TY - JOUR
T1 - Dorsal raphe neurons signal reward through 5-HT and glutamate
AU - Liu, Zhixiang
AU - Zhou, Jingfeng
AU - Li, Yi
AU - Hu, Fei
AU - Lu, Yao
AU - Ma, Ming
AU - Feng, Qiru
AU - Zhang, Ju en
AU - Wang, Daqing
AU - Zeng, Jiawei
AU - Bao, Junhong
AU - Kim, Ji Young
AU - Chen, Zhou Feng
AU - ElMestikawy, Salah
AU - Luo, Minmin
N1 - Funding Information:
We thank Evan S. Deneris (Case Western Reserve University) for ePet1-Cre mice, K. Deisseroth (Stanford University) for AAV-DIO-ChR2-mCherry construct, D. Duan (University of Missouri) for advice on AAV virus preparation, and J. Li (Beijing Institute of Pharmacology and Toxicology) for the analysis of brain monoamine levels. M.L. is supported by grants from the China Ministry of Science and Technology 973 Program (2010CB833902 & 2012CB837700). Z.-F.C. is supported by a NIAMS grant (AR056318).
PY - 2014/3/19
Y1 - 2014/3/19
N2 - The dorsal raphe nucleus (DRN) in the midbrain is akey center for serotonin (5-hydroxytryptamine; 5-HT)-expressing neurons. Serotonergic neurons in the DRN have been theorized to encode punishment by opposing the reward signaling of dopamine neurons. Here, we show that DRN neurons encode reward, but not punishment, through 5-HT and glutamate. Optogenetic stimulation of DRN Pet-1 neurons reinforces mice to explore the stimulation-coupled spatial region, shifts sucrose preference, drives optical self-stimulation, and directs sensory discrimination learning. DRN Pet-1 neurons increase their firing activity during reward tasks, and this activation can be used to rapidly change neuronal activity patterns in the cortex. Although DRN Pet-1 neurons are often associated with 5-HT, they also release glutamate, and both neurotransmitters contribute to reward signaling. These experiments demonstrate the abilityof DRN neurons to organize reward behaviors andmight provide insights into the underlying mechanisms of learning facilitation and anhedonia treatment.
AB - The dorsal raphe nucleus (DRN) in the midbrain is akey center for serotonin (5-hydroxytryptamine; 5-HT)-expressing neurons. Serotonergic neurons in the DRN have been theorized to encode punishment by opposing the reward signaling of dopamine neurons. Here, we show that DRN neurons encode reward, but not punishment, through 5-HT and glutamate. Optogenetic stimulation of DRN Pet-1 neurons reinforces mice to explore the stimulation-coupled spatial region, shifts sucrose preference, drives optical self-stimulation, and directs sensory discrimination learning. DRN Pet-1 neurons increase their firing activity during reward tasks, and this activation can be used to rapidly change neuronal activity patterns in the cortex. Although DRN Pet-1 neurons are often associated with 5-HT, they also release glutamate, and both neurotransmitters contribute to reward signaling. These experiments demonstrate the abilityof DRN neurons to organize reward behaviors andmight provide insights into the underlying mechanisms of learning facilitation and anhedonia treatment.
UR - http://www.scopus.com/inward/record.url?scp=84896300796&partnerID=8YFLogxK
U2 - 10.1016/j.neuron.2014.02.010
DO - 10.1016/j.neuron.2014.02.010
M3 - Article
C2 - 24656254
AN - SCOPUS:84896300796
SN - 0896-6273
VL - 81
SP - 1360
EP - 1374
JO - Neuron
JF - Neuron
IS - 6
ER -