The role of C-terminal part of ghrelin in pharmacokinetic profile and biological activity in rats.

2011 
Abstract Ghrelin is an endogenous ligand for growth hormone secretagogue receptor 1a (GHS-R1a), and consists of 28 amino acid residues with octanoyl modification at Ser 3 . The previous studies have revealed that N-terminal part of ghrelin including modified Ser 3 is the active core for the activation of GHS-R1a. On the other hand, the role of C-terminal (8–28) region in ghrelin has not been clarified yet. In the present study, we prepared human ghrelin, C-terminal truncated ghrelin derivatives and anamorelin, a small molecular GHS compound which supposedly mimics the N-terminal active core, and examined GHS-R1a agonist activity in vitro , pharmacokinetic (PK) profile and growth hormone (GH) releasing activity in rats. All compounds demonstrated potent GHS-R1a agonist activities in vitro . Although the lack of C-terminal two amino acids did not modify PK profile and GH releasing activity, the deletion of C-terminal 8 and 20 amino acids affected them, and ghrelin(1–7)-Lys-NH 2 exhibited very short plasma half-life and low GH releasing activity in vivo . In rat plasma, ghrelin(1–7)-Lys-NH 2 was degraded more rapidly than ghrelin, suggesting that C-terminal part of ghrelin protected octanoylation of Ser 3 from plasma esterases. Subdiaphragmatic vagotomy significantly attenuated GH response to ghrelin but not to anamorelin. These results suggest that the C-terminal part of ghrelin has an important role in the biological activity in vivo . We also found that ghrelin stimulated GH release mainly via a vagal nerve pathway but anamorelin augmented GH release possibly by directly acting on brain in rats.
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