期刊
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
卷 115, 期 45, 页码 E10730-E10739出版社
NATL ACAD SCIENCES
DOI: 10.1073/pnas.1811664115
关键词
dopamine receptor; impulsivity; central amygdala; neural circuit; optogenetics
资金
- National Research Foundation of Korea - Ministry of Science, Information and Communication Technology, and Future Planning of the Republic of Korea [2013M3C7A1056101, 2013M3A9D5072550, 2016M3A9D5A01952412, 2014R1A2A2A01003337, NRF-2017R1A2B4008875, 2015R1A5A1009024, WCI 2009-003]
- Singapore Ministry of Education [MOE2015-T2-2-095]
Impulsivity is closely associated with addictive disorders, and changes in the brain dopamine system have been proposed to affect impulse control in reward-related behaviors. However, the central neural pathways through which the dopamine system controls impulsive behavior are still unclear. We found that the absence of the D2 dopamine receptor (D2R) increased impulsive behavior in mice, whereas restoration of D2R expression specifically in the central amygdala (CeA)of D2R knockout mice (Drd2(-/-)) normalized their enhanced impulsivity. Inhibitory synaptic output from D2R-expressing neurons in the CeA underlies modulation of impulsive behavior because optogenetic activation of D2R-positive inhibitory neurons that project from the CeA to the bed nucleus of the stria terminalis (BNST) attenuate such behavior. Our identification of the key contribution of D2R-expressing neurons in the CeA. BNST circuit to the control of impulsive behavior reveals a pathway that could serve as a target for approaches to the management of neuropsychiatric disorders associated with impulsivity.
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