<p>(A) Real-time PCR analysis was performed to measure Insulin1 and Insulin2 mRNA 24 h after treatment with 10% GS. Relative quantification was used to calculate the change in insulin mRNA, which was depicted as the fold change. (B) INS-1 cells transfected with pGL3-insulin constructs for 24 h, followed by treatment with nonglycated (NG) or 10% GS for a further 24 h. Lysates were harvested for the luciferase assay. (C) INS-1 cells cultured with NG or 10% GS for 24 h. Insulin content was measured after acidified ethanol extraction. Data are represented of three separate experiments. **p<0.01 vs. NG.</p
The purpose of the present study was to evaluate the direct effects of advanced glycation end produc...
<p>(<b>A</b>) The indicated cells were preincubated with the PI-3 kinase inhibitor LY294002 for 1 ho...
<p>(A) INS-1 cells were pretreated with RAGE antibody for 1 h and then treated with nonglycated (NG)...
<p>INS-1 cells were treated with NG, 1% GS, 2% GS, 5% GS or 10% GS for 1, 3, 6 and 12 h, and then <i...
We investigated 1) the ability of purified glargine (GLA), metabolites 1 (M1) and 2 (M2), IGF-I, and...
We investigated 1) the ability of purified glargine (GLA), metab-olites 1 (M1) and 2 (M2), IGF-I, an...
<p>(<b>A</b>) Primary rat and human hepatocytes (n = 3) were treated with 2-AG-ether in the absence ...
International audienceParenteral-nutrition (PN)-induced hyperglycemia increases morbidity and mortal...
<p>Seventy two hours post transfection cells were stimulated with 3 mM or 25 mM glucose, supplemente...
<p>Insulin degradation products were qualitatively measured after incubation with (A) partially-puri...
<p>(A) INS-1 cells were treated with nonglycated (NG; control) serum or with varying concentrations ...
<p>Insulin released into culture medium from day 0 to 3 and from day 12 to 15 and also in extracts c...
<p>(A, C-F) INS-1E cells and (B) isolated mouse islets were cultured in the presence of test substan...
<p>(A–D) INS-1 cells were cultured for 14 days. (E and F) under normal-culture-glucose (11.2 mmol/l;...
The presence and biological significance of circulating glycated insulin has been evaluated by high-...
The purpose of the present study was to evaluate the direct effects of advanced glycation end produc...
<p>(<b>A</b>) The indicated cells were preincubated with the PI-3 kinase inhibitor LY294002 for 1 ho...
<p>(A) INS-1 cells were pretreated with RAGE antibody for 1 h and then treated with nonglycated (NG)...
<p>INS-1 cells were treated with NG, 1% GS, 2% GS, 5% GS or 10% GS for 1, 3, 6 and 12 h, and then <i...
We investigated 1) the ability of purified glargine (GLA), metabolites 1 (M1) and 2 (M2), IGF-I, and...
We investigated 1) the ability of purified glargine (GLA), metab-olites 1 (M1) and 2 (M2), IGF-I, an...
<p>(<b>A</b>) Primary rat and human hepatocytes (n = 3) were treated with 2-AG-ether in the absence ...
International audienceParenteral-nutrition (PN)-induced hyperglycemia increases morbidity and mortal...
<p>Seventy two hours post transfection cells were stimulated with 3 mM or 25 mM glucose, supplemente...
<p>Insulin degradation products were qualitatively measured after incubation with (A) partially-puri...
<p>(A) INS-1 cells were treated with nonglycated (NG; control) serum or with varying concentrations ...
<p>Insulin released into culture medium from day 0 to 3 and from day 12 to 15 and also in extracts c...
<p>(A, C-F) INS-1E cells and (B) isolated mouse islets were cultured in the presence of test substan...
<p>(A–D) INS-1 cells were cultured for 14 days. (E and F) under normal-culture-glucose (11.2 mmol/l;...
The presence and biological significance of circulating glycated insulin has been evaluated by high-...
The purpose of the present study was to evaluate the direct effects of advanced glycation end produc...
<p>(<b>A</b>) The indicated cells were preincubated with the PI-3 kinase inhibitor LY294002 for 1 ho...
<p>(A) INS-1 cells were pretreated with RAGE antibody for 1 h and then treated with nonglycated (NG)...