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  • Articles: DFG German National Licenses  (2)
  • Indoleamine containing nerve terminals  (1)
  • Microglia  (1)
  • 1
    ISSN: 1432-0878
    Keywords: Indoleamine containing nerve terminals ; Chemically induced degeneration ; 5,6-dihydroxytryptamine ; Rat brain
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary 5,6-dihydroxytryptamine (5,6-DHT) has been found to induce a substantial degree of “chemical degeneration” of indoleamine containing nerve terminals in the rat brain following a single intraventricular injection of 75 μg 5,6-DHT per animal. The disintegration of varicose terminal portions of serotonin containing neurons is reflected 1. by a loss of yellow fluorescent varicosities in certain defined parts of the rat CNS, despite a mild inhibition of the serotonin catabolizing enzyme monoamine oxidase with nialamide in the pretreated animals, 2. by a significant drop of the chemically measurable 5-hydroxytryptamine content in nearly all parts of the rat brain and spinal cord, 3. by the appearance of highly, orange or brownish fluorescent axons provided with numerous unusually large, distorted and intensely fluorescent swellings (“droplets”), resembling proximal stumps of mechanically severed indoleamine containing axons, 4. a temporary increase in the amount of indoleamine fluorophores stored in some neuronal pericarya, and 5. the electron microscopical demonstration of degenerating synaptic swellings of unmyelinated axons at all sites investigated. The selectivity of the effect of 5,6-DHT on indoleamine neurons is indicated by the absence of similar signs of injury in catecholamine containing neurons of the rat CNS.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-0878
    Keywords: 14C-5,6-DHT-Melanin ; Phagocytotic stimulant ; Intrathecal and subependymal phagocytes ; Microglia ; Peripheral disposition
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary 14C-5,6-DHT-Melanin was injected into the left lateral ventricle of adult rats and its fate followed by light and EM autoradiography and by TEM of structures identified as labeled in preceding light micrographs. Shortly after injection, melanin particles were seen ingested by supraependymal and epiplexus cells, by cells residing in the pia-arachnoid, i.e. free subarachnoidal cells and perivascular cells, and by subependymally located microglia-like cells with intraventricular processes. Up to day four, an increase in the number of labelled phagocytes in the CSF was noted which transformed into typical reactive macrophages. After this time, many intraventricular melanin-laden phagocytes formed rounded clusters; cells of such clusters were subsequently found to invade the brain parenchyma by penetrating the ependymal lining and to accumulate in the perivascular space of brain vessels. 14C-Melanin-storing macrophages were found in the marginal sinus of the deep jugular lymph nodes suggesting emigration of CNS-derived phagocytes via lymphatics or prelymphatics that contact the subarachnoidal space compartment. This does not exclude the possibility that some of the macrophages leave the brain via the systemic circulation by penetrating the vascular endothelium; these may be disposed of in peripheral organs other than the lymph nodes. The ability of supraependymal, epiplexus, free subarachnoidal and perivascular cells in the pia and of subependymal microglia cells to accumulate synthetic melanin by phagocytosis suggests that these cells are local variants of the same type of resting potential phagocytes of the mammalian brain. The present study shows that 14C-5,6-DHT-melanin is an ideal phagocytic stimulant and marker for phagocytosis.
    Type of Medium: Electronic Resource
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