<p>(A) BV2 cells were treated with different doses of rotenone or LPS for 24 hours. The TNFα levels in the cultured media were measured using ELISA assays. The data are presented as the mean ± S.E.M. n = 3, **p<0.01, one-way ANOVA. (B) Immunoblot analysis to detect iNOS expression in the BV2 cells treated with rotenone or LPS. (C) Quantitative analysis of the data from (B), showing the density of iNOS relative to that of the loading control (tubulin). The data are presented as the mean ± S.E.M. n = 3, **p<0.01, ***p<0.001, one-way ANOVA.</p
<p>(<b>A</b>) BV-2 cells were cultured in a 24-well plate at 5×10<sup>4</sup> cells/well and were ex...
<p>Different proliferation rates of exponentially growing cell populations exposed to increasing amo...
<p>(A, B, C) Cells were exposed to 50 nM Rotenone over 120 hours in culture and DNA content was dete...
<p>(A) Various doses of rotenone or LPS were administered to BV2 cells as indicated for 6 hours or 1...
<p>(A) BV2 cells were treated with different doses of rotenone for 6 hours or 1 µg/mL LPS for 1 hour...
<p>(A) BV2 cells treated with 1 µM rotenone for 24 hours or 1 µg/mL LPS for 24 hours or co-treated w...
<p><b>A.</b> Primary microglia were stimulated with rotenone (upper) or MPO (lower) in the presence ...
<p>HEK 293T cells were treated with 1 μM rotenone alone or in combination with 0.1 μg/ml or 1 μg/ml ...
<p><b>a) Less Bax translocated to mitochondria in 14-3-3θ cells in response to rotenone.</b> After t...
<p>(<b>A, C, E</b>) Expression of iNOS, TNF and IL6 at mRNA level in BV-2 cells. Expression of iNOS,...
<p>A. cells were treated with 0~100 μmol/L (μM) rotenone for 24 hours. Cell viability was measured a...
<p>A. BV2 microglia were treated with 30 nM rotenone (Rot, <i>a</i>) or 100 ng/ml MPO (<i>b</i>) in ...
<p><b>A.</b> Primary mixed glial cells from <i>Mpo<sup>−/−</sup></i> mice were mock-treated or treat...
<p>(<b>A</b>) pro-inflammatory cytokine TNF-α level and (<b>B</b>) NO level were examined in midbrai...
Neuroinflammation, whose distinctive sign is the activation of microglia, is supposed to play a key...
<p>(<b>A</b>) BV-2 cells were cultured in a 24-well plate at 5×10<sup>4</sup> cells/well and were ex...
<p>Different proliferation rates of exponentially growing cell populations exposed to increasing amo...
<p>(A, B, C) Cells were exposed to 50 nM Rotenone over 120 hours in culture and DNA content was dete...
<p>(A) Various doses of rotenone or LPS were administered to BV2 cells as indicated for 6 hours or 1...
<p>(A) BV2 cells were treated with different doses of rotenone for 6 hours or 1 µg/mL LPS for 1 hour...
<p>(A) BV2 cells treated with 1 µM rotenone for 24 hours or 1 µg/mL LPS for 24 hours or co-treated w...
<p><b>A.</b> Primary microglia were stimulated with rotenone (upper) or MPO (lower) in the presence ...
<p>HEK 293T cells were treated with 1 μM rotenone alone or in combination with 0.1 μg/ml or 1 μg/ml ...
<p><b>a) Less Bax translocated to mitochondria in 14-3-3θ cells in response to rotenone.</b> After t...
<p>(<b>A, C, E</b>) Expression of iNOS, TNF and IL6 at mRNA level in BV-2 cells. Expression of iNOS,...
<p>A. cells were treated with 0~100 μmol/L (μM) rotenone for 24 hours. Cell viability was measured a...
<p>A. BV2 microglia were treated with 30 nM rotenone (Rot, <i>a</i>) or 100 ng/ml MPO (<i>b</i>) in ...
<p><b>A.</b> Primary mixed glial cells from <i>Mpo<sup>−/−</sup></i> mice were mock-treated or treat...
<p>(<b>A</b>) pro-inflammatory cytokine TNF-α level and (<b>B</b>) NO level were examined in midbrai...
Neuroinflammation, whose distinctive sign is the activation of microglia, is supposed to play a key...
<p>(<b>A</b>) BV-2 cells were cultured in a 24-well plate at 5×10<sup>4</sup> cells/well and were ex...
<p>Different proliferation rates of exponentially growing cell populations exposed to increasing amo...
<p>(A, B, C) Cells were exposed to 50 nM Rotenone over 120 hours in culture and DNA content was dete...