Yuri Shatalin

Dr. Yuri Shatalin

Institute of Theoretical and Experimental Biophysics, Russian Academy of Sciences
orcid

Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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8 August 2021 in Antioxidants
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Journal Article
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VSVictoria Shubina
Victoria Shubina
KVKozina Victoria
Kozina Victoria
Yuri ShatalinYuri Shatalin
Yuri Shatalin
It is known that flavonoids can react with toxic carbonyl compounds in the process of the storage, aging, and digestion of flavonoid-rich foods and beverages. However, the effect of these reactions on the antioxidant properties of the polyphenolic fraction and the properties of the resulting products remain poorly studied. The aim of the present work was to study the antioxidant activity of quercetin, taxifolin, catechin, eriodictyol, hesperetin, naringenin and a product of the condensation of taxifolin with glyoxylic acid, as well as to reveal the structure–activity relationship of these polyphenols. It was found that flavonoids containing the catechol moiety exhibited higher antioxidant activity than hesperetin and naringenin. The product showed the highest hydrogen peroxide scavenging activity, a lower metal-reducing and a higher iron-binding ability than catechol-containing flavonoids, and a lipid peroxidation inhibitory activity comparable with that of taxifolin. Thus, the condensation of flavonoids with toxic carbonyl compounds might lead to the formation of products exhibiting high antioxidant activity. Meanwhile, the conditions under which parent flavonoids and their products exhibit the maximal antioxidant activity may differ. The data suggest that the antioxidant profile of the polyphenolic fraction and bioavailability of polyphenols, carbonyl compounds, and metal ions may change when these reactions occur.

31 May 2022 in Biochimica et Biophysica Acta (BBA) - General Subjects
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Journal Article
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MSMarina E. Solovieva
Marina E. Solovieva
Yuri ShatalinYuri Shatalin
Yuri Shatalin
IOIrina Odinokova
Irina Odinokova
OKOlga Krestinina
Olga Krestinina
YBYulia Baburina
Yulia Baburina
VAVladimir Akatov
Vladimir Akatov

1 January 2020 in Biomolecules
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MSMarina E. Solovieva
Marina E. Solovieva
Yuri ShatalinYuri Shatalin
Yuri Shatalin
Roman S. FadeevRoman S. Fadeev
Roman S. Fadeev
OKOlga V Krestinina
Olga V Krestinina
YBYulia Baburina
Yulia Baburina
VAVladimir S. Akatov
Vladimir S. Akatov
We have shown that hydroxycobalamin (vitamin B12b) increases the toxicity of diethyldithiocarbamate (DDC) to tumor cells by catalyzing the formation of disulfiram (DSF) oxi-derivatives. The purpose of this study was to elucidate the mechanism of tumor cell death induced by the combination DDC + B12b. It was found that cell death induced by DDC + B12b differed from apoptosis, autophagy, and necrosis. During the initiation of cell death, numerous vacuoles formed from ER cisterns in the cytoplasm, and cell death was partially suppressed by the inhibitors of protein synthesis and folding, the IP3 receptor inhibitor as well as by thiols. At this time, a short-term rise in the expression of ER-stress markers BiP and PERK with a steady increase in the expression of CHOP were detected. After the vacuolization of the cytoplasm, functional disorders of mitochondria and an increase in the generation of superoxide anion in them occurred. Taken together, the results obtained indicate that DDC and B12b used in combination exert a synergistic toxic effect on tumor cells by causing severe ER stress, extensive ER vacuolization, and inhibition of apoptosis, which ultimately leads to the induction of paraptosis-like cell death.

22 November 2012 in Bulletin of Experimental Biology and Medicine
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VSV. S. Shubina
V. S. Shubina
Yuri ShatalinYuri Shatalin
Yuri Shatalin

10 May 2022 in Dyes and Pigments
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Journal Article
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ASAnton L. Shatsauskas
Anton L. Shatsauskas
Yuri ShatalinYuri Shatalin
Yuri Shatalin
VSVictoria S. Shubina
Victoria S. Shubina
SCSergei A. Chernenko
Sergei A. Chernenko
AKAnastasia S. Kostyuchenko
Anastasia S. Kostyuchenko
AFAlexander S. Fisyuk
Alexander S. Fisyuk

Verified
Journal Article
Open access
PDF file
VSVictoria S. Shubina
Victoria S. Shubina
KVKozina Victoria
Kozina Victoria
Yuri ShatalinYuri Shatalin
Yuri Shatalin
During the storage, processing, and digestion of flavonoid-rich foods and beverages, a condensation of flavonoids with toxic carbonyl compounds occurs. The effect of the resulting products on cells remains largely unknown. The aim of the present study was to evaluate the effects of quercetin, taxifolin, catechin, eriodictyol, hesperetin, naringenin, and a condensation product of taxifolin with glyoxylic acid on the oxidative burst of neutrophils. It was found that the flavonoids and the condensation product inhibited the total production of ROS. Flavonoids decreased both the intra and extracellular ROS production. The condensation product had no effect on intracellular ROS production but effectively inhibited the extracellular production of ROS. Thus, the condensation of flavonoids with toxic carbonyl compounds may lead to the formation of compounds exhibiting potent inhibitory effects on the oxidative burst of neutrophils. The data also suggest that, during these reactions, the influence of a fraction of flavonoids and their polyphenolic derivatives on cellular functions may change. On the whole, the results of the study provide a better understanding of the effects of polyphenols on human health. In addition, these results reveal the structure–activity relationship of these polyphenols and may be useful in a search for new therapeutic agents against diseases associated with oxidative stress.