Closing the loop on impulsivity via nucleus accumbens delta-band activity in mice and man

Something for your doctor to consider about how to treat if this area was damaged. 
http://www.pnas.org/content/early/2017/12/12/1712214114.abstract?sid=216629b2-a6c1-4a69-978b-be308e0e2f83

1. Hemmings Wu^a,¹,
2. Kai J. Miller^a,¹,
3. Zack Blumenfeld^b,
4. Nolan R. Williams^c,
5. Vinod K. Ravikumar^a,
6. Karen E. Lee^a,
7. Bina Kakusa^a,
8. Matthew D. Sacchet^c,
9. Max Wintermark^d,
10. Daniel J. Christoffel^e,
11. Brian K. Rutt^d,
12. Helen Bronte-Stewart^a,^b,
13. Brian Knutson^f,
14. Robert C. Malenka^e,², and
15. Casey H. Halpern^a,²

Author Affiliations

1. Contributed by Robert C. Malenka, November 5, 2017 (sent for review July 11, 2017; reviewed by Andre G. Machado and Sameer A. Sheth)

1. Abstract
2. Full Text
3. Authors & Info
4. Figures
5. SI
6. Metrics
7. Related Content
8. PDF
9. PDF + SI

Significance

We reveal prominent delta oscillations in the nucleus accumbens preceding food reward in mice and use them to guide responsive neurostimulation to suppress binge-like behavior. Similar electrographic signatures are observed in human nucleus accumbens during reward anticipation as well, suggesting their translational potential in the development of a treatment for loss of impulse control in obesity and perhaps additional brain disorders.

Abstract

Reward hypersensitization is a common feature of neuropsychiatric disorders, manifesting as impulsivity for anticipated incentives. Temporally specific changes in activity within the nucleus accumbens (NAc), which occur during anticipatory periods preceding consummatory behavior, represent a critical opportunity for intervention. However, no available therapy is capable of automatically sensing and therapeutically responding to this vulnerable moment in time when anticipation-related neural signals may be present. To identify translatable biomarkers for an off-the-shelf responsive neurostimulation system, we record local field potentials from the NAc of mice and a human anticipating conventional rewards. We find increased power in 1- to 4-Hz oscillations predominate during reward anticipation, which can effectively trigger neurostimulation that reduces consummatory behavior in mice sensitized to highly palatable food. Similar oscillations are present in human NAc during reward anticipation, highlighting the translational potential of our findings in the development of a treatment for a major unmet need.