Ubiquinol Supplementation Alters Exercise Induced Fatigue by Increasing Lipid Utilization in Mice

• Published in: Nutrients Vol. 11; no. 11; p. 2550
• Main Authors: Chen, Huan-Chieh, Huang, Chi-Chang, Lin, Tien-Jen, Hsu, Mei-Chich, Hsu, Yi-Ju
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 23.10.2019; MDPI
• Subjects: Adenosine triphosphate; Ammonia; AMP deaminase; Animal Feed - analysis; Animals; anti-fatigue; Antioxidants; ATP; Dietary Supplements; Drug dosages; Electron transfer; Exercise; exercise performance; Fatigue; Fatigue - prevention & control; glycogen storage; Lactic acid; Lipid Metabolism - drug effects; Lipids; Male; Medical research; Metabolism; Mice; Mice, Inbred ICR; Mitochondria; Muscle Strength - drug effects; Musculoskeletal system; Nutrition; Nutrition research; Oxidative stress; Physical Conditioning, Animal; Physical fitness; Public health; q10; Specific Pathogen-Free Organisms; Swimming; Systematic review; Ubiquinol; Ubiquinone - administration & dosage; Ubiquinone - analogs & derivatives; Ubiquinone - pharmacology; Taiwan; Q10; glycogen storage; anti-fatigue; exercise performance
• ISSN: 2072-6643; 2072-6643
• DOI: 10.3390/nu11112550

Ubiquinol (QH), a reduced form of coenzyme Q10, is a lipid antioxidant that is hydro-soluble and is commonly formulated in commercial supplements. Ubiquinol has been increasingly reported to exert antioxidant functions, in addition to its role in the cell energy-producing system of mitochondria and adenosine triphosphate (ATP) production. The aim of this study was to assess the potential beneficial effects of QH on anti-fatigue and ergogenic functions following physiological challenge. Forty 8-week-old male Institute of Cancer Research (ICR) mice were divided into four groups ( = 10 for each group): Group 1 (vehicle control or oil only); Group 2 (1X QH dose or 102.5 mg/kg); Group 3 (2X QH dose or 205 mg/kg); Group 4 (6X QH dose or 615 mg/kg). Anti-fatigue activity and exercise performance were studied using the forelimb grip strength experiment and exhaustive weight-loaded swimming time, and levels of serum lactate, ammonia, glucose, BUN (blood urea nitrogen), creatine kinase (CK), and free fatty acids (FFA) after an acute exercise challenge. The forelimb grip strength and exhaustive weight-loaded swimming time of the QH-6X group were significantly higher than those of the other groups. QH supplementation dose-dependently reduced serum lactate, ammonia, and CK levels and increased the FFA concentration after acute exercise. In addition, QH increased the liver and muscle glycogen content, an important energy source during exercise. Therefore, the results suggest that QH formulation is a safe dietary supplement for amelioration of fatigue and for promoting exercise performance.