Document Type
Article
Abstract
Obesity, by any standard, is a global health crisis. Both genetic and dietary contributions to the development and maintenance of obesity were integral factors of our experimental design. As mutations of the melanocortin 4 receptors (MC4R) are the leading monogenetic cause of obesity, MC4R haploinsufficient rats were fed a range of dietary fat (0–12 %) in a longitudinal design. Physiological and motivational assessments were performed using a locomotor task, a 5-choice sucrose preference task, an operant task with fixed and progressive ratios, as well as a distraction operant task. Dendritic spine morphology of medium spiny neurons (MSNs) of the nucleus accumbens (NAc), cells with ample D1 and D2 receptors, was also assessed. The percentage of lipid deposits in the liver of each rat was also analyzed using the Area Fraction Fractionator probe for stereological measurements. MC4R haploinsufficiency resulted in a phenotypic resemblance for adult-onset obesity that was exacerbated by the consumption of a high-fat diet. Results from the operant tasks indicate that motivational deficits due to MC4R haploinsufficiency were apparent prior to the onset of obesity and exacerbated by dietary fat consumption after obesity was well established. Moreover, MSN morphology shifted to longer spines with smaller head diameters for the MC4R+/− animals under the high-fat diet, suggesting a potential mechanism for the dysregulation of motivation to work for food. Increasing our knowledge of the neural circuitry/mechanisms responsible for the rewarding properties of food has significant implications for understanding energy balance and the development of obesity.
Digital Object Identifier (DOI)
Publication Info
Published in NeuroImmune Pharmacology and Therapeutics, Volume 3, Issue 3-4, 2024.
Rights
©2024 the author(s), published by De Gruyter. This work is licensed under the Creative Commons Attribution 4.0 International License.
APA Citation
Steiner, A. M., Roscoe, R. F., Booze, R. M., & Mactutus, C. F. (2024). Motivational dysregulation with melanocortin 4 receptor haploinsufficiency. NeuroImmune Pharmacology and Therapeutics, 3(3-4), 237–250. https://doi.org/10.1515/nipt-2024-0011