Empagliflozin and renal sodium-hydrogen exchange in healthy subjects
Source : https://academic.oup.com/jcem/advance-article/doi/10.1210/clinem/dgad088/7041118?login=false
AbstractContext. Sodium glucose co-transporter-2 inhibitors (SGLT2i) exert clinically relevant cardiorenal protection. Among several mechanisms, inhibition of t
Conclusions: In healthy young volunteers, empagliflozin acutely increases urinary pH while inducing a substrate shift towards lipid utilization and ketogenesis, without significant changes in renal NHE3 protein expression.
Combining Three Independent Pathological Stressors Induces a Heart Failure with Preserved Ejection Fraction Phenotype - PubMed
Source : https://pubmed.ncbi.nlm.nih.gov/36763506/
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Conclusions: The 3-Hit mouse model induced a reliable HFpEF phenotype with CM hypertrophy, cardiac fibrosis, and increased M2 macrophage population. This model could be used for identifying and preclinical testing of novel therapeutic strategies.
Empagliflozin suppressed cardiac fibrogenesis through sodium-hydrogen exchanger inhibition and modulation of the calcium homeostasis - Cardiovascular Diabetology
Source : https://cardiab.biomedcentral.com/articles/10.1186/s12933-023-01756-0
Background The novel sodium-glucose co-transporter 2 inhibitor (SGLT2i) potentially ameliorates heart failure and reduces cardiac arrhythmia. Cardiac fibrosis plays a pivotal role in the pathophysiology of HF and atrial myopathy,...
Conclusions: By inhibiting NHE, empagliflozin decreases the expression of phosphorylated PLC and IP3 production, thereby reducing ER Ca2 release, extracellular Ca2 entry and the profibrotic activities of atrial fibroblasts.
Empagliflozin in Adults with Chronic Kidney Disease (CKD): Current Evidence and Place in Therapy
Hyperfiltration is the driving force that leads nephrons to glomerulosclerosis and eventually results in chronic kidney disease (CKD) and end-stage kidney disease (ESKD). It has therefore been intuitive that decreasing...
Conclusion: Empagliflozin is the latest SGLT2i drug to show proven benefits in both hyperglycemia, CV disease, heart failure, and now CKD progression. The new EMPA-KIDNEY data proves that it provides benefits in patients with and without diabetes and can be used in those with eGFR down to 20 mL/min/1.73m2. The medication is further solidified...
Conclusions and Relevance: In this study, among patients with HFpEF and pacemakers, treatment with a moderately accelerated, personalized pacing rate was safe and improved quality of life, NT-proBNP levels, physical activity, and atrial fibrillation compared with the usual 60 bpm setting.