Suppression of food intake by a complement C3a agonist [Trp5]-oryzatensin(5-9)

被引:23
|
作者
Ohinata, Kousaku [1 ]
Suetsugu, Kentaro [1 ]
Fujiwara, Yoko [1 ]
Yoshikawa, Masaaki [1 ]
机构
[1] Kyoto Univ, Grad Sch Agr, Div Food Sci & Biotechnol, Kyoto 6110011, Japan
关键词
food intake; WPLPR; complement C3a; prostaglandin E-2; EP4; receptor;
D O I
10.1016/j.peptides.2006.11.020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
[Trp(5)]-oryzatensin(5-9) (WPLPR), an agonist peptide for complement C3a. receptor, has been designed based on the C-terminal region of ileum-contracting peptide oryzatensin derived from rice protein. We previously reported that WPLPR has anti-analgesic and anti-amnesic activities after central or oral administration. In this study, we found a novel function of WPLPR on food intake. WPLPR suppressed food intake after intracerebroventricular or intraperitoneal (i.p.) administration at a dose of 3-30 nmol/mouse or 30-300 mg/kg, respectively, in fasted mice. orally administered WPLPR at a dose of 300 mg/kg also decreased food intake. WPLPR decreased gastric emptying after i.p. injection at a dose of 300 mg/kg. The anorexigenic activity of WPLPR was blocked by cyclooxygenase inhibitor or antagonist for prostaglandin (PG) E receptor EP4 subtype. These results suggest that WPLPR decreases food intake through PGE(2) production followed by EP4 receptor activation. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:602 / 606
页数:5
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