4.4 Review

Glucose transporters in cardiovascular system in health and disease

期刊

PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY
卷 472, 期 9, 页码 1385-1399

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s00424-020-02444-8

关键词

Cardiac metabolism; GLUT; SGLT; SMIT1; Akt; AMPK; Glucotoxicity; Diabetic cardiomyopathy; Cardiac hypertrophy; Heart failure

资金

  1. Fonds National de la Recherche Scientifique etMedicale (FNRS), Belgium
  2. Action de Recherche Concertee de la Communaute Wallonie-Bruxelles, Belgium [ARC 16/21-074]
  3. Astra Zeneca
  4. Fund for Scientific Research in Industry and Agriculture, Belgium

向作者/读者索取更多资源

Glucose transporters are essential for the heart to sustain its function. Due to its nature as a high energy-consuming organ, the heart needs to catabolize a huge quantity of metabolic substrates. For optimized energy production, the healthy heart constantly switches between various metabolites in accordance with substrate availability and hormonal status. This metabolic flexibility is essential for the maintenance of cardiac function. Glucose is part of the main substrates catabolized by the heart and its use is fine-tuned via complex molecular mechanisms that include the regulation of the glucose transporters GLUTs, mainly GLUT4 and GLUT1. Besides GLUTs, glucose can also be transported by cotransporters of the sodium-glucose cotransporter (SGLT) (SLC5 gene) family, in which SGLT1 and SMIT1 were shown to be expressed in the heart. This SGLT-mediated uptake does not seem to be directly linked to energy production but is rather associated with intracellular signalling triggering important processes such as the production of reactive oxygen species. Glucose transport is markedly affected in cardiac diseases such as cardiac hypertrophy, diabetic cardiomyopathy and heart failure. These alterations are not only fingerprints of these diseases but are involved in their onset and progression. The present review will depict the importance of glucose transport in healthy and diseased heart, as well as proposed therapies targeting glucose transporters.

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