2012
DOI: 10.1016/j.neuroimage.2011.12.038
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The neurochemical profile quantified by in vivo 1H NMR spectroscopy

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Cited by 203 publications
(266 citation statements)
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References 329 publications
(453 reference statements)
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“…IP3 (Berridge, 2009;Berridge et al, 1989). Inositol and its metabolites are present in glia and neurons, including in myelin lipid membranes (Duarte et al, 2012). Increased inositol could reflect: inflammation resulting in activation of astrocytes and microglia in which inositol levels are relatively high; dysregulation of osmotic balance; and/or reduced metabolism of inositol to PIs related to deficient myelination (Duarte et al, 2012;Schmitt et al, 2015).…”
Section: Metabolic and Structural Changes In Cps Micementioning
confidence: 99%
See 1 more Smart Citation
“…IP3 (Berridge, 2009;Berridge et al, 1989). Inositol and its metabolites are present in glia and neurons, including in myelin lipid membranes (Duarte et al, 2012). Increased inositol could reflect: inflammation resulting in activation of astrocytes and microglia in which inositol levels are relatively high; dysregulation of osmotic balance; and/or reduced metabolism of inositol to PIs related to deficient myelination (Duarte et al, 2012;Schmitt et al, 2015).…”
Section: Metabolic and Structural Changes In Cps Micementioning
confidence: 99%
“…Inositol and its metabolites are present in glia and neurons, including in myelin lipid membranes (Duarte et al, 2012). Increased inositol could reflect: inflammation resulting in activation of astrocytes and microglia in which inositol levels are relatively high; dysregulation of osmotic balance; and/or reduced metabolism of inositol to PIs related to deficient myelination (Duarte et al, 2012;Schmitt et al, 2015). As noted above, CPS mice exhibit increased levels of peripheral and central inflammatory factors (Azzinnari et al, 2014;Fuertig et al, 2016) and decreased expression of oligodendrocyte-myelination genes (Azzinnari et al, 2014;Fuertig et al, 2016).…”
Section: Metabolic and Structural Changes In Cps Micementioning
confidence: 99%
“…The similarities and differences between AQSES, which was used in this study, and other quantification methods have been described by Poullet et al [11]. The extensive use of prior knowledge allows the quantification of 20 or more metabolites, at least for high magnetic field strengths and excellent B 0 homogeneity [5,[14][15][16][17][18][19]. However, even under favorable experimental conditions and if correct prior knowledge is used, the separate quantification of some metabolites is difficult.…”
Section: U N C O R R E C T E D P R O O F Introductionmentioning
confidence: 76%
“…However, a separate quantification of Cr and PCr is hampered independent of line width, even for small temperature changes from 37 °C. While the simulations were performed for 7 T, small changes of chemical shifts due to pyrexia or anaesthesia should also be taken into account at higher B 0 to avoid quantification errors, even in case of an excellent separation between the CH 2 signals of Cr and PCr [16][17][18]. Alternatively, the CH 3 and CH 2 signals of Cr and PCr could be modelled as separate singlet signals.…”
Section: Discussionmentioning
confidence: 99%
“…Pathological conditions characterized by acute failure of energy metabolism, i.e., ischemic stroke, hypoxia, and traumatic brain injury, exhibit drastic NAA attenuation from within minutes to hours following the specific initiating event. 4,5 This attenuation during the acute stage may initially involve a deterioration of NAA synthesis, acceleration of NAA catabolism, or their combination. These pathologic conditions often lead to a combination of brain tissue necrosis and neuronal loss within several days to a week following the ischemic event unless energy metabolism is resumed within the first several hours.…”
Section: Introductionmentioning
confidence: 99%