Drugs of abuse hijack a mesolimbic pathway that processes homeostatic need

Author:

Tan Bowen1ORCID,Browne Caleb J.23ORCID,Nöbauer Tobias4ORCID,Vaziri Alipasha45ORCID,Friedman Jeffrey M.1ORCID,Nestler Eric J.2ORCID

Affiliation:

1. Laboratory of Molecular Genetics, Howard Hughes Medical Institute, The Rockefeller University, New York, NY 10065, USA.

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

3. Brain Health Imaging Centre, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, ON M5T 1R8, Canada.

4. Laboratory of Neurotechnology and Biophysics, The Rockefeller University, New York, NY 10065, USA.

5. The Kavli Neural Systems Institute, The Rockefeller University, New York, NY 10065, USA.

Abstract

Drugs of abuse are thought to promote addiction in part by “hijacking” brain reward systems, but the underlying mechanisms remain undefined. Using whole-brain FOS mapping and in vivo single-neuron calcium imaging, we found that drugs of abuse augment dopaminoceptive ensemble activity in the nucleus accumbens (NAc) and disorganize overlapping ensemble responses to natural rewards in a cell type–specific manner. Combining FOS-Seq, CRISPR-perturbation, and single-nucleus RNA sequencing, we identified Rheb as a molecular substrate that regulates cell type–specific signal transduction in NAc while enabling drugs to suppress natural reward consumption. Mapping NAc-projecting regions activated by drugs of abuse revealed input-specific effects on natural reward consumption. These findings characterize the dynamic, molecular and circuit basis of a common reward pathway, wherein drugs of abuse interfere with the fulfillment of innate needs.

Publisher

American Association for the Advancement of Science (AAAS)

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