Sodium-glucose cotransporter 2 inhibitors and renin-angiotensin-aldosterone system, possible cellular interactions and benefits

Sodium glucose cotransporter 2 inhibitors (SGLT2is) are a newly developed class of anti-diabetics which exert potent hypoglycemic effects in the diabetic milieu. However, the evidence suggests that they also have extra-glycemic effects. The renin-angiotensin-aldosterone system (RAAS) is a hormonal s...

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Veröffentlicht in:Cellular signalling 2024-10, Vol.122, p.111335, Article 111335
Hauptverfasser: Forouzanmehr, Behina, Hedayati, Amir Hossein, Gholami, Emad, Hemmati, Mohammad Amin, Maleki, Mina, Butler, Alexandra E., Jamialahmadi, Tannaz, Kesharwani, Prashant, Yaribeygi, Habib, Sahebkar, Amirhossein
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Sprache:eng
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Zusammenfassung:Sodium glucose cotransporter 2 inhibitors (SGLT2is) are a newly developed class of anti-diabetics which exert potent hypoglycemic effects in the diabetic milieu. However, the evidence suggests that they also have extra-glycemic effects. The renin-angiotensin-aldosterone system (RAAS) is a hormonal system widely distributed in the body that is important for water and electrolyte homeostasis as well as renal and cardiovascular function. Therefore, modulating RAAS activity is a main goal in patients, notably diabetic patients, which are at higher risk of complications involving these organ systems. Some studies have suggested that SGLT2is have modulatory effects on RAAS activity in addition to their hypoglycemic effects and, thus, these drugs can be considered as promising therapeutic agents for renal and cardiovascular disorders. However, the exact molecular interactions between SGLT2 inhibition and RAAS activity are not clearly understood. Therefore, in the current study we surveyed the literature for possible molecular mechanisms by which SGLT2is modulate RAAS activity. •Sodium glucose cotransporter 2 inhibitors (SGLT2is) are a new class of anti-diabetics.•SGLT2is exert potent hypoglycemic effects in the diabetic milieu.•We review possible molecular mechanisms by which SGLT2is modulate RAAS activity.
ISSN:0898-6568
1873-3913
1873-3913
DOI:10.1016/j.cellsig.2024.111335