Impulsive behavior is characterized as acting without forethought and lacking the ability to withold responses. Disordered impulsivity is a major feature of a number of psychiatric disorders including attention deficit hyperactivity disorder (ADHD), conduct disorder, and antisocial personality disorder, as well as binge eating and manic episodes in bipolar disorders. Pharmacological treatments for impulsive behavior are inadequate, and a limiting factor in the development of new pharmacological treatments is a lack of understanding of the neural circuits underlying impulsivity. In the proposed research, I aim to extend progress in this field by using novel transgenic and in vivo imaging tools to study the neural circuitry underlying impulsivity. My previous work shows that adult expression of the serotonin 1B receptor (5-HT1BR) on non-serotonergic cells influences the impulsive action (response inhibition) component of impulsivity. The experiments in this project aim to characterize the scope of 5-HT1BR modulation of the multiple subcomponents of impulsivity including impulsive choice (deferred gratification). Additionally, I will identify the population(s of 5-HT1BRs that contribute to impulsive behavior and define the neural circuit mechanisms. Lastly, through the use of state-of- the-art in vivo calcium imaging methods, the effect of 5-HT1BRs on nodes of the neural circuits will be measured during impulsive behaviors. These studies will serve as a foundation for translational projects investigating the neural basis of disordered impulsivity with the aim to identify targets for the development of new treatments for psychiatric disorders in which impulsivity is a key component. Additionally, this project will provide me with career mentorship as well as technical, statistical, and theoretical training to enable my transition to an independent primary investigator.

Public Health Relevance

Impulsivity is understudied but poses a substantial health and financial burden on society, and is a key component in a number of psychiatric disorders including attention deficit hyperactivity disorder, binge eating, and bipolar disorder. The serotonin 1B receptor has been implicated in regulating impulsive behavior, however, neither the neural circuits which regulate impulsivity nor the ways in which serotonin influences them are known. This project proposes to use cutting edge genetic and imaging technology to delineate the neural circuits that control impulsivity so that better pharmacological treatments may be developed.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Career Transition Award (K99)
Project #
1K99MH106731-01A1
Application #
9033589
Study Section
Special Emphasis Panel (ZMH1-ERB-M (05))
Program Officer
Desmond, Nancy L
Project Start
2015-09-21
Project End
2017-08-31
Budget Start
2015-09-21
Budget End
2016-08-31
Support Year
1
Fiscal Year
2015
Total Cost
$129,761
Indirect Cost
$8,564
Name
New York State Psychiatric Institute
Department
Type
DUNS #
167204994
City
New York
State
NY
Country
United States
Zip Code
10032
Nautiyal, Katherine M; Hen, René (2017) Serotonin receptors in depression: from A to B. F1000Res 6:123
Nautiyal, Katherine M; Wall, Melanie M; Wang, Shuai et al. (2017) Genetic and Modeling Approaches Reveal Distinct Components of Impulsive Behavior. Neuropsychopharmacology 42:1182-1191
Nautiyal, Katherine M; Okuda, Mayumi; Hen, Rene et al. (2017) Gambling disorder: an integrative review of animal and human studies. Ann N Y Acad Sci 1394:106-127
Nautiyal, Katherine M; Tritschler, Laurent; Ahmari, Susanne E et al. (2016) A Lack of Serotonin 1B Autoreceptors Results in Decreased Anxiety and Depression-Related Behaviors. Neuropsychopharmacology 41:2941-2950