作者
Margarita Suardíaz, Guillermo Estivill-Torrús, Carlos Goicoechea, Ainhoa Bilbao, Fernando Rodríguez de Fonseca
发表日期
2007/12/1
期刊
Pain
卷号
133
期号
1
页码范围
99-110
出版商
LWW
简介
Oleoylethanolamide (OEA) is a natural fatty acid amide that mainly modulates feeding and energy homeostasis by binding to peroxisome proliferator-activated receptor-alpha (PPAR-α)[Rodríguez de Fonseca F, Navarro M, Gómez R, Escuredo L, Navas F, Fu J, et al. An anorexic lipid mediator regulated by feeding. Nature 2001; 414: 209–12; Fu J, Gaetani S, Oveisi F, Lo Verme J, Serrano A, Rodríguez de Fonseca F, et al. Oleoylethanolamide regulates feeding and body weight through activation of the nuclear receptor PPAR-α. Nature 2003; 425: 90–3]. Additionally, it has been proposed that OEA could act via other receptors, including the vanilloid receptor (TRPV1)[Wang X, Miyares RL, Ahern GP. Oleoylethanolamide excites vagal sensory neurones, induces visceral pain and reduces short-term food intake in mice via capsaicin receptor TRPV1. J Physiol 2005; 564: 541–7.] or the GPR119 receptor [Overton HA …
引用总数
2008200920102011201220132014201520162017201820192020202120222023202481383118151312710813121442
学术搜索中的文章