Endocannabinoid hedonic hotspot for sensory pleasure: anandamide in nucleus accumbens shell enhances 'liking' of a sweet reward
- PMID: 17406653
- DOI: 10.1038/sj.npp.1301376
Endocannabinoid hedonic hotspot for sensory pleasure: anandamide in nucleus accumbens shell enhances 'liking' of a sweet reward
Abstract
Cannabinoid drugs such as Delta9-THC are euphoric and rewarding, and also stimulate food intake in humans and animals. Little is known about how naturally occurring endogenous brain cannabinoids mediate pleasure from food or other natural sensory rewards. The taste reactivity paradigm measures effects of brain manipulations on affective orofacial reactions to intraorally administered pleasant and unpleasant tastes. Here we tested if anandamide microinjection into medial nucleus accumbens shell enhances these affective reactions to sweet and bitter tastes in rats. Anandamide doubled the number of positive 'liking' reactions elicited by intraoral sucrose, without altering negative 'disliking' reactions to bitter quinine. Anandamide microinjections produced Fos plumes of approximately 0.02-1 mm3 volume. Plume-based maps, integrated with behavioral data, identified the medial shell of accumbens as the anatomical hotspot responsible for hedonic amplification. Anandamide produced especially intense hedonic enhancement in a roughly 1.6 mm3 'hedonic hotspot' in dorsal medial shell, where anandamide also stimulated eating behavior. These results demonstrate that endocannabinoid signals within medial accumbens shell specifically amplify the positive hedonic impact of a natural reward (though identification of the receptor specificity of this effect will require future studies). Identification of an endocannabinoid hotspot for sensory pleasure gives insight into brain mechanisms of natural reward, and may be relevant to understanding the neural effects of cannabinoid drugs of abuse and therapeutic agents.
Similar articles
-
Hedonic hot spot in nucleus accumbens shell: where do mu-opioids cause increased hedonic impact of sweetness?J Neurosci. 2005 Dec 14;25(50):11777-86. doi: 10.1523/JNEUROSCI.2329-05.2005. J Neurosci. 2005. PMID: 16354936 Free PMC article.
-
Opioid site in nucleus accumbens shell mediates eating and hedonic 'liking' for food: map based on microinjection Fos plumes.Brain Res. 2000 Apr 28;863(1-2):71-86. doi: 10.1016/s0006-8993(00)02102-8. Brain Res. 2000. PMID: 10773195
-
Orexin in Rostral Hotspot of Nucleus Accumbens Enhances Sucrose 'Liking' and Intake but Scopolamine in Caudal Shell Shifts 'Liking' Toward 'Disgust' and 'Fear'.Neuropsychopharmacology. 2016 Jul;41(8):2101-11. doi: 10.1038/npp.2016.10. Epub 2016 Jan 20. Neuropsychopharmacology. 2016. PMID: 26787120 Free PMC article.
-
Hedonic hot spots in the brain.Neuroscientist. 2006 Dec;12(6):500-11. doi: 10.1177/1073858406293154. Neuroscientist. 2006. PMID: 17079516 Review.
-
Opioid reward 'liking' and 'wanting' in the nucleus accumbens.Physiol Behav. 2008 Aug 6;94(5):675-80. doi: 10.1016/j.physbeh.2008.04.006. Epub 2008 Apr 13. Physiol Behav. 2008. PMID: 18513761 Review.
Cited by
-
Mapping brain circuits of reward and motivation: in the footsteps of Ann Kelley.Neurosci Biobehav Rev. 2013 Nov;37(9 Pt A):1919-31. doi: 10.1016/j.neubiorev.2012.12.008. Epub 2012 Dec 19. Neurosci Biobehav Rev. 2013. PMID: 23261404 Free PMC article. Review.
-
Cannabinoid CB1 Receptors in the Intestinal Epithelium Are Required for Acute Western-Diet Preferences in Mice.Nutrients. 2020 Sep 20;12(9):2874. doi: 10.3390/nu12092874. Nutrients. 2020. PMID: 32962222 Free PMC article.
-
Incentive motivation: 'wanting' roles of central amygdala circuitry.Behav Brain Res. 2021 Aug 6;411:113376. doi: 10.1016/j.bbr.2021.113376. Epub 2021 May 20. Behav Brain Res. 2021. PMID: 34023307 Free PMC article. Review.
-
Decreased reward sensitivity in rats from the Fischer344 strain compared to Wistar rats is paralleled by differences in endocannabinoid signaling.PLoS One. 2012;7(2):e31169. doi: 10.1371/journal.pone.0031169. Epub 2012 Feb 8. PLoS One. 2012. PMID: 22347447 Free PMC article.
-
Inverse agonism of cannabinoid CB1 receptors potentiates LiCl-induced nausea in the conditioned gaping model in rats.Br J Pharmacol. 2010 Sep;161(2):336-49. doi: 10.1111/j.1476-5381.2010.00885.x. Br J Pharmacol. 2010. PMID: 20735419 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Miscellaneous
