Triheptanoin Alleviates Ventricular Hypertrophy and Improves Myocardial Glucose Oxidation in Rats With Pressure Overload

• Published in: Journal of cardiac failure Vol. 21; no. 11; pp. 906 - 915
• Main Authors: Nguyen, T. Dung, MD, Shingu, Yasushige, MD, Amorim, Paulo A., MD, Schwarzer, Michael, PhD, Doenst, Torsten, MD
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01-11-2015
• Subjects: Analysis of Variance; anaplerosis; Animals; cardiac hypertrophy; cardiac metabolism; Cardiovascular; Disease Models, Animal; Echocardiography, Doppler; Glucose - metabolism; Hypertrophy, Left Ventricular - diagnostic imaging; Hypertrophy, Left Ventricular - drug therapy; Male; Myocardial Contraction - drug effects; Myocardial Contraction - physiology; Myocardium - metabolism; Oxidation-Reduction - drug effects; Random Allocation; Rats; Rats, Sprague-Dawley; Recovery of Function; Reference Values; Treatment Outcome; Triglycerides - administration & dosage; Triheptanoin; Triheptanoin; cardiac hypertrophy; cardiac metabolism; anaplerosis
• ISSN: 1071-9164; 1532-8414
• DOI: 10.1016/j.cardfail.2015.07.009

Abstract Objective Cardiac hypertrophy is characterized by changes in substrate utilization and activity of the Krebs cycle. We assessed the effects of triheptanoin, an odd-chain fat that might support the Krebs cycle, on cardiac metabolism and function in a model of cardiac hypertrophy. Methods and Results Rats were subjected to aortic banding (AoB) to induce pressure overload (PO). Starting at 1 week after AoB, rats were blindly fed a control diet or a special diet containing triheptanoin at 7% (T7 group) or 30% (T30 group) of total energy value. Six weeks after AoB, echocardiography revealed attenuated hypertrophy and improved diastolic function of the left ventricle. Isolated working heart perfusion showed similar cardiac power, fatty acid oxidation, substrate preference, and insulin response among groups. However, cardiac glucose oxidation (GO) was increased in the T30 group compared with the T7 and control groups. Blood levels of the odd-chain ketone body beta-hydroxypentanoate confirmed adequate bioavailability of triheptanoin. Importantly, they were directly proportional to cardiac GO. Conclusions Treatment with triheptanoin-enriched diet reduces ventricular hypertrophy and improves diastolic function in rats with PO, which is associated with enhanced cardiac GO. The results suggest targeting supplementation of the Krebs cycle to approach ventricular and metabolic remodeling in cardiac hypertrophy.