Marczak Ewa D, Ohinata Kousaku, Lipkowski Andrzej W, Yoshikawa Masaaki
Division of Food Science and Biotechnology, Graduate School of Agriculture, Kyoto University, Gokasho Uji, Kyoto 611-0011, Japan.
Peptides. 2006 Sep;27(9):2065-8. doi: 10.1016/j.peptides.2006.03.019. Epub 2006 May 2.
We previously reported that a bioactive tripeptide Arg-Ile-Tyr (RIY), which has been isolated as an inhibitor for angiotensin I-converting enzyme from the subtilisin digest of rapeseed protein, decreased blood pressure. In this study, we also found that RIY dose-dependently decreased food intake at a dose of 150 mg/kg after oral administration in fasted ddY male mice. The anorexigenic action of RIY was blocked by a cholecystokinin-1 CCK1 receptor antagonist, lorglumide. RIY also decreased the gastric emptying rate at a dose of 150 mg/kg and the RIY-induced delay of gastric emptying was blocked by lorglumide. However, RIY had no affinity for CCK1 receptor. Taken together, RIY decreased food intake and gastric emptying by stimulating CCK release.
我们之前报道过,一种生物活性三肽精氨酸 - 异亮氨酸 - 酪氨酸(RIY),它是从菜籽蛋白的枯草杆菌蛋白酶消化物中分离出来的血管紧张素I转换酶抑制剂,可降低血压。在本研究中,我们还发现,在禁食的ddY雄性小鼠口服给药后,RIY以150 mg/kg的剂量呈剂量依赖性地减少食物摄入量。RIY的厌食作用被胆囊收缩素 - 1(CCK1)受体拮抗剂洛谷胺阻断。RIY在150 mg/kg的剂量下也降低了胃排空率,并且RIY诱导的胃排空延迟被洛谷胺阻断。然而,RIY对CCK1受体没有亲和力。综上所述,RIY通过刺激CCK释放来减少食物摄入量和胃排空。