Centre for Molecular and Vascular Biology, Department of Cardiovascular Sciences, Catholic University of Leuven, 3000 Leuven, Belgium.
The Medicines Company (Schweiz), CH-8001 GmbH Zürich, Switzerland.
Int J Mol Sci. 2018 Oct 30;19(11):3399. doi: 10.3390/ijms19113399.
Heart failure with preserved ejection fraction (HFpEF) represents a major unmet therapeutic need. This study investigated whether feeding coconut oil (CC diet) for 26 weeks in female C57BL/6N mice induces HFpEF and evaluated the effect of reconstituted high-density lipoprotein (HDL) (MDCO-216) administration on established HFpEF. Eight intraperitoneal injections of MDCO-216 (100 mg/kg protein concentration) or of an equivalent volume of control buffer were executed with a 48-h interval starting at 26 weeks after the initiation of the diet. Feeding the CC diet for 26 weeks induced pathological left ventricular hypertrophy characterized by a 17.1% ( < 0.0001) lower myocardial capillary density and markedly ( < 0.0001) increased interstitial fibrosis compared to standard chow (SC) diet mice. Parameters of systolic and diastolic function were significantly impaired in CC diet mice resulting in a reduced stroke volume, decreased cardiac output, and impaired ventriculo-arterial coupling. However, ejection fraction was preserved. Administration of MDCO-216 in CC diet mice reduced cardiac hypertrophy, increased capillary density ( < 0.01), and reduced interstitial fibrosis ( < 0.01). MDCO-216 treatment completely normalized cardiac function, lowered myocardial acetyl-coenzyme A carboxylase levels, and decreased myocardial transforming growth factor-β1 in CC diet mice. In conclusion, the CC diet induced HFpEF. Reconstituted HDL reversed pathological remodeling and functional cardiac abnormalities.
射血分数保留的心力衰竭(HFpEF)代表着一种重大的未满足的治疗需求。本研究旨在探讨在雌性 C57BL/6N 小鼠中用椰子油(CC 饮食)喂养 26 周是否会引发 HFpEF,并评估再构成高密度脂蛋白(HDL)(MDCO-216)给药对已建立的 HFpEF 的影响。在开始饮食 26 周后,每隔 48 小时进行 8 次腹腔注射 MDCO-216(100mg/kg 蛋白浓度)或等量的对照缓冲液。用 CC 饮食喂养 26 周会导致病理性左心室肥厚,表现为心肌毛细血管密度降低 17.1%(<0.0001),间质纤维化明显增加(<0.0001),与标准饲料(SC)饮食小鼠相比。CC 饮食小鼠的收缩和舒张功能参数明显受损,导致每搏量减少、心输出量降低和心室-动脉耦联受损。然而,射血分数得到了保留。在 CC 饮食小鼠中给予 MDCO-216 可减少心脏肥大,增加毛细血管密度(<0.01),并减少间质纤维化(<0.01)。MDCO-216 治疗可完全使 CC 饮食小鼠的心脏功能正常化,降低心肌乙酰辅酶 A 羧化酶水平,并降低心肌转化生长因子-β1。总之,CC 饮食可引发 HFpEF。再构成的 HDL 可逆转病理性重塑和心脏功能异常。