l-Carnitine therapy improves right heart dysfunction through Cpt1-dependent fatty acid oxidation.

metabolism pulmonary arterial hypertension right heart failure

Journal

Pulmonary circulation
ISSN: 2045-8932
Titre abrégé: Pulm Circ
Pays: United States
ID NLM: 101557243

Informations de publication

Date de publication:
Jul 2022
Historique:
received: 31 01 2022
revised: 27 05 2022
accepted: 16 06 2022
entrez: 1 8 2022
pubmed: 2 8 2022
medline: 2 8 2022
Statut: epublish

Résumé

Pulmonary arterial hypertension (PAH) is a fatal vasculopathy that ultimately leads to elevated pulmonary pressure and death by right ventricular (RV) failure, which occurs in part due to decreased fatty acid oxidation and cytotoxic lipid accumulation. In this study, we tested the hypothesis that decreased fatty acid oxidation and increased lipid accumulation in the failing RV is driven, in part, by a relative carnitine deficiency. We then tested whether supplementation of l-carnitine can reverse lipotoxic RV failure through augmentation of fatty acid oxidation. In vivo in transgenic mice harboring a human BMPR2 mutation, l-carnitine supplementation reversed RV failure by increasing RV cardiac output, improving RV ejection fraction, and decreasing RV lipid accumulation through increased PPARγ expression and augmented fatty acid oxidation of long chain fatty acids. These findings were confirmed in a second model of pulmonary artery banding-induced RV dysfunction. In vitro, l-carnitine supplementation selectively increased fatty acid oxidation in mitochondria and decreased lipid accumulation through a Cpt1-dependent pathway. l-Carnitine supplementation improves right ventricular contractility in the stressed RV through augmentation of fatty acid oxidation and decreases lipid accumulation. Correction of carnitine deficiency through l-carnitine supplementation in PAH may reverse RV failure.

Identifiants

pubmed: 35911183
doi: 10.1002/pul2.12107
pii: PUL212107
pmc: PMC9326551
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e12107

Subventions

Organisme : NHLBI NIH HHS
ID : K24 HL155891
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL095797
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL146588
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL163960
Pays : United States

Informations de copyright

© 2022 The Authors. Pulmonary Circulation published by John Wiley & Sons Ltd on behalf of Pulmonary Vascular Research Institute.

Déclaration de conflit d'intérêts

V. A., E. L. B., A. R. H., and J. D. W. have all received grants from the NIH/NHLBI. V. A. has received funding from the American Heart Association, Team Phenomenal Hope Foundation, and Pulmonary Hypertension Association. A. R. H. has served as a consultant to Janssen, Complexa, GossamerBio, Bayer, United Therapeutics. A. R. H. has received funding from CMREF. A. R. H. owns stock in Tenax Thera.

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Auteurs

Vineet Agrawal (V)

Department of Medicine, Division of Cardiovascular Medicine Vanderbilt University Medical Center Nashville Tennessee USA.

Anna R Hemnes (AR)

Department of Medicine, Division of Allergy, Pulmonary, and Critical Care Medicine Vanderbilt University Medical Center Nashville Tennessee USA.

Nicholas J Shelburne (NJ)

Department of Medicine, Division of Allergy, Pulmonary, and Critical Care Medicine Vanderbilt University Medical Center Nashville Tennessee USA.

Niki Fortune (N)

Department of Medicine, Division of Allergy, Pulmonary, and Critical Care Medicine Vanderbilt University Medical Center Nashville Tennessee USA.

Julio L Fuentes (JL)

Department of Medicine, Division of Allergy, Pulmonary, and Critical Care Medicine Vanderbilt University Medical Center Nashville Tennessee USA.

Dan Colvin (D)

Vanderbilt University Institute of Imaging Vanderbilt University Nashville Tennessee USA.

Marion W Calcutt (MW)

Department of Biochemistry Vanderbilt University Nashville Tennessee USA.

Megha Talati (M)

Department of Medicine, Division of Allergy, Pulmonary, and Critical Care Medicine Vanderbilt University Medical Center Nashville Tennessee USA.

Emily Poovey (E)

Department of Medicine, Division of Allergy, Pulmonary, and Critical Care Medicine Vanderbilt University Medical Center Nashville Tennessee USA.

James D West (JD)

Department of Medicine, Division of Allergy, Pulmonary, and Critical Care Medicine Vanderbilt University Medical Center Nashville Tennessee USA.

Evan L Brittain (EL)

Department of Medicine, Division of Cardiovascular Medicine Vanderbilt University Medical Center Nashville Tennessee USA.

Classifications MeSH