| Literature DB >> 30609899 |
Naohisa Shobako1,2, Atsushi Ishikado1, Yutaro Ogawa1, Yoko Sono1, Takashi Kusakari1, Makoto Suwa1, Motonobu Matsumoto1, Kousaku Ohinata2.
Abstract
We recently identified a novel, potent antihypertensive peptide, Leu-Arg-Ala (LRA; minimum effective dose = 0.25 mg/kg), from rice bran protein. In this study, we found that LRA potently relaxed mesenteric arteries isolated from spontaneously hypertensive rats (SHRs) (EC50 = 0.1 μM). In contrast, the vasorelaxant activity of each amino acid that constitutes the LRA tripeptide was remarkably attenuated. The LRA-induced vasorelaxant activity was inhibited by N(G)-nitro-l-arginine methyl ester (L-NAME; NO synthase [NOS] inhibitor) but not by an antagonist of bradykinin B2 and Mas receptors or by a phosphoinositide 3-kinase inhibitor. The antihypertensive effect induced after the oral administration of LRA was inhibited by L-NAME. LRA also induced the phosphorylation of endothelial NOS in human umbilical vein endothelial cells. Taken together, LRA may exhibit antihypertensive effects via NO-mediated vasorelaxation. LRA is the first example of a NO-dependent vasorelaxant peptide identified from rice bran protein.Entities:
Keywords: NO synthesis; antihypertensive effect; novel peptide; spontaneously hypertensive rats; vasorelaxation
Mesh:
Substances:
Year: 2019 PMID: 30609899 DOI: 10.1021/acs.jafc.8b06341
Source DB: PubMed Journal: J Agric Food Chem ISSN: 0021-8561 Impact factor: 5.279