| Literature DB >> 24900254 |
Shinya Oishi1, Ryosuke Misu1, Kenji Tomita1, Shohei Setsuda1, Ryo Masuda1, Hiroaki Ohno1, Yousuke Naniwa2, Nahoko Ieda2, Naoko Inoue2, Satoshi Ohkura2, Yoshihisa Uenoyama2, Hiroko Tsukamura2, Kei-Ichiro Maeda2, Akira Hirasawa1, Gozoh Tsujimoto1, Nobutaka Fujii1.
Abstract
Kisspeptin is a member of the RFamide neuropeptide family that is implicated in gonadotropin secretion. Because kisspeptin-GPR54 signaling is implicated in the neuroendocrine regulation of reproduction, GPR54 ligands represent promising therapeutic agents against endocrine secretion disorders. In the present study, the selectivity profiles of GPR54 agonist peptides were investigated for several GPCRs, including RFamide receptors. Kisspeptin-10 exhibited potent binding and activation of neuropeptide FF receptors (NPFFR1 and NPFFR2). In contrast, short peptide agonists bound with much lower affinity to NPFFRs while showing relatively high selectivity toward GPR54. The possible localization of secondary kisspeptin targets was also demonstrated by variation in the levels of GnRH release from the median eminence and the type of GPR54 agonists used. Negligible affinity of the reported NPFFR ligands to GPR54 was observed and indicates the unidirectional cross-reactivity between both ligands.Entities:
Keywords: GPR54; NPFFR1, NPFFR2; Neuropeptide FF receptors; kisspeptin
Year: 2010 PMID: 24900254 PMCID: PMC4018085 DOI: 10.1021/ml1002053
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345