2009
DOI: 10.1016/j.neures.2009.09.713
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Imaging extrasynaptic glutamate dynamics in the brain

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Cited by 39 publications
(66 citation statements)
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References 24 publications
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“…Together with the increasing colocalization of GLT‐1 and AQP4 in these areas, this supports the idea of an increased glutamate–water buffering domain that develops as a response to ischemic conditions, a duality that is not maintained in the very close vicinity of the neurons themselves. Glutamate has also been suggested to escape from the synaptic clefts, generating an extrasynaptic glutamate pool, or the so‐called glutamate spillover phenomenon . As our data suggest, it seems that this perineuronal glutamate‐diffusing compartment becomes more abundant in pathological conditions, but further analysis on nonaged or non‐injured cellular setups are needed to confirm/infirm the presence of a closer immediately perineuronal glutamate uptake compartment.…”
Section: Discussionmentioning
confidence: 70%
“…Together with the increasing colocalization of GLT‐1 and AQP4 in these areas, this supports the idea of an increased glutamate–water buffering domain that develops as a response to ischemic conditions, a duality that is not maintained in the very close vicinity of the neurons themselves. Glutamate has also been suggested to escape from the synaptic clefts, generating an extrasynaptic glutamate pool, or the so‐called glutamate spillover phenomenon . As our data suggest, it seems that this perineuronal glutamate‐diffusing compartment becomes more abundant in pathological conditions, but further analysis on nonaged or non‐injured cellular setups are needed to confirm/infirm the presence of a closer immediately perineuronal glutamate uptake compartment.…”
Section: Discussionmentioning
confidence: 70%
“…Confocal and two-photon microscopies utilize fluorescence contrast (mostly from exogenous dyes) to measure neuron morphology and distribution [63], ion concentration [64] and synaptic release [65], cerebral blood flow and angiograms [66, 67]. OCT offers a complementary method for neuroimaging.…”
Section: Oct In Brain Imagingmentioning
confidence: 99%
“…Another promising opportunity for molecular imaging of RGCs lies in the imaging of RGC dysfunction before cell death. Several imaging probe such as reactive oxygen (ROS) [118] , mitochondria selective JC-1 [119] , and E glutamate [120] hold great promise in improving the molecular imaging of RGCs. Beyond autofluorescence imaging, several RPE-related molecular targets may also warrant consideration, such as ROS [121] , β-amyloid, esterified cholesterol and carbohydrate moieties in drusen [122] .…”
Section: Molecular Imagingmentioning
confidence: 99%