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Less-selective compounds in the same class (GHRP-2, GHRP-6, hexarelin) cross-activate other endocrine axes alongside GH, which makes them noisier reference tools when researchers want to isolate ghrelin-pathway signalling from confounding hormonal effects

Higher doses (2000 mg/day) likely saturate hepatic OCTN2 transporters and elevate intracellular carnitine sufficiently to activate CPT1-mediated fatty acid oxidation

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In comparison with the control group, the data obtained in Fig

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