SGLT2i and GLP1-RA exert additive cardiorenal protection with a RAS blocker in uninephrectomized db/db mice

SGLT2i 和 GLP1-RA 与 RAS 阻滞剂一起在接受单肾切除术的 db/db 小鼠中发挥附加心肾保护作用

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作者:Nerea Martos-Guillami #, Ander Vergara #, Carmen Llorens-Cebrià, Aku Enam Motto, Irene Martínez-Díaz, Francisco Gonçalves, Maria Magdalena Garcias-Ramis, Estibaliz Allo-Urzainqui, Alonso Narváez, Sheila Bermejo, Vicent Muñoz, Juan León-Román, Roser Ferrer-Costa, Conxita Jacobs-Cachá, Jordi Vilardell

Discussion

Our results suggest that the combination of SGLT2i with GLP-1RA is superior in cardiorenal protection in DKD than the drugs administered alone on top of RAS blockade.

Methods

Male and female uninephrectomized type 2 diabetic db/db mice were treated with empagliflozin and/or semaglutide on top of ramipril during 8 weeks. During the study body weight, water and food intake were weekly monitored, glycaemia biweekly and albuminuria and glomerular filtration rate (GFR) before and after the treatment. At the end of the experiment, kidney and heart were isolated for histological and gene expression studies as well as for intrarenal RAS state assessment.

Results

Semaglutide combined with ramipril and/or empagliflozin significantly decreased albuminuria but only when combined with both compounds, semaglutide further decreased blood glucose, glomerular hyperfiltration in male mice and glomerular mesangial matrix expansion. In kidney, only the triple treatment with empagliflozin, semaglutide and ramipril reduced the expression of the proinflammatory and profibrotic genes ccl2 and TGFß1. In addition, the combination of empagliflozin and semaglutide on top of RAS blockade was superior in decreasing cardiomyocyte hypertrophy and heart fibrosis in db/db mice.

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