Department of Cardiology, Fukuoka University School of Medicine, Fukuoka, Japan.
Department of Cardiology, Fukuoka University Nishijin Hospital, Fukuoka, Japan.
J Renin Angiotensin Aldosterone Syst. 2021 Aug 4;2021:9916789. doi: 10.1155/2021/9916789. eCollection 2021.
Male apolipoprotein E-knockout mice fed a high-fat diet were divided into control (CTL), valsartan (30 mg/kg) (VAL), sacubitril (30 mg/kg) (SAC), and valsartan plus sacubitril (30 mg/kg each) (VAL/SAC) groups after 4 weeks of prefeeding and were subsequently treated for 12 weeks.
The VAL/SAC group exhibited significantly higher serum brain natriuretic peptide levels; more subtle changes in left ventricular systolic diameter, fractional shortening, and ejection fraction, and significantly higher expression levels of natriuretic peptide precursor B and markers of angiogenesis, including clusters of differentiation 34, vascular endothelial growth factor A, and monocyte chemotactic protein 1, than the CTL group.
Valsartan plus sacubitril preserved left ventricular systolic function in apolipoprotein E-knockout mice fed a high-fat diet. This result suggests that myocardial angiogenic factors induced by ARNI might provide cardioprotective effects.
雄性载脂蛋白 E 基因敲除小鼠高脂饮食喂养 4 周后进行预喂养,分为对照组(CTL)、缬沙坦(30mg/kg)(VAL)、沙库巴曲缬沙坦(30mg/kg)(SAC)和缬沙坦加沙库巴曲缬沙坦(各 30mg/kg)(VAL/SAC)组,随后治疗 12 周。
VAL/SAC 组血清脑钠肽水平明显升高;左心室收缩直径、缩短分数和射血分数变化较轻微,脑钠肽前体 B 和血管生成标志物如分化簇 34、血管内皮生长因子 A 和单核细胞趋化蛋白 1 的表达水平明显升高,与 CTL 组相比。
缬沙坦加沙库巴曲缬沙坦可改善载脂蛋白 E 基因敲除小鼠高脂饮食引起的左心室收缩功能障碍。这一结果表明,ARNI 诱导的心肌血管生成因子可能提供心脏保护作用。