| Literature DB >> 28649756 |
Hayato Aoki1, Junya Nakato1, Takafumi Mizushige1,2, Hiroshi Iwakura3, Masaru Sato4, Hideyuki Suzuki4, Ryuhei Kanamoto1, Kousaku Ohinata1.
Abstract
Ghrelin, an endogenous peptide isolated from the stomach, is known to stimulate food intake after peripheral administration. We found that the enzymatic digest of β-lactoglobulin decreases ghrelin secretion from the ghrelin-producing cell line MGN3-1. The peptides present in the digest were comprehensively analyzed using the nanoLC-OrbitrapMS. Among them, we identified that the nonapeptide LIVTQTMKG, corresponding to β-lactoglobulin(1-9), suppresses ghrelin secretion from MGN3-1 cells. We named LIVTQTMKG 'lacto-ghrestatin'. We found that lacto-ghrestatin decreases intracellular cAMP levels and mRNA expression levels of ghrelin production-related genes in MGN3-1 cells. Orally administered lacto-ghrestatin decreases plasma ghrelin levels and food intake in fasted mice. Lacto-ghrestatin is the first food-derived peptide to suppress ghrelin secretion in vitro and in vivo.Entities:
Keywords: comprehensive analysis; food intake; ghrelin; peptide; β-lactoglobulin
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Year: 2017 PMID: 28649756 DOI: 10.1002/1873-3468.12731
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124