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Cell Rep. 2019 Feb 5;26(6):1389-1398.e3. doi: 10.1016/j.celrep.2019.01.044.

Activation of the Rostral Intralaminar Thalamus Drives Reinforcement through Striatal Dopamine Release.

Author information

1
Department of Pharmacology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
2
Department of Anatomy and Neurobiology, University of Maryland School of Medicine, Baltimore, MD 21201, USA; Department of Psychiatry, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
3
Department of Pharmacology, University of Maryland School of Medicine, Baltimore, MD 21201, USA. Electronic address: bmathur@som.umaryland.edu.

Abstract

Glutamatergic projections of the thalamic rostral intralaminar nuclei of the thalamus (rILN) innervate the dorsal striatum (DS) and are implicated in dopamine (DA)-dependent incubation of drug seeking. However, the mechanism by which rILN signaling modulates reward seeking and striatal DA release is unknown. We find that activation of rILN inputs to the DS drives cholinergic interneuron burst-firing behavior and DA D2 receptor-dependent post-burst pauses in cholinergic interneuron firing. In vivo, optogenetic activation of this pathway drives reinforcement in a DA D1 receptor-dependent manner, and chemogenetic suppression of the rILN reduces dopaminergic nigrostriatal terminal activity as measured by fiber photometry. Altogether, these data provide evidence that the rILN activates striatal cholinergic interneurons to enhance the pursuit of reward through local striatal DA release and introduce an additional level of complexity in our understanding of striatal DA signaling.

KEYWORDS:

Parkinson’s disease; addiction; associative thalamus; caudate; goal-directed behavior; movement; putamen

PMID:
30726725
DOI:
10.1016/j.celrep.2019.01.044
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