The role of the thioredoxin/thioredoxin reductase system in the metabolic syndrome: towards a possible prognostic marker?

Mammalian thioredoxin reductase (TrxR) is a selenoprotein with three existing isoenzymes (TrxR1, TrxR2, and TrxR3), which is found primarily intracellularly but also in extracellular fluids. The main substrate thioredoxin (Trx) is similarly found (as Trx1 and Trx2) in various intracellular compartments, in blood plasma, and is the cell’s major disulfide reductase. Thioredoxin reductase is necessary as a NADPH-dependent reducing agent in biochemical reactions involving Trx. Genetic and environmental factors like selenium status influence the activity of TrxR. Research shows that the Trx/TrxR system plays a significant role in the physiology of the adipose tissue, in carbohydrate metabolism, insulin production and sensitivity, blood pressure regulation, inflammation, chemotactic activity of macrophages, and atherogenesis. Based on recent research, it has been reported that the modulation of the Trx/TrxR system may be considered as a new target in the management of the metabolic syndrome, insulin resistance, and type 2 diabetes, as well as in the treatment of hypertension and atherosclerosis. In this review evidence about a possible role of this system as a marker of the metabolic syndrome is reported. © 2018, Springer International Publishing AG, part of Springer Nature.

Авторы
Tinkov A.A. 1, 2, 3 , Bjørklund G.4 , Skalny A.V. 1, 2, 5, 6 , Holmgren A.7 , Skalnaya M.G. 2 , Chirumbolo S.8 , Aaseth J.9, 10
Издательство
Birkhauser Verlag AG
Номер выпуска
9
Язык
Английский
Страницы
1567-1586
Статус
Опубликовано
Том
75
Год
2018
Организации
  • 1 Yaroslavl State University, Yaroslavl, Russian Federation
  • 2 Peoples’ Friendship University of Russia (RUDN University), Moscow, Russian Federation
  • 3 Institute of Cellular and Intracellular Symbiosis, Russian Academy of Sciences, Orenburg, Russian Federation
  • 4 Council for Nutritional and Environmental Medicine, Toften 24, Mo i Rana, 8610, Norway
  • 5 Trace Element Institute for UNESCO, Lyon, France
  • 6 Orenburg State University, Orenburg, Russian Federation
  • 7 Department of Medical Biochemistry and Biophysics (MBB), Karolinska Institute, Stockholm, Sweden
  • 8 Department of Neurological and Movement Sciences, University of Verona, Verona, Italy
  • 9 Research Department, Innlandet Hospital Trust, Brumunddal, Norway
  • 10 Inland Norway University of Applied Sciences, Elverum, Norway
Ключевые слова
Diabetes; Obesity; Selenium; Thioredoxin interacting protein; Thioredoxin reductase
Дата создания
19.10.2018
Дата изменения
19.10.2018
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/6703/
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Yeh W.W., Fraser I.P., Jumes P., Petry A., Lepeleire I.D., Robberechts M., Reitmann C., Huang X., Guo Z., Panebianco D., Nachbar R.B., O'Mara E., Wagner J.A., Butterton J.R., Dutko F.J., Moiseev V., Kobalava Z., Hüser A., Visan S., Schwabe C., Gane E., Popa S., Ghicavii N., Uhle M., Wagner F., Van Dyck K.
Clinical Therapeutics. Том 40. 2018. С. 704-718.e6