2012
DOI: 10.18097/pbmc20125801077
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A new approach to studying the autoxidation of adrenaline: possibility of the determination of superoxide dismutase activity and the antioxidant properties of various preparations by polarography

Abstract: The reaction of adrenaline autoxidation in an alkaline buffer with the formation of superoxide radicals and the product of its oxidation, adrenochrome, which models the quinoid pathway of adrenaline conversion in the body, is accompanied by oxygen consumption. This reaction is applicable for polarographic determination of the activity of superoxide dismutase and the antioxidant properties of biological and chemical compounds, it is based on evaluation of the latent period and the rate of oxygen consumption, wh… Show more

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Cited by 26 publications
(11 citation statements)
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References 22 publications
(36 reference statements)
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“…The intensity of lipid peroxidation (LPO) was estimated by the MDA level in plasma and erythrocytes in accordance with the methods by Uchiyama and Mihara [ 28 ]. Superoxide dismutase activity (EC 1.15.1.1) was measured in erythrocytes using inhibition of adrenaline auto-oxidation [ 29 ]. Catalase activity (EC 1.11.1.6) was determined by spectrophotometry based on the decomposition of hydrogen peroxide by the catalase [ 30 ].…”
Section: Methodsmentioning
confidence: 99%
“…The intensity of lipid peroxidation (LPO) was estimated by the MDA level in plasma and erythrocytes in accordance with the methods by Uchiyama and Mihara [ 28 ]. Superoxide dismutase activity (EC 1.15.1.1) was measured in erythrocytes using inhibition of adrenaline auto-oxidation [ 29 ]. Catalase activity (EC 1.11.1.6) was determined by spectrophotometry based on the decomposition of hydrogen peroxide by the catalase [ 30 ].…”
Section: Methodsmentioning
confidence: 99%
“…Erythrocytes were washed twice with 0.9% NaCl by centrifugation for 10 min at 1600 g. The intensity of lipid peroxidation (LPO) was estimated by the MDA level in plasma and erythrocytes following the methods by Uchiyama and Mihara [ 55 ]. Superoxide dismutase activity (EC 1.15.1.1) was measured in erythrocytes using inhibition of adrenaline auto-oxidation [ 56 ]. Catalase activity (EC 1.11.1.6) was determined by spectrophotometry based on the decomposition of hydrogen peroxide by the catalase [ 57 ].…”
Section: Methodsmentioning
confidence: 99%
“…The intensity of lipid peroxidation (LPO) was estimated by the MDA level in plasma and erythrocytes following the methods by Uchiyama and Mihara [ 44 ]. Superoxide dismutase activity (EC 1.15.1.1) was measured in erythrocytes using inhibition of adrenaline auto-oxidation [ 45 ]. Catalase activity (EC 1.11.1.6) was determined by spectrophotometry based on the decomposition of hydrogen peroxide by the catalase [ 46 ].…”
Section: Methodsmentioning
confidence: 99%