l-carnitine transports fatty acids into mitochondria function The Role of in acid transport and β -oxidation in l-carnitine transports long chain fatty

For treatment of primary systemic carnitine deficiency, a genetic impairment of normal biosynthesis or utilization of levocarnitine from dietary sources, or for the treatment of secondary carnitine deficiency resulting from an inborn error of metabolism such as glutaric aciduria II, methyl malonic aciduria, propionic acidemia, and medium chain fatty acylCoA dehydrogenase deficiency

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This selective action demonstrates sophisticated biological intelligence in gene regulation patterns

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It also counteracts the increased appetite that follows weight loss [112, 113]