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HERO ID
6469809
Reference Type
Journal Article
Subtype
Review
Title
Oleoylethanolamide: A fat ally in the fight against obesity
Author(s)
Brown, JD; Karimian Azari, E; Ayala, JE
Year
2017
Is Peer Reviewed?
1
Journal
Physiology & Behavior
ISSN:
0031-9384
EISSN:
1873-507X
Volume
176
Page Numbers
50-58
Language
English
PMID
28254531
DOI
10.1016/j.physbeh.2017.02.034
Web of Science Id
WOS:000402212000008
Abstract
Obesity is a pandemic, gateway disease that has thrived in modern, sedentary, high calorie-eating societies. Left unchecked, obesity and obesity-related diseases will continue to plague future generations with heavy burdens on economies, healthcare systems, and the quality of life of billions. There is a significant need to elucidate basic physiological mechanisms and therapies that address this global health care crisis. Oleoylethanolamide (OEA) is an endocannabinoid-like lipid that induces hypophagia and reduces fat mass in rodents. For over a decade, PPAR-α has been the most widely accepted mediator of the hypophagic action of OEA via signaling to homeostatic brain centers. Recent evidence suggests that OEA may also reduce food intake via effects on dopamine and endocannabinoid signaling within hedonic brain centers. Limited study of OEA supplementation in humans has provided some encouraging insight into OEA-based weight loss therapy, but more thorough, controlled investigations are needed. As a potential link between homeostatic and hedonic regulation of food intake, OEA is a prime starting point for the development of more effective obesity therapies.
Keywords
; brain; cannabinoids; dopamine; food intake; health services; humans; lipids; obesity; obesity-related diseases; pandemic; plague; quality of life; rodents; undereating; weight control programs/
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