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Primary vs Secondary Carnitine Deficiency Explained At a Glance Primary carnitine deficiency is a genetic disorder where a defective transporter causes the body to lose carnitine

Practical Application : particularly useful for athletes who train several times per week or in double sessions

The mitochondria in each cell function like engines, converting lipids into the energy needed for exercise

For beta oxidation of the fatty acids the molecule of fatty acid has to first be transported across the inner mitochondrial membrane and this can only occur in the presence of L-carnitine which actually binds to the fatty acids thereby permitting its movement into the mitochondria

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A preworkout dose supports plasma availability