4.5 Article

Dapagliflozin, sildenafil and their combination in monocrotaline-induced pulmonary arterial hypertension

期刊

BMC PULMONARY MEDICINE
卷 22, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12890-022-01939-7

关键词

Dapagliflozin; Sildenafil; Pulmonary arterial hypertension

资金

  1. National Natural Science Foundation of China [81800056]
  2. science and technology innovation program of Hunan Province [2020SK50922]
  3. Natural Science Foundation of Hunan Province [2021JJ40294]
  4. Key Research and Development Program of Hunan Province [2019SK2021]
  5. Key Project of Hunan provincial science and technology innovation [2020SK1013]

向作者/读者索取更多资源

Dapagliflozin reduces right ventricular systolic pressure and pulmonary vascular remodeling in a rat model of pulmonary arterial hypertension. However, combination therapy with dapagliflozin and sildenafil was not more effective than monotherapy with sildenafil in pulmonary arterial hypertension rats.
Background Dapagliflozin, a selective inhibitor of sodium-glucose cotransporter 2 (SGLT2), can reduce cardiovascular events and mortality in patients with heart failure. A number of mechanisms have been proposed to explain the beneficial effects of SGLT2 inhibitors. The purpose of this study was to determine whether dapagliflozin can improve pulmonary vascular remodelling and the efficacy of dapagliflozin as an add-on therapy to sildenafil in rats with pulmonary arterial hypertension (PAH). Methods A monocrotaline (MCT)-induced PAH rat model was used in our study. MCT-injected rats were randomly divided into four groups and treated for 3 weeks with daily per os treatment with vehicle, dapagliflozin (1 mg/kg/day), sildenafil (25 mg/kg/day), or a combination of dapagliflozin (1 mg/kg/day) and sildenafil (25 mg/kg/day). Haemodynamic measurements, histological analysis, enzyme-linked immunosorbent assay and western blotting analysis were employed to detect the changes in PAH rats after treatments. Results Dapagliflozin significantly attenuated MCT-induced increases in right ventricular systolic pressure (RVSP) and right ventricular hypertrophy (RVH) in PAH rats. Dapagliflozin effectively decreased the thickening of pulmonary artery media and decreased the muscularization of pulmonary arterioles in PAH rats. Moreover, dapagliflozin attenuated nucleotide-binding domain-like receptor protein 3 (NLRP3) inflammasome activation in lung tissues and the levels of interleukin-1 beta (IL-1 beta) and interleukin-18 (IL-18) in plasma. However, dapagliflozin as an add-on therapy to sildenafil in rats with PAH did not show a more pronounced beneficial effect on right ventricular systolic pressure and pulmonary vascular remodelling in MCT rats than sildenafil alone. Conclusions Dapagliflozin reduces right ventricular systolic pressure and pulmonary vascular remodelling in a rat model of PAH. However, combination therapy with dapagliflozin and sildenafil was not more effective than monotherapy with sildenafil in PAH rats.

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