Inhibitors of sodium-glucose transport protein 2: A new multidirectional therapeutic option for heart failure patients

Several mechanisms have been suggested to explain positive cardiovascular effects observed in studies with sodium-glucose co-transporter 2 (SGLT2) inhibitors. The reduction in glucose reabsorption in proximal tubuli induced by SGLT2 inhibitors increases urinary glucose and sodium excretion resulting...

Full description

Saved in:
Bibliographic Details
Published in:Cardiology journal Vol. 30; no. 1; pp. 143 - 149
Main Authors: Kubica, Jacek, Kubica, Aldona, Grzelakowska, Klaudyna, Stolarek, Wioleta, Grąbczewska, Zofia, Michalski, Piotr, Niezgoda, Piotr, Bartuś, Stanisław, Budaj, Andrzej, Dąbrowski, Mariusz, Drożdż, Jarosław, Gellert, Ryszard, Jaguszewski, Miłosz J, Jankowski, Piotr, Legutko, Jacek, Lesiak, Maciej, Leszek, Przemysław, Małyszko, Jolanta, Mitkowski, Przemysław, Nessler, Jadwiga, Pawlaczyk, Krzysztof, Siller-Matula, Jolanta, Stompór, Tomasz, Wolnik, Bogumił, Navarese, Eliano Pio
Format: Journal Article
Language:English
Published: Poland Wydawnictwo Via Medica 01-01-2023
Via Medica
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Several mechanisms have been suggested to explain positive cardiovascular effects observed in studies with sodium-glucose co-transporter 2 (SGLT2) inhibitors. The reduction in glucose reabsorption in proximal tubuli induced by SGLT2 inhibitors increases urinary glucose and sodium excretion resulting in increased osmotic diuresis and consequently in decreased plasma volume, followed by reduced preload. In addition, the hemodynamic effects of SGLT2 inhibition were observed in both hyper and euglycemic patients. Due to the complex and multidirectional effects induced by SGLT2 inhibitors, this originally antidiabetic group of drugs has been successfully used to treat patients with heart failure as well as for subjects with chronic kidney disease. Moreover, their therapeutic potential seems to be even broader than the indications studied to date.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1897-5593
1898-018X
DOI:10.5603/CJ.a2021.0133