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Dillmann WH

Role of bile acids in dysbiosis and treatment of nonalcoholic fatty liver disease

Pharmacologically this yields a highly selective GHS-R1a agonist which, in classical rodent studies (Raun et al., Eur J Endocrinol 1998), does not significantly elevate cortisolemia, ACTH, prolactin or FSH/LH at effective doses, unlike GHRP-2 and GHRP-6

I think right now its going to weed out the people who were never really body positive to begin with.

While Ipamorelin remains primarily a research ligand , its well-characterized mechanisms of action and relative selectivity make it a valuable tool in endocrine and pharmacological biology