4.6 Article

Projections from D2 Neurons in Different Subregions of Nucleus Accumbens Shell to Ventral Pallidum Play Distinct Roles in Reward and Aversion

期刊

NEUROSCIENCE BULLETIN
卷 37, 期 5, 页码 623-640

出版社

SPRINGER
DOI: 10.1007/s12264-021-00632-9

关键词

Nucleus accumbens shell; Ventral pallidum; D2 neurons; Reward; Aversion; Motivation

资金

  1. National Science Foundation of China [31571095, 91332122]
  2. Key Scientific Technological Innovation Research project from the Ministry of Education
  3. Insitute Guo Qiang at Tsinghua University
  4. Beijing Program on the Study of Functional Chips and Related Core Technologies of Brain-inspired Computing Systems

向作者/读者索取更多资源

The nucleus accumbens shell plays a crucial role in reward and aversion, with D2 neurons having varied effects on behavior based on their location within the NAcSh. Activation of D2 neurons in different regions of the NAcSh can induce different behaviors and affect movement speed. This study sheds light on the controversy surrounding the function of NAcSh D2 neurons and provides new insights into the heterogeneous nature of the NAcSh.
The nucleus accumbens shell (NAcSh) plays an important role in reward and aversion. Traditionally, NAc dopamine receptor 2-expressing (D2) neurons are assumed to function in aversion. However, this has been challenged by recent reports which attribute positive motivational roles to D2 neurons. Using optogenetics and multiple behavioral tasks, we found that activation of D2 neurons in the dorsomedial NAcSh drives preference and increases the motivation for rewards, whereas activation of ventral NAcSh D2 neurons induces aversion. Stimulation of D2 neurons in the ventromedial NAcSh increases movement speed and stimulation of D2 neurons in the ventrolateral NAcSh decreases movement speed. Combining retrograde tracing and in situ hybridization, we demonstrated that glutamatergic and GABAergic neurons in the ventral pallidum receive inputs differentially from the dorsomedial and ventral NAcSh. All together, these findings shed light on the controversy regarding the function of NAcSh D2 neurons, and provide new insights into understanding the heterogeneity of the NAcSh.

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