作者
Shinobu Takayasu, Takeshi Sakurai, Satoshi Iwasaki, Hitoshi Teranishi, Akihiro Yamanaka, S Clay Williams, Haruhisa Iguchi, Yuka Imamura Kawasawa, Yukio Ikeda, Iori Sakakibara, Kousaku Ohno, Ryoichi X Ioka, Saori Murakami, Naoshi Dohmae, Jian Xie, Toshihiro Suda, Toshiyuki Motoike, Takashi Ohuchi, Masashi Yanagisawa, Juro Sakai
发表日期
2006/5/9
期刊
Proceedings of the National Academy of Sciences
卷号
103
期号
19
页码范围
7438-7443
出版商
National Academy of Sciences
简介
Here, we report the isolation and characterization of an endogenous peptide ligand of GPR103 from rat brains. The purified peptide was found to be the 43-residue RF-amide peptide QRFP. We also describe two mouse homologues of human GPR103, termed mouse GPR103A and GPR103B. QRFP binds and activates the human GPR103, as well as mouse GPR103A and GPR103B, with nanomolar affinities in transfected cells. Systematic in situ hybridization analysis in mouse brains showed that QRFP is expressed exclusively in the periventricular and lateral hypothalamus, whereas the two receptor mRNAs are distinctly localized in various brain areas without an overlap to each other. When administered centrally in mice, QRFP induced feeding behavior, accompanied by increased general locomotor activity and metabolic rate. QRFP-induced food intake was abolished by preadministration of BIBP3226, a …
引用总数
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