Sodium-glucose co-transporters (SGLT2) inhibitors prevent lipid droplets formation in vascular inflammation or lipid overload by SGLT2-independent mechanism

This is the first report demonstrating that SGLT2-I prevent the formation of LDs in the vasculature. Empagliflozin downregulates LDs formation in vascular inflammation or lipid overload via an SGLT2-independent mechanism. Empagliflozin's protective effects involve the NHE1/PKC/NOX pathway in the TNF response but not in the OA response.

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Publication Details

Journal
Biomedicine & Pharmacotherapy
Published
2025-03-14
DOI
https://doi.org/10.1016/j.biopha.2025.117967
Citations
5
Primary Topic
Diabetes Treatment and Management
Type
article
Field-Weighted Citation Impact
6.47

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article

Sodium-glucose co-transporters (SGLT2) inhibitors prevent lipid droplets formation in vascular inflammation or lipid overload by SGLT2-independent mechanism

Kamila Wojnar‐Lason, Diane Bakker, Coert J. Zuurbier, Natalia Chorazy et al.
5 citations
Biomedicine & Pharmacotherapy
Diabetes Treatment and Management
6.47
article

Sodium-glucose co-transporters (SGLT2) inhibitors prevent lipid droplets formation in vascular inflammation or lipid overload by SGLT2-independent mechanism

Kamila Wojnar‐Lason, Diane Bakker, Coert J. Zuurbier, Natalia Chorazy, Marta Z. Pacia, Stefan Chłopicki, Anna M. Gdula
article en
5 citations

Abstract

This is the first report demonstrating that SGLT2-I prevent the formation of LDs in the vasculature. Empagliflozin downregulates LDs formation in vascular inflammation or lipid overload via an SGLT2-independent mechanism. Empagliflozin's protective effects involve the NHE1/PKC/NOX pathway in the TNF response but not in the OA response.

Biomedicine & PharmacotherapyVol. 185
Jagiellonian University (PL), Amsterdam Neuroscience (NL), University of Amsterdam (NL)
Narodowe Centrum Nauki, Narodowym Centrum Nauki
Openalex Percentile: Top 4%
Diabetes Treatment and Management
6.47
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