<p>HepG2 cells were treated with HG for 24 h. A: H<sub>2</sub>O<sub>2</sub> levels were measured using flow cytometry with DCFH-DA. B: Mitochondrial ROS level using MitoSOX red dye. Data are shown as a mean ± SEM of at least three separate experiment.: MCU knockdown cells, SC: Scramble, NG: normal glucose, HG: high glucose, # <0.05, * <0.01, * * <0.001.</p
<p>A: control group (un-treated HepG-2 cell); B: H<sub>2</sub>O<sub>2</sub> treatment group (HepG-2 ...
<p>The FI of the cell death rate was determined as the death ratio of hypoxia/normoxia. The cell dea...
Glycogen is known to act as a fuel reserve in organs such as skeletal muscle and liver. Glycogen is ...
<p>HepG2 cells were treated with HG for 24 h. After treatment, cells were lysed and protein extracts...
<p>HepG2 stable cells were generated by infecting the cells with the supernatants of lentiviruses ex...
<p>PMA (1μM) triggered the production of ROS only in dHL60 (A; C). Hyperglycemia did not affect the ...
<p>(A)(B)(D) HepG2 cells were cultured in either glucose-containing medium or glucose-deprived mediu...
<p>(A) Cells were incubated with 20 μM of 6r for the indicated times, and intracellular ROS levels w...
<p><b>(A)</b> Effects of 1 µM H<sub>2</sub>O<sub>2</sub> on ROS generation in cells exposed to 22 mM...
<p>(A) For the inhibition of XO-generated early ROS, cells were pretreated with 200 μM of allopurino...
<p>NAD, NADH, NADP and NADPH in each cell line were quantitatively determined at 24, 48 and 72 hours...
<p>HUVEC cells were treated with normal (5.5 mmol/l) or high (33.3 mmol/l) glucose in the absence or...
<p>HSCs and ISEMFs were loaded with JC-1 and exposed to plasma or to 20 µM H<sub>2</sub>O<sub>2</sub...
<p>U937 cells were lysed 2 h and 8 h after exposure to −80 mV and −46 mV Cys redox states. Cellular ...
<p>(<b>A</b>) HEK293 cells were transfected with 2 µg empty vector pRK-FLAG or 2 µg pRK-FLAG -HSCARG...
<p>A: control group (un-treated HepG-2 cell); B: H<sub>2</sub>O<sub>2</sub> treatment group (HepG-2 ...
<p>The FI of the cell death rate was determined as the death ratio of hypoxia/normoxia. The cell dea...
Glycogen is known to act as a fuel reserve in organs such as skeletal muscle and liver. Glycogen is ...
<p>HepG2 cells were treated with HG for 24 h. After treatment, cells were lysed and protein extracts...
<p>HepG2 stable cells were generated by infecting the cells with the supernatants of lentiviruses ex...
<p>PMA (1μM) triggered the production of ROS only in dHL60 (A; C). Hyperglycemia did not affect the ...
<p>(A)(B)(D) HepG2 cells were cultured in either glucose-containing medium or glucose-deprived mediu...
<p>(A) Cells were incubated with 20 μM of 6r for the indicated times, and intracellular ROS levels w...
<p><b>(A)</b> Effects of 1 µM H<sub>2</sub>O<sub>2</sub> on ROS generation in cells exposed to 22 mM...
<p>(A) For the inhibition of XO-generated early ROS, cells were pretreated with 200 μM of allopurino...
<p>NAD, NADH, NADP and NADPH in each cell line were quantitatively determined at 24, 48 and 72 hours...
<p>HUVEC cells were treated with normal (5.5 mmol/l) or high (33.3 mmol/l) glucose in the absence or...
<p>HSCs and ISEMFs were loaded with JC-1 and exposed to plasma or to 20 µM H<sub>2</sub>O<sub>2</sub...
<p>U937 cells were lysed 2 h and 8 h after exposure to −80 mV and −46 mV Cys redox states. Cellular ...
<p>(<b>A</b>) HEK293 cells were transfected with 2 µg empty vector pRK-FLAG or 2 µg pRK-FLAG -HSCARG...
<p>A: control group (un-treated HepG-2 cell); B: H<sub>2</sub>O<sub>2</sub> treatment group (HepG-2 ...
<p>The FI of the cell death rate was determined as the death ratio of hypoxia/normoxia. The cell dea...
Glycogen is known to act as a fuel reserve in organs such as skeletal muscle and liver. Glycogen is ...