A fatty gut feeling

被引:158
作者
Piomelli, Daniele [1 ,2 ,3 ,4 ]
机构
[1] Univ Calif Irvine, Dept Anat & Neurobiol, Irvine, CA 92612 USA
[2] Univ Calif Irvine, Dept Pharmacol, Irvine, CA 92612 USA
[3] Univ Calif Irvine, Dept Biol Chem, Irvine, CA 92612 USA
[4] Ist Italiano Tecnol, Dept Drug Discovery & Dev, I-16163 Genoa, Italy
关键词
HYDROLYZING ACID AMIDASE; FOOD-INTAKE; SMALL-INTESTINE; N-ACYLPHOSPHATIDYLETHANOLAMINE; MOLECULAR CHARACTERIZATION; GASTROINTESTINAL-TRACT; PEPTIDE-1; SECRETION; TRANSPORTER FAT; BODY-WEIGHT; OLEOYLETHANOLAMIDE;
D O I
10.1016/j.tem.2013.03.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The absorptive epithelium of the proximal small intestine converts oleic acid released during fat digestion into oleoylethanolamide (OEA), an endogenous high-affinity agonist of peroxisome proliferator-activated receptor-alpha (PPAR-alpha). OEA interacts with this receptor to cause a state of satiety characterized by prolonged inter-meal intervals and reduced feeding frequency. The two main branches of the autonomic nervous system, sympathetic and parasympathetic, contribute to this effect: the former by enabling OEA mobilization in the gut and the latter by relaying the OEA signal to brain structures, such as the hypothalamus, that are involved in feeding regulation. OEA signaling may be a key component of the physiological system devoted to the monitoring of dietary fat intake, and its dysfunction might contribute to overweight and obesity.
引用
收藏
页码:332 / 341
页数:10
相关论文
共 92 条
[61]   CD36 is important for fatty acid and cholesterol uptake by the proximal but not distal intestine [J].
Nassir, Fatiha ;
Wilson, Brody ;
Han, Xianlin ;
Gross, Richard W. ;
Abumrad, Nada A. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (27) :19493-19501
[62]   Link between Intestinal CD36 Ligand Binding and Satiety Induced by a High Protein Diet in Mice [J].
Naville, Danielle ;
Duchampt, Adeline ;
Vigier, Michele ;
Oursel, Delphine ;
Lessire, Rene ;
Poirier, Helene ;
Niot, Isabelle ;
Begeot, Martine ;
Besnard, Philippe ;
Mithieux, Gilles .
PLOS ONE, 2012, 7 (01)
[63]   Food intake is inhibited by oral oleoylethanolamide [J].
Nielsen, MJ ;
Petersen, G ;
Astrup, A ;
Hansen, HS .
JOURNAL OF LIPID RESEARCH, 2004, 45 (06) :1027-1029
[64]   Molecular characterization of a phospholipase D generating anandamide and its congeners [J].
Okamoto, Y ;
Morishita, J ;
Tsuboi, K ;
Tonai, T ;
Ueda, N .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (07) :5298-5305
[65]   Oleoylethanolamide inhibits food intake in free-feeding rats after oral administration [J].
Oveisi, F ;
Gaetani, S ;
Eng, KTP ;
Piomelli, D .
PHARMACOLOGICAL RESEARCH, 2004, 49 (05) :461-466
[66]   Deorphanization of a G protein-coupled receptor for oleoylethanolamide and its use in the discovery of small-molecule hypophagic agents [J].
Overton, HA ;
Babbs, AJ ;
Doel, SM ;
Fyfe, MCT ;
Gardner, LS ;
Griffin, G ;
Jackson, HC ;
Procter, MJ ;
Rasamison, CM ;
Tang-Christensen, M ;
Widdowson, PS ;
Williams, GM ;
Reynet, C .
CELL METABOLISM, 2006, 3 (03) :167-175
[67]   Unsaturated fatty acid regulation of peroxisome proliferator-activated receptor α activity in rat primary hepatoctes [J].
Pawar, A ;
Jump, DB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (38) :35931-35939
[68]   A transient receptor potential channel expressed in taste receptor cells [J].
Pérez, CA ;
Huang, LQ ;
Rong, MQ ;
Kozak, JA ;
Preuss, AK ;
Zhang, HL ;
Max, M ;
Margolskee, RF .
NATURE NEUROSCIENCE, 2002, 5 (11) :1169-1176
[69]   Intestinal levels of anandamide and oleoylethanolamide in food-deprived rats are regulated through their precursors [J].
Petersen, G ;
Sorensen, C ;
Schmid, PC ;
Artmann, A ;
Tang-Christensen, M ;
Hansen, SH ;
Larsen, PJ ;
Schmid, HHO ;
Hansen, HS .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2006, 1761 (02) :143-150
[70]   The molecular logic of endocannabinoid signalling [J].
Piomelli, D .
NATURE REVIEWS NEUROSCIENCE, 2003, 4 (11) :873-884