984  (3)
  • Kainic acid  (3)
  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Cell & tissue research 216 (1981), S. 569-580 
    ISSN: 1432-0878
    Schlagwort(e): Glial response ; Chemical lesion ; Kainic acid ; Hippocampus ; Rat
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Medizin
    Notizen: Summary The cellular response of non-neuronal elements of the pyramidal cell layer of the rat hippocampus, especially the area CA 3, was observed electron microscopically following destruction of this formation by means of intraventricular administration of kainic acid (KA). The neuroglial cell types responding to the KA-induced lesion included astrocytes and the “microglia-like reactive cells”. In addition, numerous brain macrophages appeared in the damaged area CA 3. Oligodendrocytes and pericytes revealed no morphological changes. Swollen astrocytes were seen in the KA-induced lesion during the early stage. Glial filaments gradually developed in the soma and cell processes of these cells. Brain macrophages were seen in the KA-induced lesion during the early stage; they gradually decreased in number with time. Numerous small cells displaying a dark nucleus appeared in the damaged area CA 3 during the first two days after the KA-administration, and gradually increased in number. During the later stage this cell type could hardly be distinguished from the intrinsic microglial cells. It is open to discussion whether this cell type originates from the intrinsic microglial cells or from the hematogenic monocytes; therefore it is designated as “microglia-like reactive cell” in the present study.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Cell & tissue research 218 (1981), S. 75-86 
    ISSN: 1432-0878
    Schlagwort(e): Microglia ; Macrophages ; Chemical lesion ; Kainic acid ; Hippocampus ; Rat
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Medizin
    Notizen: Summary Light-and electron-microscopic investigations of kainic acid-induced lesions revealed a marked macrophage response and “microgliocytosis”. The hematogenous origin of reactive elements, such as brain macrophages and “microglia-like reactive cells”, was demonstrated when blood phagocytes were labeled with carbon particles or horseradish peroxidase prior to induction of the kainic acid-lesion. The induced lesion showed a proliferation of microglial cells, which led to a state of “microgliocytosis” in the later stage of lesioning. Since it is now generally accepted that microglial cells in the state of “microgliocytosis” are derived from the “microglia-like reactive cells”, proliferated microglial cells in the brain lesions are probably of hematogenous origin. The relationships among the brain macrophages, the “microglia-like reactive cells” and the intrinsic microglial cells are discussed.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Cell & tissue research 222 (1982), S. 223-226 
    ISSN: 1432-0878
    Schlagwort(e): Kainic acid ; Reactive microglia ; Autoradiography ; Hippocampus ; Rat
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Medizin
    Notizen: Summary Autoradiographic studies showed that in the rat hippocampus “microglia-like reactive cells” (MRC) and astrocytes are capable of proliferation in response to kainic acid (KA)-induced lesions. A marked increase in the number of labeled MRC was observed during the first four days after the induction of the KA-lesion. A proliferative response of astrocytes occurred at two days after the KA-lesion. After the induction of a KA-lesion brain macrophages and oligodendrocytes were only slightly labeled with 3H-thymidine. It appears likely that MRC is the main cellular element responding to this type of lesion.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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