Inhibition of Sodium Glucose Cotransporters Improves Cardiac Performance.
cardiac metabolism
heart failure
ischemia reperfusion injury
sodium-glucose cotransporter
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
04 Jul 2019
04 Jul 2019
Historique:
received:
14
06
2019
revised:
01
07
2019
accepted:
02
07
2019
entrez:
7
7
2019
pubmed:
7
7
2019
medline:
18
12
2019
Statut:
epublish
Résumé
The sodium-glucose cotransporter (SGLT) inhibitors represent a new alternative for treating patients with diabetes mellitus. They act primarily by inhibiting glucose reabsorption in the renal tubule and therefore, decreasing blood glucose levels. While little is yet known about SGLT subtype 1, SGLT2 inhibitors have demonstrated to significantly reduce cardiovascular mortality and heart failure hospitalizations. This cardioprotective benefit seems to be independent of their glucose-lowering properties; however, the underlying mechanism(s) remains still unclear and numerous hypotheses have been postulated to date. Moreover, preclinical research has suggested an important role of SGLT1 receptors on myocardial ischemia. Following acute phase of cardiac injury there is an increased activity of SGLT1 cotransport that ensures adequate energy supply to the cardiac cells. Nonetheless, a long-term upregulation of this receptor may not be that beneficial and whether its inhibition is positive or not should be further addressed. This review aims to present the most cutting-edge insights into SGLT receptors.
Identifiants
pubmed: 31277431
pii: ijms20133289
doi: 10.3390/ijms20133289
pmc: PMC6651487
pii:
doi:
Substances chimiques
Sodium-Glucose Transport Proteins
0
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
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