Transgenic expression of fatty acid transport protein 1 in the heart causes lipotoxic cardiomyopathy

Hsiu Chiang Chiu, Attila Kovacs, Robert M. Blanton, Xianlin Han, Michael Courtois, Caria J. Weinheimer, Kathryn A. Yamada, Sylvain Brunei, Haodong Xu, Jeanne M. Nerbonne, Michael J. Welch, Nicole M. Fettig, Terry L. Sharp, Nandakumar Sambandam, Krista M. Olson, Daniel S. Ory, Jean E. Schaffer

Research output: Contribution to journalArticlepeer-review

370 Scopus citations


Evidence is emerging that systemic metabolic disturbances contribute to cardiac myocyte dysfunction and clinically apparent heart failure, independent of associated coronary artery disease. To test the hypothesis that perturbation of lipid homeostasis in cardiomyocytes contributes to cardiac dysfunction, we engineered transgenic mice with cardiac-specific overexpression of fatty acid transport protein 1 (FATP1) using the α-myosin heavy chain gene promoter. Two independent transgenic lines demonstrate 4-fold increased myocardial free fatty acid (FFA) uptake that is consistent with the known function of FATP1. Increased FFA uptake in this model likely contributes to early cardiomyocyte FFA accumulation (2-fold increased) and subsequent increased cardiac FFA metabolism (2-fold). By 3 months of age, transgenic mice have echocardiographic evidence of impaired left ventricular filling and biatrial enlargement, but preserved systolic function. Doppler tissue imaging and hemodynamic studies confirm that these mice have predominantly diastolic dysfunction. Furthermore, ambulatory ECG monitoring reveals prolonged QTC intervals, reflecting reductions in the densities of repolarizing, voltage-gated K+ currents in ventricular myocytes. Our results show that in the absence of systemic metabolic disturbances, such as diabetes or hyperlipidemia, perturbation of cardiomyocyte lipid homeostasis leads to cardiac dysfunction with pathophysiological findings similar to those in diabetic cardiomyopathy. Moreover, the MHC-FATP model supports a role for FATPs in FFA import into the heart in vivo.

Original languageEnglish (US)
Pages (from-to)225-233
Number of pages9
JournalCirculation research
Issue number2
StatePublished - Feb 4 2005
Externally publishedYes


  • Cardiomyopathy
  • Lipids
  • Metabolism

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine
  • Physiology


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