<p>(A) The probe 2’,7’-dichlorohydrofluorescein (DCFH2-DA) was added to the medium of cells treated with low glucose (LG) or high glucose (HG). HG-treated cells were also treated with 100 ng/mL bFGF, 1 μM sp600125 (sp), or 1 μM U0126 (U). ROS were observed in all cells, especially in high glucose-treated cells. Bar = 100 μm. (B) Fluorescence levels in ten different cells were measured using the Image Pro Plus software. Data represent mean values ± SE of four replicates, relative to the LG group (***<i>P</i> < 0.001) and relative to the HG group (<sup>#</sup><i>P <</i> 0.05, <sup>##</sup><i>P <</i> 0.01).</p
<p>(A) Cells were pretreated with HG (30 mM glucose) for 72 hours and then incubated with bFGF (b, 1...
<p>(A) Cells were incubated with bFGF (b, 100 ng/mL), JNK inhibitor SP600125 (SP, 25 µM) or bFGF tog...
In order to investigate the mechanism of the production of oxidative DNA damage by hyperglycemia, we...
<p>Measurements performed in twenty-three subject lymphoblastoid cell lines. Reactive oxygen species...
<p>A, Reactive oxygen species (ROS) in HUVECs pre-incubated (24 hours) with D-glucose at different c...
<p>CM-H<sub>2</sub>DCFDA staining showed that high glucose concentration induced oxidative stress. O...
<p>CM-H<sub>2</sub>DCFDA indicator was used to detect ROS levels in HUVEC treated with (<b>A</b>) 5....
<p>Cells were prepared as in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0...
<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>NG, constant normal glucose (5 mM); HG, constant high glucose (22 mM); and N/HG, 5 mM alternating...
<p><b>A) Fluorescence microscopy</b> of live adherent NPCs untreated (HG) or treated with 100 µM TBH...
<p>A) carboxy-H<sub>2</sub>DCFDA (ROS, green) and C) Fim-1 diacetate (PKC, yellow) after 48 hours in...
<p>DAF-FM indicator was used to detect NO levels in HUVEC treated with (<b>A</b>) 5.6 mmol/L glucose...
<p>A and B: Observation of ROS generation by DHE fluorescent probe assay (mean ± SEM, n = 7). C: Wes...
<p>A, compared with that were treated with high mannitol (HM) and normal glucose (NG) solutions, tre...
<p>(A) Cells were pretreated with HG (30 mM glucose) for 72 hours and then incubated with bFGF (b, 1...
<p>(A) Cells were incubated with bFGF (b, 100 ng/mL), JNK inhibitor SP600125 (SP, 25 µM) or bFGF tog...
In order to investigate the mechanism of the production of oxidative DNA damage by hyperglycemia, we...
<p>Measurements performed in twenty-three subject lymphoblastoid cell lines. Reactive oxygen species...
<p>A, Reactive oxygen species (ROS) in HUVECs pre-incubated (24 hours) with D-glucose at different c...
<p>CM-H<sub>2</sub>DCFDA staining showed that high glucose concentration induced oxidative stress. O...
<p>CM-H<sub>2</sub>DCFDA indicator was used to detect ROS levels in HUVEC treated with (<b>A</b>) 5....
<p>Cells were prepared as in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0...
<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>NG, constant normal glucose (5 mM); HG, constant high glucose (22 mM); and N/HG, 5 mM alternating...
<p><b>A) Fluorescence microscopy</b> of live adherent NPCs untreated (HG) or treated with 100 µM TBH...
<p>A) carboxy-H<sub>2</sub>DCFDA (ROS, green) and C) Fim-1 diacetate (PKC, yellow) after 48 hours in...
<p>DAF-FM indicator was used to detect NO levels in HUVEC treated with (<b>A</b>) 5.6 mmol/L glucose...
<p>A and B: Observation of ROS generation by DHE fluorescent probe assay (mean ± SEM, n = 7). C: Wes...
<p>A, compared with that were treated with high mannitol (HM) and normal glucose (NG) solutions, tre...
<p>(A) Cells were pretreated with HG (30 mM glucose) for 72 hours and then incubated with bFGF (b, 1...
<p>(A) Cells were incubated with bFGF (b, 100 ng/mL), JNK inhibitor SP600125 (SP, 25 µM) or bFGF tog...
In order to investigate the mechanism of the production of oxidative DNA damage by hyperglycemia, we...