Stimulation of mu opioid, but not GABAergic, receptors of the lateral habenula alters free feeding in rats

• Published in: Neuroscience letters Vol. 771; p. 136417
• Main Authors: Carlson, Hannah N., Christensen, Brooke A., Pratt, Wayne E.
• Format: Journal Article
• Language: English
• Published: Ireland Elsevier B.V 06.02.2022
• Subjects: Analgesics, Opioid - pharmacology; Animals; Baclofen; Baclofen - pharmacology; Eating; Enkephalin, Ala-MePhe-Gly- - pharmacology; Feeding; Feeding Behavior; GABA Agonists - pharmacology; Habenula - drug effects; Habenula - metabolism; Habenula - physiology; Lateral habenula; Locomotion; Male; Motivation; Muscimol; Muscimol - pharmacology; Opioid; Rats; Rats, Sprague-Dawley; Receptors, GABA - metabolism; Receptors, Opioid, mu - agonists; Receptors, Opioid, mu - metabolism; Opioid; Lateral habenula; Motivation; Muscimol; Baclofen; Feeding
• ISSN: 0304-3940; 1872-7972; 1872-7972
• DOI: 10.1016/j.neulet.2021.136417

•We investigated whether manipulation of the LHb impacts free feeding behavior.•Feeding was examined following LHb inactivation or mu-opioid receptor stimulation.•LHb baclofen/muscimol injection did not alter feeding on palatable or pabulum diets.•Temporary inactivation of the LHb increased locomotor behavior.•Mu-opioid stimulation decreased palatable intake but increased chow consumption. Overconsumption, or eating beyond the point of homeostasis, is a key feature in the development of obesity. Although people are consuming beyond the point of homeostasis, they are not consuming constantly or indefinitely. Thus, there is likely a mechanism that acts to terminate periods of food intake at some point beyond satiation and prior to aversion, or the negative effects of extreme excess (nausea, bloating, etc.). The purpose of the present study was to assess the lateral habenula as a candidate region for such a mechanism, due to its connectivity to midbrain reward circuitry, sensitivity to metabolic signaling, and pronounced role in drug-related motivated behaviors. Two groups of male Sprague-Dawley rats were surgically implanted with bilateral guide cannula targeting the LHb. Rats were then habituated to feeding chambers, wherein locomotion and food intake were monitored throughout a two-hour session. One experimental group was tested in the presence of rat chow; the second group was instead given access to a sweetened fat diet. Each subject separately received a 0.2 μL vehicle (0.9% saline solution) and baclofen-muscimol (50 ng/0.2 μL of each drug dissolved in 0.9% saline) injection. Additionally, on a third injection day, each rat received an injection of mu-opioid agonist DAMGO (0.1 μg/0.2 μL) prior to placement in the chamber. LHb inactivation did not result in significant alterations in feeding behavior, but produced a consistent increase in locomotor activity in both experimental groups. Mu-opioid receptor stimulation increased feeding on standard chow, but decreased intake of the sweetened-fat diet. Although LHb inactivation did not increase feeding as predicted, the novel finding that mu opioid receptor stimulation decreased feeding on a highly palatable diet, but increased intake of rat chow, highlights a differential role for the LHb in regulating hedonic consummatory behavior.