Empagliflozin Improves Diastolic Function in HFpEF by Restabilizing the Mitochondrial Respiratory Chain.
Circ Heart Fail
; 17(6): e011107, 2024 Jun.
Article
in En
| MEDLINE
| ID: mdl-38847102
ABSTRACT
BACKGROUND:
Clinical studies demonstrated beneficial effects of sodium-glucose-transporter 2 inhibitors on the risk of cardiovascular death in patients with heart failure with preserved ejection fraction (HFpEF). However, underlying processes for cardioprotection remain unclear. The present study focused on the impact of empagliflozin (Empa) on myocardial function in a rat model with established HFpEF and analyzed underlying molecular mechanisms.METHODS:
Obese ZSF1 (Zucker fatty and spontaneously hypertensive) rats were randomized to standard care (HFpEF, n=18) or Empa (HFpEF/Empa, n=18). ZSF1 lean rats (con, n=18) served as healthy controls. Echocardiography was performed at baseline and after 4 and 8 weeks, respectively. After 8 weeks of treatment, hemodynamics were measured invasively, mitochondrial function was assessed and myocardial tissue was collected for either molecular and histological analyses or transmission electron microscopy.RESULTS:
In HFpEF Empa significantly improved diastolic function (E/é con 17.5±2.8; HFpEF 24.4±4.6; P<0.001 versus con; HFpEF/Empa 19.4±3.2; P<0.001 versus HFpEF). This was accompanied by improved hemodynamics and calcium handling and by reduced inflammation, hypertrophy, and fibrosis. Proteomic analysis demonstrated major changes in proteins involved in mitochondrial oxidative phosphorylation. Cardiac mitochondrial respiration was significantly impaired in HFpEF but restored by Empa (Vmax complex IV con 0.18±0.07 mmol O2/s/mg; HFpEF 0.13±0.05 mmol O2/s/mg; P<0.041 versus con; HFpEF/Empa 0.21±0.05 mmol O2/s/mg; P=0.012 versus HFpEF) without alterations of mitochondrial content. The expression of cardiolipin, an essential stability/functionality-mediating phospholipid of the respiratory chain, was significantly decreased in HFpEF but reverted by Empa (con 15.9±1.7 nmol/mg protein; HFpEF 12.5±1.8 nmol/mg protein; P=0.002 versus con; HFpEF/Empa 14.5±1.8 nmol/mg protein; P=0.03 versus HFpEF). Transmission electron microscopy revealed a reduced size of mitochondria in HFpEF, which was restored by Empa.CONCLUSIONS:
The study demonstrates beneficial effects of Empa on diastolic function, hemodynamics, inflammation, and cardiac remodeling in a rat model of HFpEF. These effects were mediated by improved mitochondrial respiratory capacity due to modulated cardiolipin and improved calcium handling.Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Rats, Zucker
/
Stroke Volume
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Benzhydryl Compounds
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Diastole
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Disease Models, Animal
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Sodium-Glucose Transporter 2 Inhibitors
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Glucosides
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Heart Failure
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Mitochondria, Heart
Limits:
Animals
Language:
En
Journal:
Circ Heart Fail
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Circ. Heart fail
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Circulation. Heart failure
Journal subject:
ANGIOLOGIA
/
CARDIOLOGIA
Year:
2024
Document type:
Article
Country of publication: