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It is also used to treat certain metabolic disorders (mitochondrial disorders and fatty acid oxidation disorders)

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Its pharmacological signature potent GHS-R1a-mediated GH release with negligible off-target stimulation of cortisol, prolactin, or ACTH at research-relevant concentrations makes it the ghrelin receptor agonist of choice for investigators requiring isolated GHS-pathway activation without confounding neuroendocrine variables

doi: 10.21873/anticanres.16079

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