2019
DOI: 10.3897/rrpharmacology.5.34710
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Pharmacological modulation of cell functional activity with valproic acid and erythropoietin

Abstract: Introduction: Valproic acid (VA) is carboxylic acid with a branched chain, which is used as an antiepileptic drug. Valproic acid influence on cells in vivo: VA, which is an antiepileptic drug, is also a teratogen, which causes defects of a neural tube and an axial skeleton, although the mechanisms are not yet fully clear. Valproic acid influence on mesenchymal stem cells (MSC) in vitro: It is shown that valproic acid reduces the intracellular level of oxygen active forms. Valproic… Show more

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Cited by 2 publications
(4 citation statements)
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“…c at a temperature of 20 ° C. For the hydrolytic digestion of the protein, trypsin was used in an enzyme / total protein weight ratio of 1/50 and incubated overnight at 37 °C. The resulting mixture of peptides was dried in a centrifugal concentrator at 45 ° C for 30 min, the peptides were redissolved in 20 μ L of 0.1% formic acid and subjected to further mass spectrometric analysis 7,8 . Proteomic analysis of peptides was carried out using an Ultimate 3000 RSLCnano chromatographic HPLC system (Thermo Scientific, USA) connected to a Q-exactive HFX mass spectrometer (Thermo Scientific, USA) [13][14][15][16][17] .…”
Section: Sp23l39mentioning
confidence: 99%
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“…c at a temperature of 20 ° C. For the hydrolytic digestion of the protein, trypsin was used in an enzyme / total protein weight ratio of 1/50 and incubated overnight at 37 °C. The resulting mixture of peptides was dried in a centrifugal concentrator at 45 ° C for 30 min, the peptides were redissolved in 20 μ L of 0.1% formic acid and subjected to further mass spectrometric analysis 7,8 . Proteomic analysis of peptides was carried out using an Ultimate 3000 RSLCnano chromatographic HPLC system (Thermo Scientific, USA) connected to a Q-exactive HFX mass spectrometer (Thermo Scientific, USA) [13][14][15][16][17] .…”
Section: Sp23l39mentioning
confidence: 99%
“…During the annotation, a functional analysis algorithm was used to identify statistically significant representation of certain groups of proteins among all genes / proteins in the sample under study. The statistical significance was assessed using the probability p-value, as well as the Adjusted P-value, which was calculated taking into account the multiplicity of comparison [7][8][9][10][11][12][13] . The groups for which the Adjusted P-value was less than 0.001 were considered significant protein groups in the classifications.…”
Section: Sp23l39mentioning
confidence: 99%
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