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Specifically, certain studies have investigated its capacity to upregulate growth hormone receptors (GHR), which could theoretically sensitize tissues to existing GH levels and enhance downstream anabolic processes
Are These Compounds Approved for Human Use
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
10.1016/J.BBIH.2021.100348 79 HuiC
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