Reconstituted HDL (Milano) Treatment Efficaciously Reverses Heart Failure with Preserved Ejection Fraction in Mice

Mudit Mishra, Ilayaraja Muthuramu, Joseph Pierre Aboumsallem, Herman Kempen, Bart De Geest

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

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) Milano (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% (p < 0.0001) lower myocardial capillary density and markedly (p < 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 (p < 0.01), and reduced interstitial fibrosis (p < 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 Milano reversed pathological remodeling and functional cardiac abnormalities.

Original languageEnglish
Article number3399
JournalInternational journal of molecular sciences
Volume19
Issue number11
DOIs
Publication statusPublished - 30 Oct 2018
Externally publishedYes

Keywords

  • Animals
  • Apolipoprotein A-I/pharmacology
  • Coronary Circulation/drug effects
  • Dietary Fats/adverse effects
  • Drug Combinations
  • Female
  • Heart Failure/chemically induced
  • Humans
  • Lipoproteins, HDL/pharmacology
  • Mice
  • Microcirculation/drug effects
  • Myocardium/metabolism
  • Phosphatidylcholines/pharmacology

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