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Inborn errors Congenital defects involve enzyme deficiencies in the carnitine transport or metabolic pathways, such as CPT II deficiency, which affects the function of the carnitine transporter CPT II and leads to impaired fatty acid -oxidation, and CACT deficiency, which affects the function of the carnitine transporter CACT and results in carnitine shuttle dysfunction

Peer-reviewed research supports its application in cognitive enhancement and neurodegenerative disease contexts

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[ ] [PMID: 26000442] Basic & Clinical pharmacology , 12th ed

The multiple actions of GLP-1 on the process of glucose-stimulated insulin secretion

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