Hedonic eating, obesity, and addiction result from increased neuropeptide Y in the nucleus accumbens during human brain evolution

Author:

Raghanti Mary Ann12ORCID,Miller Elaine N.34ORCID,Jones Danielle N.12,Smith Heather N.12,Munger Emily L.12,Edler Melissa K.12ORCID,Phillips Kimberley A.56ORCID,Hopkins William D.7ORCID,Hof Patrick R.8ORCID,Sherwood Chet C.34ORCID,Lovejoy C. Owen12ORCID

Affiliation:

1. Department of Anthropology and School of Biomedical Sciences, Kent State University, Kent, OH 44242

2. Brain Health Research Institute, Kent State University, Kent, OH 44242

3. Department of Anthropology, The George Washington University, Washington, DC 20052

4. Center for the Advanced Study of Human Paleobiology, The George Washington University, Washington, DC 20052

5. Department of Psychology, Trinity University, San Antonio, TX 78212

6. Southwest National Primate Research Center, Texas Biomedical Research Institute, San Antonio, TX 78245

7. Department of Comparative Medicine, University of Texas MD Anderson Cancer Center, Bastrop, TX 78602

8. Nash Family Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029

Abstract

The nucleus accumbens (NAc) is central to motivation and action, exhibiting one of the highest densities of neuropeptide Y (NPY) in the brain. Within the NAc, NPY plays a role in reward and is involved in emotional behavior and in increasing alcohol and drug addiction and fat intake. Here, we examined NPY innervation and neurons of the NAc in humans and other anthropoid primates in order to determine whether there are differences among these various species that would correspond to behavioral or life history variables. We quantified NPY-immunoreactive axons and neurons in the NAc of 13 primate species, including humans, great apes, and monkeys. Our data show that the human brain is unique among primates in having denser NPY innervation within the NAc, as measured by axon length density to neuron density, even after accounting for brain size. Combined with our previous finding of increased dopaminergic innervation in the same region, our results suggest that the neurochemical profile of the human NAc appears to have rendered our species uniquely susceptible to neurophysiological conditions such as addiction. The increase in NPY specific to the NAc may represent an adaptation that favors fat intake and contributes to an increased vulnerability to eating disorders, obesity, as well as alcohol and drug dependence. Along with our findings for dopamine, these deeply rooted structural attributes of the human brain are likely to have emerged early in the human clade, laying the groundwork for later brain expansion and the development of cognitive and behavioral specializations.

Funder

NSF | Directorate for Social, Behavioral and Economic Sciences

NSF | SBE | Division of Behavioral and Cognitive Sciences

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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