Empagliflozin attenuated Angiotensin II-induced left ventricular dysfunction, microvascular rarefaction, and endothelial-to-mesenchymal transition via the PI3K/AKT/eNOS signaling pathway.
Does empagliflozin improve Ang II-induced left ventricular dysfunction and microvascular rarefaction in mice and CMECs?
Empagliflozin protects against Ang II-induced left ventricular dysfunction and microvascular rarefaction by suppressing EndoMT via PI3K/AKT/eNOS signaling.
BACKGROUND: The SGLT2 inhibitor empagliflozin (EMPA) has been found to reduce the combined risk of cardiovascular death or hospitalization for heart failure in patients with or without reduced left ventricular ejection fraction, irrespective of diabetes status. The underlying mechanisms remain to be elucidated. Endothelial-to-mesenchymal transition (EndoMT) has been reported to play a pivotal role in the microvascular rarefaction. This study aimed to evaluate the effect of EMPA on angiotensin II (Ang II)-induced left ventricular dysfunction and to explore the underlying mechanism. METHODS: In vivo, C57BL/6J mice were infused with saline or Ang II (1.5 mg/kg/day) and subsequently treated with or without EMPA (10 mg/kg) for 2 weeks. mRNA sequencing and gene set enrichment analysis (GSEA) indicated that the PI3K/AKT/eNOS signalling pathway may mediate the protective effects of empagliflozin in heart failure with preserved ejection fraction (HFpEF). Finally, in vitro, PI-103 was used to treat cells, and immunofluorescence, western blotting, qPCR, and other methods were used to verify whether empagliflozin exerts its effects through the PI3K/AKT/eNOS pathway. RESULTS: In vivo, the mice treated with Ang II exhibited left ventricular dysfunction, increased microvascular rarefaction, and EndoMT, all of which were attenuated by EMPA treatment. In vitro, primary cardiac microvascular endothelial cells (CMECs) exposed to Ang II showed increased EndoMT, which was significantly inhibited by EMPA. EMPA also reversed the downregulation of PI3K/AKT/eNOS signalling and nitric oxide (NO) levels. PI-103 abrogated the anti-EndoMT effects of EMPA in CMECs. CONCLUSIONS: Our study suggested that EMPA can protect against Ang II-induced left ventricular dysfunction and microvascular rarefaction by suppressing EndoMT via PI3K/AKT/eNOS signalling.
Shen et al. (Fri,) conducted a other in Angiotensin II-induced left ventricular diastolic dysfunction. Empagliflozin vs. Saline or Angiotensin II without Empagliflozin was evaluated on Left ventricular dysfunction, microvascular rarefaction, and endothelial-to-mesenchymal transition (EndoMT). Empagliflozin attenuated Angiotensin II-induced left ventricular dysfunction, microvascular rarefaction, and endothelial-to-mesenchymal transition via the PI3K/AKT/eNOS signaling pathway.