A role for the endocannabinoid 2-arachidonoyl-sn-glycerol for social and high-fat food reward in male mice

Autor: Dandan Li, Jennifer Daglian, Kwang-Mook Jung, Don Wei, DaYeon Lee, Daniele Piomelli
Rok vydání: 2016
Předmět:
Male
0301 basic medicine
Cannabinoid receptor
medicine.medical_treatment
Monoacylglycerol lipase
Male mice
Mice
Transgenic

Hippocampus
Article
Nucleus Accumbens
Mice
Random Allocation
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
Cocaine
Receptor
Cannabinoid
CB1

Reward
Conditioning
Psychological

medicine
Animals
High-fat reward
Social Behavior
Receptor
Pharmacology
musculoskeletal
neural
and ocular physiology

Anandamide
Social reward
Dietary Fats
Endocannabinoid system
Monoacylglycerol Lipases
030104 developmental biology
nervous system
chemistry
Biochemistry
lipids (amino acids
peptides
and proteins)

Brain stimulation reward
Cannabinoid
Psychology
Neuroscience
psychological phenomena and processes
030217 neurology & neurosurgery
Endocannabinoids
Signal Transduction
Zdroj: Wei, D; Lee, D; Li, D; Daglian, J; Jung, K-M; & Piomelli, D. (2016). A role for the endocannabinoid 2-arachidonoyl-sn-glycerol for social and high-fat food reward in male mice. PSYCHOPHARMACOLOGY, 233(10), 1911-1919. doi: 10.1007/s00213-016-4222-0. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/5c38t9p2
ISSN: 1432-2072
0033-3158
DOI: 10.1007/s00213-016-4222-0
Popis: The endocannabinoid system is an important modulator of brain reward signaling. Investigations have focused on cannabinoid (CB1) receptors, because dissection of specific contributions of individual endocannabinoids has been limited by the available toolset. While we recently described an important role for the endocannabinoid anandamide in the regulation of social reward, it remains to be determined whether the other major endocannabinoid, 2-arachidonoyl-sn-glycerol (2-AG), serves a similar or different function.To study the role of 2-AG in natural reward, we used a transgenic mouse model (MGL-Tg mice) in which forebrain 2-AG levels are selectively reduced. We complemented behavioral analysis with measurements of brain 2-AG levels.We tested male MGL-Tg mice in conditioned place preference (CPP) tasks for high-fat food, social contact, and cocaine. We measured 2-AG content in the brain regions of interest by liquid chromatography/mass spectrometry.Male MGL-Tg mice are impaired in developing CPP for high-fat food and social interaction, but do develop CPP for cocaine. Furthermore, compared to isolated mice, levels of 2-AG in socially stimulated wild-type mice are higher in the nucleus accumbens and ventral hippocampus (183 and 140 % of controls, respectively), but unchanged in the medial prefrontal cortex.The results suggest that reducing 2-AG-mediated endocannabinoid signaling impairs social and high-fat food reward in male mice, and that social stimulation mobilizes 2-AG in key brain regions implicated in the control of motivated behavior. The time course of this response differentiates 2-AG from anandamide, whose role in mediating social reward was previously documented.
Databáze: OpenAIRE