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The OCTN2 carnitine transporter mediates high-affinity carnitine transport Defective OCTN2 activity reduces carnitine levels and impairs fatty acid oxidation Missense mutations in OCTN2 define the function of selected transporter domains Defects in carnitine biosynthesis do not reduce carnitine levels Acknowledgments This work was supported in part by NIH grant DK 53824

doi: 10.1053/ajkd.1998.v32.pm9708610

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Specifically, AMPK can inactivate ACC by phosphorylation, resulting in reduced activity of malonate monoacyl coenzyme A (CoA) and reducing allosteric inhibition of CPT1, thereby enhancing the activity of CPT1, which transports long-chain fatty acids from carnitine to mitochondria for -oxidation [17]

[DOI] [PMC free article] [PubMed] [Google Scholar] 86.Omori Y., Ohtani T., Sakata Y., Mano T., Takeda Y., Tamaki S., Tsukamoto Y., Kamimura D., Aizawa Y., Miwa T