» Articles » PMID: 31906370

Carnitine in Human Muscle Bioenergetics: Can Carnitine Supplementation Improve Physical Exercise?

Overview
Journal Molecules
Publisher MDPI
Specialty Biology
Date 2020 Jan 8
PMID 31906370
Citations 40
Authors
Affiliations
Soon will be listed here.
Abstract

l-Carnitine is an amino acid derivative widely known for its involvement in the transport of long-chain fatty acids into the mitochondrial matrix, where fatty acid oxidation occurs. Moreover, l-Carnitine protects the cell from acyl-CoA accretion through the generation of acylcarnitines. Circulating carnitine is mainly supplied by animal-based food products and to a lesser extent by endogenous biosynthesis in the liver and kidney. Human muscle contains high amounts of carnitine but it depends on the uptake of this compound from the bloodstream, due to muscle inability to synthesize carnitine. Mitochondrial fatty acid oxidation represents an important energy source for muscle metabolism particularly during physical exercise. However, especially during high-intensity exercise, this process seems to be limited by the mitochondrial availability of free l-carnitine. Hence, fatty acid oxidation rapidly declines, increasing exercise intensity from moderate to high. Considering the important role of fatty acids in muscle bioenergetics, and the limiting effect of free carnitine in fatty acid oxidation during endurance exercise, l-carnitine supplementation has been hypothesized to improve exercise performance. So far, the question of the role of l-carnitine supplementation on muscle performance has not definitively been clarified. Differences in exercise intensity, training or conditioning of the subjects, amount of l-carnitine administered, route and timing of administration relative to the exercise led to different experimental results. In this review, we will describe the role of l-carnitine in muscle energetics and the main causes that led to conflicting data on the use of l-carnitine as a supplement.

Citing Articles

A Comprehensive Investigation of Lipid Profile During the Solid-State Fermentation of Rice by .

Lan L, Cao Y, Yuan J, Feng R, Pan H, Mao X Foods. 2025; 14(3).

PMID: 39942130 PMC: 11817215. DOI: 10.3390/foods14030537.


Assessing the Roles of Retinol, Vitamin K2, Carnitine, and Creatine in Plant-Based Diets: A Narrative Review of Nutritional Adequacy and Health Implications.

Goldman D, Warbeck C, Barbaro R, Khambatta C, Nagra M Nutrients. 2025; 17(3).

PMID: 39940383 PMC: 11820685. DOI: 10.3390/nu17030525.


Fucoidan alleviated colitis aggravated by fiber deficiency through protecting the gut barrier, suppressing the MAPK/NF-κB pathway, and modulating gut microbiota and metabolites.

Zheng W, Tang S, Ren X, Song S, Ai C Front Nutr. 2025; 11:1462584.

PMID: 39925971 PMC: 11802440. DOI: 10.3389/fnut.2024.1462584.


H and P MR Spectroscopy to Assess Muscle Mitochondrial Dysfunction in Long COVID.

Finnigan L, Cassar M, Jafarpour M, Sultana A, Ashkir Z, Azer K Radiology. 2024; 313(3):e233173.

PMID: 39718498 PMC: 11694076. DOI: 10.1148/radiol.233173.


Habitual dietary methyl donor's intake and metabolic profile in obese individuals: a cross-sectional study.

Abdi F, Farhangi M, Mohammadzadeh M Sci Rep. 2024; 14(1):30046.

PMID: 39627237 PMC: 11615318. DOI: 10.1038/s41598-024-75388-z.


References
1.
Orer G, Guzel N . The effects of acute L-carnitine supplementation on endurance performance of athletes. J Strength Cond Res. 2013; 28(2):514-9. DOI: 10.1519/JSC.0b013e3182a76790. View

2.
Jain S, Luiken J, Snook L, Han X, Holloway G, Glatz J . Fatty acid transport and transporters in muscle are critically regulated by Akt2. FEBS Lett. 2015; 589(19 Pt B):2769-75. DOI: 10.1016/j.febslet.2015.08.010. View

3.
Jia Z, Pei Z, Maiguel D, Toomer C, Watkins P . The fatty acid transport protein (FATP) family: very long chain acyl-CoA synthetases or solute carriers?. J Mol Neurosci. 2007; 33(1):25-31. DOI: 10.1007/s12031-007-0038-z. View

4.
Cavallo A, Taurino F, Damiano F, Siculella L, Sardanelli A, Gnoni A . Acute administration of 3,5-diiodo-L-thyronine to hypothyroid rats stimulates bioenergetic parameters in liver mitochondria. J Bioenerg Biomembr. 2016; 48(5):521-529. DOI: 10.1007/s10863-016-9686-4. View

5.
Ding L, Chang M, Guo Y, Zhang L, Xue C, Yanagita T . Trimethylamine-N-oxide (TMAO)-induced atherosclerosis is associated with bile acid metabolism. Lipids Health Dis. 2018; 17(1):286. PMC: 6300890. DOI: 10.1186/s12944-018-0939-6. View