<p>Time course of cell viability and cell death after GD was estimated by MTT and LDH assays, respectively. Bars depict rates of MTT reduction (A) and LDH release (B) time dependent manner after GD. MTT data represent relative percentages compared with controls (<i>*p<0.05</i>, <i>**p<0.001,</i> n = 3). LDH release from neuro2a cells was calculated as fold increase from the LDH release in controls (<i>*p<0.01</i>, <i>**p<0.001,</i> n = 3). (C) Levels of LC3 and p62 expression, cleaved-caspase 3 and PARP cleavage were determined at indicated times after GD by immunoblot analysis. Tubulin was used as loading control. (D) Quantitative analyses of the immunoblots are shown in (C). The amount of each protein was normalized against the amount of ...
<p>(A) Neuron-SC co-cultures showed a modest increase of apoptosis rate only at the highest glucose ...
<p><b>A</b>, Experimental design. Rat cortical neurons were exposed to 30 min non-injurious precondi...
Grown in medium with glucose and glutamine. At 0 hour the medium was replaced with fresh medium with...
<p>(A) Schematic diagram of experiment for the glucose reperfusion. Cells were incubated in glucose-...
<p>Shown is the relative LDH release of primary neuronal cells after OGD (shown as “cell death (%LDH...
<p>Data are shown for cells exposed to normal conditions (control) or glucose deprivation (vehicle) ...
<p>After 3 h GD, neuro2a cells were replaced by 20; pepstatin A (PA, 10 uM), leupeptin (Leu, 10 uM) ...
<p>After 3 h GD, neuro2a cells were replaced by 20-Methyladenine (3MA); Bafilomycin A1 (BA1) and z-V...
Neurons require a nearly constant supply of ATP. Glucose is the predominant source of brain ATP, but...
<p>DSCR1-TG neurons (white bars) exhibited an improved survival compared with WT (black bars) follow...
<p>(A) Neuronal survival was measured following prolonged incubation in indicated treatment conditio...
<p><b>A</b>, Cortical neurons isolated from CBP<sup>+/−</sup> mice or wild-type littermates were exp...
<p><b>A.</b> Dose dependent effects of METH on cell viability in human neurons at 24 hr. <b>B.</b> C...
Hypoglycemia-induced brain injury is a common and serious complication of intensive insulin therapy ...
<p><b>A</b>, Rat cortical neurons were exposed at DIV 9 (<i>in vitro</i> day 9) to oxygen-glucose de...
<p>(A) Neuron-SC co-cultures showed a modest increase of apoptosis rate only at the highest glucose ...
<p><b>A</b>, Experimental design. Rat cortical neurons were exposed to 30 min non-injurious precondi...
Grown in medium with glucose and glutamine. At 0 hour the medium was replaced with fresh medium with...
<p>(A) Schematic diagram of experiment for the glucose reperfusion. Cells were incubated in glucose-...
<p>Shown is the relative LDH release of primary neuronal cells after OGD (shown as “cell death (%LDH...
<p>Data are shown for cells exposed to normal conditions (control) or glucose deprivation (vehicle) ...
<p>After 3 h GD, neuro2a cells were replaced by 20; pepstatin A (PA, 10 uM), leupeptin (Leu, 10 uM) ...
<p>After 3 h GD, neuro2a cells were replaced by 20-Methyladenine (3MA); Bafilomycin A1 (BA1) and z-V...
Neurons require a nearly constant supply of ATP. Glucose is the predominant source of brain ATP, but...
<p>DSCR1-TG neurons (white bars) exhibited an improved survival compared with WT (black bars) follow...
<p>(A) Neuronal survival was measured following prolonged incubation in indicated treatment conditio...
<p><b>A</b>, Cortical neurons isolated from CBP<sup>+/−</sup> mice or wild-type littermates were exp...
<p><b>A.</b> Dose dependent effects of METH on cell viability in human neurons at 24 hr. <b>B.</b> C...
Hypoglycemia-induced brain injury is a common and serious complication of intensive insulin therapy ...
<p><b>A</b>, Rat cortical neurons were exposed at DIV 9 (<i>in vitro</i> day 9) to oxygen-glucose de...
<p>(A) Neuron-SC co-cultures showed a modest increase of apoptosis rate only at the highest glucose ...
<p><b>A</b>, Experimental design. Rat cortical neurons were exposed to 30 min non-injurious precondi...
Grown in medium with glucose and glutamine. At 0 hour the medium was replaced with fresh medium with...