Targeting the endothelium by combining endothelin-1 antagonism and SGLT-2 inhibition: better together?

被引:1
作者
Ambery, Phil [1 ]
Greasley, Peter J. [2 ]
Menzies, Robert I. [3 ]
Brynne, Lena [4 ]
Kulkarni, Spoorthy [5 ,6 ]
Oscarsson, Jan [1 ]
Davenport, Anthony P. [6 ]
机构
[1] AstraZeneca, Cardiovasc Renal & Metab, BioPharmaceut R&D, Clin Late Dev, Gothenburg, Sweden
[2] AstraZeneca, BioPharmaceut R&D, Res & Early Dev Cardiovasc Renal & Metab, Early Clin Dev, Gothenburg, Sweden
[3] AstraZeneca, BioPharmaceut R&D, Biosci Renal Res & Early Dev, Cardiovasc Renal & Metab, Gothenburg, Sweden
[4] AstraZeneca, Cardiovasc Renal & Metab, BioPharmaceut R&D, Informat Practice Late Dev, Gothenburg, Sweden
[5] Cambridge Univ Hosp NHS Fdn Trust, Dept Clin Pharmacol & Therapeut, Cambridge CB20QQ, England
[6] Univ Cambridge, Addenbrookes Hosp, Div Expt Med & Immunotherapeut, Cambridge, England
关键词
COTRANSPORTER; 2; INHIBITORS; RECEPTOR ANTAGONIST; ALDOSTERONE; CIRRHOSIS; DAPAGLIFLOZIN; SPARSENTAN; ZIBOTENTAN; RATIONALE; EFFICACY; DISEASE;
D O I
10.1042/CS20240605
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Endothelin A and B receptors, together with sodium-glucose cotransporter-2 (SGLT-2) channels are important targets in improving endothelial function and intervention with inhibitors has been the subject of multiple mechanistic and clinical outcome trials over recent years. Notable successes include the treatment of pulmonary hypertension with endothelin receptor antagonists, and the treatment of heart failure and chronic kidney disease with SGLT-2 inhibitors. With distinct and complementary mechanisms, in this review, we explore the logic of combination therapy for a number of diseases which have endothelial dysfunction at their heart.
引用
收藏
页码:687 / 697
页数:11
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