From: Baicalein Inhibits Amadori-Glycated Albumin-Induced MCP-1 Expression in Retinal Ganglion Cells via a MicroRNA-124–Dependent Mechanism Invest. Ophthalmol.

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Date of download: 6/22/2016 The Association for Research in Vision and Ophthalmology Copyright © All rights reserved. From: Simultaneous Cell Death.
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From: Baicalein Inhibits Amadori-Glycated Albumin-Induced MCP-1 Expression in Retinal Ganglion Cells via a MicroRNA-124–Dependent Mechanism Invest. Ophthalmol. Vis. Sci.. 2015;56(10):5844-5853. doi:10.1167/iovs.15-17444 Figure Legend: Baicalein attenuated expression of MCP-1 induced by AGA in cultured rat RGCs. (A, B) Amadori-glycated albumin stimulation increased expression of MCP-1 in cultured rat RGCs. Retinal ganglion cells were incubated with the indicated concentrations of AGA for 24 hours (A) or 750 μg/mL AGA for the indicated times (B). Amadori-glycated albumin treatment increased expression of MCP-1 in a dose- and time-dependent manner. (C, D) Retinal ganglion cells were preincubated with the indicated concentrations of baicalein for 1 hour before incubation with 750 μg/mL AGA for 24 hours or 750 μg/mL AGA for 24 hours, and we also added 10 μg/mL baicalein for the indicated times. Baicalein decreased the AGA-induced expression of MCP-1 protein in a dose- and time-dependent manner. Expression levels of MCP-1 protein were determined by ELISA. (E) Direct knockdown of Dicer downregulated the expression of Dicer, determined by Western blot analysis (left). Retinal ganglion cells were transfected with control siRNA or Dicer siRNA for 24 hours and stimulated with 750 μg/mL AGA in the presence or absence of 10 μg/mL baicalein. Monocyte chemotactic protein-1 expression levels were measured by ELISA and qRT-PCR. Percentages were calculated using AGA alone as 100%. The baicalein on AGA-induced MCP-1 protein-to-mRNA inhibition ratio was reduced from 76.3% to 31.7% and from 87.5% to 56.1% by knockdown of Dicer, respectively. Results were statistically significant (*P < 0.01). Error bars denote SEM. Date of download: 10/21/2017 The Association for Research in Vision and Ophthalmology Copyright © 2017. All rights reserved.