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Moreover, LC can potentially up-regulate SOD, glutathione-peroxidase (GSH-Px), catalase (CAT), and glutathione reductase (GR) through the pathway of regulating some transcriptional factors such as nuclear-factor-erythroid-2-related-factor-2 (Nrf2), PPAR-, PPAR-, and NF-B

Plasma Membrane Carnitine Transporter Defect

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Primary Carnitine Deficiency: This is a genetically inherited disorder characterized by a disrupted carnitine metabolism

Horgan, (2020)