Abstract

Neurons in the ventral tegmental area (VTA) that innervate the nucleus accumbens (Acb) constitute the so-called mesoaccumbens system. Increased activity by these neurons is correlated with the expectation and achievement of reward. The mesoaccumbens projection neurons are regarded as a central node in the brain networks that regulate drive and hedonic experience, and their dysregulation is a common pathophysiological step in addictive behaviors as well as major depression. Despite previous anatomical studies that have analyzed the origin of the mesoaccumbens axons within the VTA, regarded as a unit, the exact contributions of the various cytoarchitectural subdivisions of the VTA to this innervation is still unexplored; understanding these contributions would help further our understanding of their precise anatomical organization. With the aim of deciphering the contribution of the various VTA subdivisions to accumbal innervation, the present study has used retrograde tracer microinjections in the Acb to map the location within the various VTA subdivisions of neurons targeting either the shell or core compartments of the Acb in mice. Furthermore, the dopaminergic nature of these projections has also been analyzed using tyrosine-hydroxylase immunohistochemistry. We demonstrate here that small territories of the Acb core and shell are innervated simultaneously by many VTA subdivisions, contributing dopaminergic as well as non-dopaminergic axons to the accumbal innervation. In fact, single VTA subdivisions harbor both dopaminergic and non-dopaminergic neurons that project to the same accumbal territory. The most medial VTA subnuclei, like the caudal linear nucleus, project abundantly to medial aspects of the Acb core, whereas more lateral territories of the Acb are preferentially targeted by neurons located in the parabrachial pigmented and paranigral nuclei. Overall, about half of the mesoaccumbens neurons are putatively dopaminergic in mice. Anterograde single-cell labeling (Sindbis-pal-eGFP vector) of a limited sample of neurons revealed that mesoaccumbens neurons form profuse terminal arborizations to cover large volumes of either the Acb core or shell, and, unlike other VTA projection neuron populations, they do not branch to other striatal or extrastriatal structures. These anatomical observations are consistent with reports of an intense response in many Acb neurons after stimulation of very few VTA cells.

Highlights

  • The Acb is the largest component of the ventral striatum and is comprised of a dorsal core (AcbC) adjacent to the ventral CPu and a surrounding ventral shell (AcbSh) (Zaborszky et al, 1985; Voorn et al, 1989; Zahm and Brog, 1992)

  • Our results indicate that the medial aspect of the nucleus accumbens (AcbC) receives abundant projections from the midline ventral tegmental area (VTA) subdivisions interfascicular nucleus (IF), caudal linear nucleus (CLi) and rostral linear nucleus (RLi), whereas more laterally in AcbC the percentages of retrogradely labeled mesoaccumbens neurons increased at the medial aspect of parabrachial pigmented nucleus (PBP)

  • This could represent the anatomical substrate for the massive response of a high number of Acb spiny neurons after stimulation of very few VTA neurons releasing both dopamine and glutamate (Stuber et al, 2010; Yamaguchi et al, 2011). Our findings complement those described by Beier et al (2015) in mice, who reported two types of mesoaccumbens neurons depending on their pattern of collateralization in other striatal and extrastriatal targets, but did not report the existence of neurons that only projected to the Acb. This is the first anatomical study of the mouse mesoaccumbens pathway to analyze the contribution of each VTA subdivision to the innervation of the core and shell Acb subdivisions

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Summary

Introduction

The Acb is the largest component of the ventral striatum and is comprised of a dorsal core (AcbC) adjacent to the ventral CPu and a surrounding ventral shell (AcbSh) (Zaborszky et al, 1985; Voorn et al, 1989; Zahm and Brog, 1992). The AcbSh participates in conditioned aversion and enhancement to addictive drugs (Fenu et al, 2001) while the AcbC is involved in the locomotor aspect of reward learning and drug addiction (Ito et al, 2004), generating conditioned responses based on stimulus-outcome associations made by AcbSh neurons (Ikemoto, 2007), as seen in rats These processes are accomplished through a connectivity loop consisting of AcbSh projections to VTA neurons that, in turn, innervate AcbC, and this subnucleus would relay information back to more lateral VTA cells, which arborize in the CPu (Zahm, 2000; Voorn et al, 2004)

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