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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Neurophysiology 29 (1997), S. 205-212 
    ISSN: 1573-9007
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Various electrical, mechanical, and chemical stimuli, including the influences of neurotrasmitters, neuromodulators, and hormones, trigger complex changes in [Ca2+] i in all types of glial cells. Glial [Ca2+] i responses are controlled by coordinated activity of several molecular cascades. The initiation of [Ca2+] i signal in glial cells results from activation of either plasmalemmal, or intracellular Ca2+ permeable channels. The interplay of different molecular cascades enables the development of agonist-specific patterns of Ca2+ responses. Such agonist specificity may provide the means for intracellular and intercellular information coding. Furthermore, glial [Ca2+] i signals can travel with no decrement within glial networks. These intercellular Ca2+ waves can be regarded as a substrate for information exchange between the glial cells. Neuronal activity can trigger [Ca2+] i signals in neighboring glial cells and, moreover, there is some evidence that glial [Ca2+] i waves can activate neuronal electrical and/or [Ca2+] i , responses. Glial Ca2+ signalling can be regarded as a form of glial excitability.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Neurophysiology 29 (1997), S. 28-31 
    ISSN: 1573-9007
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Expression of functional type 1 metabotropic glutamate receptors (mGluR1) was studied in Purkinje neurons in cerebellar slices of mice. Extracellular application of 100 μM of a specific activator of G protein-coupled mGluR, (1S, 3R)-ACPD, triggered a transient elevation of [Ca2+]i in Purkinje neurons. The amplitudes of [Ca2+]i transients in the dendrites of Purkinje neurons were considerably higher than those in the somata, whereas the amplitudes of glutamate-triggered [Ca2+]i transients were similar in these cellular compartments. This suggests the preferential localization of mGluR and/or InsP3-sensitive Ca2+ stores in the dendrites of Purkinje neurons. By applying a single-cell reverse-transcriptase polymerase chain reaction (RT-PCR) technique, we also demonstrated that mRNA, responsible for the expression of mGluR1 type of glutamate receptors, is transcribed in Purkinje neurons; these receptors are likely to be responsible for (1S,3R)-ACPD-evoked calcium signalling.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-9007
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-2013
    Keywords: Intracellular calcium Intracellular pH Microglia NH3/NH4+
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract. Microglial cells are thought to serve as sensors for pathologic events in the brain. In the present study we demonstrate that these cells respond with an increase in intracellular calcium concentration ([Ca2+]i) to intracellular alkaline shifts induced by either application of NH3/NH4 + or by an extracellular alkaline shift. The cytoplasmic pH (pHi) and [Ca2+]i in cultured mouse microglial cells were studied employing the fluorescent probes BCECF and fura-2, respectively. Application of NH3/NH4 + caused an initial rapid alkalinization followed by a slow recovery towards the resting level, while application of alkaline (pH 8.2) solution triggered a slower rise in pHi. The [Ca2+]i elevation triggered by NH3/NH4 + and extracellular alkaline shift were caused by different mechanisms: extracellular alkalinization induced a transmembrane Ca2+ entry, whereas NH3/NH4 + triggered Ca2+ release from thapsigargin- and ATP-sensitive intracellular pools. The mobilization of intracellular Ca2+ caused by NH3/NH4 + was blocked by a specific inhibitor of phospholipase C, U-73122, but was not affected by an inhibitor of G-protein, pertussis toxin. This implies that NH3/NH4 interacts with phospholipase C and leads to an increase in the intracellular level of inositol 1,4,5-trisphosphate (InsP 3). In contrast to a previous study using a microglial cell line, application of NH3/NH4 + did not result in a release of tumor necrosis factor α (TNF-α), a marker of microglial activation, in the primary microglial cells. This implies that ammonium does not lead to activation of microglia in the culture model.
    Type of Medium: Electronic Resource
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