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The role of sodium pyruvate in mitigating the cytotoxic effects of vanadium on CHO-K1 cells
by
Wnuk, Ewa
, Zwolak, Iwona
, Kochanowicz, Elżbieta
in
631/154/570
/ 631/45/321
/ Adenosine Triphosphate - metabolism
/ Animals
/ Annexin V
/ Antioxidant
/ Antioxidants
/ Antioxidants - pharmacology
/ Apoptosis
/ Apoptosis - drug effects
/ Bioluminescence
/ Caspase-3
/ Cell proliferation
/ Cell Proliferation - drug effects
/ Cell Survival - drug effects
/ Cells
/ CHO Cells
/ Cricetinae
/ Cricetulus
/ Cytotoxicity
/ Glutathione
/ Glutathione - metabolism
/ Humanities and Social Sciences
/ Metal
/ Mice
/ multidisciplinary
/ Necrosis
/ Occupational exposure
/ Oxidants
/ Oxidative stress
/ Oxidative Stress - drug effects
/ Oxidizing agents
/ Pyruvate
/ Pyruvic acid
/ Pyruvic Acid - pharmacology
/ Reagents
/ Risk factors
/ Science
/ Science (multidisciplinary)
/ Sodium
/ Sodium pyruvate
/ Steel production
/ Toxicity
/ Vanadium
/ Vanadium - toxicity
/ Vanadium Compounds
/ Vanadyl sulfate
2025
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The role of sodium pyruvate in mitigating the cytotoxic effects of vanadium on CHO-K1 cells
by
Wnuk, Ewa
, Zwolak, Iwona
, Kochanowicz, Elżbieta
in
631/154/570
/ 631/45/321
/ Adenosine Triphosphate - metabolism
/ Animals
/ Annexin V
/ Antioxidant
/ Antioxidants
/ Antioxidants - pharmacology
/ Apoptosis
/ Apoptosis - drug effects
/ Bioluminescence
/ Caspase-3
/ Cell proliferation
/ Cell Proliferation - drug effects
/ Cell Survival - drug effects
/ Cells
/ CHO Cells
/ Cricetinae
/ Cricetulus
/ Cytotoxicity
/ Glutathione
/ Glutathione - metabolism
/ Humanities and Social Sciences
/ Metal
/ Mice
/ multidisciplinary
/ Necrosis
/ Occupational exposure
/ Oxidants
/ Oxidative stress
/ Oxidative Stress - drug effects
/ Oxidizing agents
/ Pyruvate
/ Pyruvic acid
/ Pyruvic Acid - pharmacology
/ Reagents
/ Risk factors
/ Science
/ Science (multidisciplinary)
/ Sodium
/ Sodium pyruvate
/ Steel production
/ Toxicity
/ Vanadium
/ Vanadium - toxicity
/ Vanadium Compounds
/ Vanadyl sulfate
2025
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The role of sodium pyruvate in mitigating the cytotoxic effects of vanadium on CHO-K1 cells
by
Wnuk, Ewa
, Zwolak, Iwona
, Kochanowicz, Elżbieta
in
631/154/570
/ 631/45/321
/ Adenosine Triphosphate - metabolism
/ Animals
/ Annexin V
/ Antioxidant
/ Antioxidants
/ Antioxidants - pharmacology
/ Apoptosis
/ Apoptosis - drug effects
/ Bioluminescence
/ Caspase-3
/ Cell proliferation
/ Cell Proliferation - drug effects
/ Cell Survival - drug effects
/ Cells
/ CHO Cells
/ Cricetinae
/ Cricetulus
/ Cytotoxicity
/ Glutathione
/ Glutathione - metabolism
/ Humanities and Social Sciences
/ Metal
/ Mice
/ multidisciplinary
/ Necrosis
/ Occupational exposure
/ Oxidants
/ Oxidative stress
/ Oxidative Stress - drug effects
/ Oxidizing agents
/ Pyruvate
/ Pyruvic acid
/ Pyruvic Acid - pharmacology
/ Reagents
/ Risk factors
/ Science
/ Science (multidisciplinary)
/ Sodium
/ Sodium pyruvate
/ Steel production
/ Toxicity
/ Vanadium
/ Vanadium - toxicity
/ Vanadium Compounds
/ Vanadyl sulfate
2025
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The role of sodium pyruvate in mitigating the cytotoxic effects of vanadium on CHO-K1 cells
Journal Article
The role of sodium pyruvate in mitigating the cytotoxic effects of vanadium on CHO-K1 cells
2025
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Overview
Vanadium is a hazardous, pro-oxidant element that contributes to environmental pollution and has been reported as a risk factor for human health through occupational or environmental exposure. Pyruvate, on the other hand, is a natural alpha-keto acid with exceptional antioxidant and cytoprotective properties. Therefore, the aim of this study was to evaluate the mitigating effect of exogenous pyruvate against vanadium-induced toxicity in cultured Chinese hamster ovary (CHO)-K1 cells. To this end, CHO-K1 cells were exposed to 100 μM vanadyl sulfate (VOSO
4
) for 24 h in the presence of 4.5 and 8 mM sodium pyruvate. Cell proliferation and morphological changes, cellular ATP levels, antioxidant stress (GSH) levels and apoptosis markers (caspase 3, 9, annexin V binding) were assessed to investigate the effect of sodium pyruvate on VOSO
4
-induced damage in CHO-K1 cells. The results showed that VOSO
4
induced morphological changes, inhibited cell proliferation, decreased cellular ATP and reduced glutathione levels. Co-treatment of VOSO
4
-intoxicated CHO-K1 cells with sodium pyruvate significantly reduced these cytotoxic effects. Analysis of apoptosis and necrosis showed that VOSO
4
slightly induced apoptosis and necrosis, and exogenous pyruvate inhibited the cytotoxicity of the tested vanadium dose in CHO-K1 cells, mainly by reducing the necrosis effect. The cytoprotective effect of exogenous pyruvate was also confirmed in normal mouse fibroblast (NIH/3T3) cells demonstrating that the protective properties of pyruvate are not cell specific.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
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