author_facet Schmelzer, Constance
Lorenz, Gerti
Lindner, Inka
Rimbach, Gerald
Niklowitz, Petra
Menke, Thomas
Döring, Frank
Schmelzer, Constance
Lorenz, Gerti
Lindner, Inka
Rimbach, Gerald
Niklowitz, Petra
Menke, Thomas
Döring, Frank
author Schmelzer, Constance
Lorenz, Gerti
Lindner, Inka
Rimbach, Gerald
Niklowitz, Petra
Menke, Thomas
Döring, Frank
spellingShingle Schmelzer, Constance
Lorenz, Gerti
Lindner, Inka
Rimbach, Gerald
Niklowitz, Petra
Menke, Thomas
Döring, Frank
BioFactors
Effects of Coenzyme Q10 on TNF‐α secretion in human and murine monocytic cell lines
Clinical Biochemistry
Molecular Medicine
General Medicine
Biochemistry
author_sort schmelzer, constance
spelling Schmelzer, Constance Lorenz, Gerti Lindner, Inka Rimbach, Gerald Niklowitz, Petra Menke, Thomas Döring, Frank 0951-6433 1872-8081 Wiley Clinical Biochemistry Molecular Medicine General Medicine Biochemistry http://dx.doi.org/10.1002/biof.5520310104 <jats:title>Abstract</jats:title><jats:p>Studies in humans and cell culture as well as bioinformatics suggested that Coenzyme Q<jats:sub>10</jats:sub> (CoQ<jats:sub>10</jats:sub> ) functions as an anti‐inflammatory molecule. Here we studied the influence of CoQ<jats:sub>10</jats:sub> (Kaneka QTM ) on secretion of the pro‐inflammatory 10 cytokine tumor necrosis factor‐alpha (TNF‐α) by using the human and murine monocytic cell lines TH P‐1 and RAW264.7 expressing human apolipoprotein E3 (apoE3) or pro‐inflammatory apoE4. Incubation of cells with physiological (0.1–10 μM) and supra‐physiological (&gt; 10 to ≤ 100 μM) concentrations of CoQ<jats:sub>10</jats:sub> led to an intracellular accumulation of its reduced form without any cytotoxic effects. Stimulation of cell models with lipopolysaccharide (LPS) resulted in a substantially release of TNF‐α. When THP‐1 cells were pre‐incubated with 10 μM CoQ<jats:sub>10</jats:sub>, the LPS‐induced TNF‐α release was significantly decreased to 72 ± 32%. This effect is similar to those obtained by 10 μM N‐Acetyl‐Cysteine, a well known reference antioxidant. In RAW264.7‐apoE3 and ‐apoE4 cells, significant reductions of LPS‐induced TNF‐α secretion to 73.3 ± 2.8% and 74.7 ± 8.9% were found with 2.5 μM and 75 μM CoQ<jats:sub>10</jats:sub>, respectively. In conclusion, CoQ<jats:sub>10</jats:sub> has moderate anti‐inflammatory effects in two monocytic cell lines which could be mediated by its antioxidant activity.</jats:p> Effects of Coenzyme Q<sub>10</sub> on TNF‐α secretion in human and murine monocytic cell lines BioFactors
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title Effects of Coenzyme Q10 on TNF‐α secretion in human and murine monocytic cell lines
title_unstemmed Effects of Coenzyme Q10 on TNF‐α secretion in human and murine monocytic cell lines
title_full Effects of Coenzyme Q10 on TNF‐α secretion in human and murine monocytic cell lines
title_fullStr Effects of Coenzyme Q10 on TNF‐α secretion in human and murine monocytic cell lines
title_full_unstemmed Effects of Coenzyme Q10 on TNF‐α secretion in human and murine monocytic cell lines
title_short Effects of Coenzyme Q10 on TNF‐α secretion in human and murine monocytic cell lines
title_sort effects of coenzyme q<sub>10</sub> on tnf‐α secretion in human and murine monocytic cell lines
topic Clinical Biochemistry
Molecular Medicine
General Medicine
Biochemistry
url http://dx.doi.org/10.1002/biof.5520310104
publishDate 2007
physical 35-41
description <jats:title>Abstract</jats:title><jats:p>Studies in humans and cell culture as well as bioinformatics suggested that Coenzyme Q<jats:sub>10</jats:sub> (CoQ<jats:sub>10</jats:sub> ) functions as an anti‐inflammatory molecule. Here we studied the influence of CoQ<jats:sub>10</jats:sub> (Kaneka QTM ) on secretion of the pro‐inflammatory 10 cytokine tumor necrosis factor‐alpha (TNF‐α) by using the human and murine monocytic cell lines TH P‐1 and RAW264.7 expressing human apolipoprotein E3 (apoE3) or pro‐inflammatory apoE4. Incubation of cells with physiological (0.1–10 μM) and supra‐physiological (&gt; 10 to ≤ 100 μM) concentrations of CoQ<jats:sub>10</jats:sub> led to an intracellular accumulation of its reduced form without any cytotoxic effects. Stimulation of cell models with lipopolysaccharide (LPS) resulted in a substantially release of TNF‐α. When THP‐1 cells were pre‐incubated with 10 μM CoQ<jats:sub>10</jats:sub>, the LPS‐induced TNF‐α release was significantly decreased to 72 ± 32%. This effect is similar to those obtained by 10 μM N‐Acetyl‐Cysteine, a well known reference antioxidant. In RAW264.7‐apoE3 and ‐apoE4 cells, significant reductions of LPS‐induced TNF‐α secretion to 73.3 ± 2.8% and 74.7 ± 8.9% were found with 2.5 μM and 75 μM CoQ<jats:sub>10</jats:sub>, respectively. In conclusion, CoQ<jats:sub>10</jats:sub> has moderate anti‐inflammatory effects in two monocytic cell lines which could be mediated by its antioxidant activity.</jats:p>
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author Schmelzer, Constance, Lorenz, Gerti, Lindner, Inka, Rimbach, Gerald, Niklowitz, Petra, Menke, Thomas, Döring, Frank
author_facet Schmelzer, Constance, Lorenz, Gerti, Lindner, Inka, Rimbach, Gerald, Niklowitz, Petra, Menke, Thomas, Döring, Frank, Schmelzer, Constance, Lorenz, Gerti, Lindner, Inka, Rimbach, Gerald, Niklowitz, Petra, Menke, Thomas, Döring, Frank
author_sort schmelzer, constance
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description <jats:title>Abstract</jats:title><jats:p>Studies in humans and cell culture as well as bioinformatics suggested that Coenzyme Q<jats:sub>10</jats:sub> (CoQ<jats:sub>10</jats:sub> ) functions as an anti‐inflammatory molecule. Here we studied the influence of CoQ<jats:sub>10</jats:sub> (Kaneka QTM ) on secretion of the pro‐inflammatory 10 cytokine tumor necrosis factor‐alpha (TNF‐α) by using the human and murine monocytic cell lines TH P‐1 and RAW264.7 expressing human apolipoprotein E3 (apoE3) or pro‐inflammatory apoE4. Incubation of cells with physiological (0.1–10 μM) and supra‐physiological (&gt; 10 to ≤ 100 μM) concentrations of CoQ<jats:sub>10</jats:sub> led to an intracellular accumulation of its reduced form without any cytotoxic effects. Stimulation of cell models with lipopolysaccharide (LPS) resulted in a substantially release of TNF‐α. When THP‐1 cells were pre‐incubated with 10 μM CoQ<jats:sub>10</jats:sub>, the LPS‐induced TNF‐α release was significantly decreased to 72 ± 32%. This effect is similar to those obtained by 10 μM N‐Acetyl‐Cysteine, a well known reference antioxidant. In RAW264.7‐apoE3 and ‐apoE4 cells, significant reductions of LPS‐induced TNF‐α secretion to 73.3 ± 2.8% and 74.7 ± 8.9% were found with 2.5 μM and 75 μM CoQ<jats:sub>10</jats:sub>, respectively. In conclusion, CoQ<jats:sub>10</jats:sub> has moderate anti‐inflammatory effects in two monocytic cell lines which could be mediated by its antioxidant activity.</jats:p>
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spelling Schmelzer, Constance Lorenz, Gerti Lindner, Inka Rimbach, Gerald Niklowitz, Petra Menke, Thomas Döring, Frank 0951-6433 1872-8081 Wiley Clinical Biochemistry Molecular Medicine General Medicine Biochemistry http://dx.doi.org/10.1002/biof.5520310104 <jats:title>Abstract</jats:title><jats:p>Studies in humans and cell culture as well as bioinformatics suggested that Coenzyme Q<jats:sub>10</jats:sub> (CoQ<jats:sub>10</jats:sub> ) functions as an anti‐inflammatory molecule. Here we studied the influence of CoQ<jats:sub>10</jats:sub> (Kaneka QTM ) on secretion of the pro‐inflammatory 10 cytokine tumor necrosis factor‐alpha (TNF‐α) by using the human and murine monocytic cell lines TH P‐1 and RAW264.7 expressing human apolipoprotein E3 (apoE3) or pro‐inflammatory apoE4. Incubation of cells with physiological (0.1–10 μM) and supra‐physiological (&gt; 10 to ≤ 100 μM) concentrations of CoQ<jats:sub>10</jats:sub> led to an intracellular accumulation of its reduced form without any cytotoxic effects. Stimulation of cell models with lipopolysaccharide (LPS) resulted in a substantially release of TNF‐α. When THP‐1 cells were pre‐incubated with 10 μM CoQ<jats:sub>10</jats:sub>, the LPS‐induced TNF‐α release was significantly decreased to 72 ± 32%. This effect is similar to those obtained by 10 μM N‐Acetyl‐Cysteine, a well known reference antioxidant. In RAW264.7‐apoE3 and ‐apoE4 cells, significant reductions of LPS‐induced TNF‐α secretion to 73.3 ± 2.8% and 74.7 ± 8.9% were found with 2.5 μM and 75 μM CoQ<jats:sub>10</jats:sub>, respectively. In conclusion, CoQ<jats:sub>10</jats:sub> has moderate anti‐inflammatory effects in two monocytic cell lines which could be mediated by its antioxidant activity.</jats:p> Effects of Coenzyme Q<sub>10</sub> on TNF‐α secretion in human and murine monocytic cell lines BioFactors
spellingShingle Schmelzer, Constance, Lorenz, Gerti, Lindner, Inka, Rimbach, Gerald, Niklowitz, Petra, Menke, Thomas, Döring, Frank, BioFactors, Effects of Coenzyme Q10 on TNF‐α secretion in human and murine monocytic cell lines, Clinical Biochemistry, Molecular Medicine, General Medicine, Biochemistry
title Effects of Coenzyme Q10 on TNF‐α secretion in human and murine monocytic cell lines
title_full Effects of Coenzyme Q10 on TNF‐α secretion in human and murine monocytic cell lines
title_fullStr Effects of Coenzyme Q10 on TNF‐α secretion in human and murine monocytic cell lines
title_full_unstemmed Effects of Coenzyme Q10 on TNF‐α secretion in human and murine monocytic cell lines
title_short Effects of Coenzyme Q10 on TNF‐α secretion in human and murine monocytic cell lines
title_sort effects of coenzyme q<sub>10</sub> on tnf‐α secretion in human and murine monocytic cell lines
title_unstemmed Effects of Coenzyme Q10 on TNF‐α secretion in human and murine monocytic cell lines
topic Clinical Biochemistry, Molecular Medicine, General Medicine, Biochemistry
url http://dx.doi.org/10.1002/biof.5520310104