{"title":"Sources of Synaptic Input to Neurons in the Nucleus Accumbens Shell That Project to the Ventral Pallidum","authors":"Shuanghong Li, Sa Li, Gilbert J. Kirouac","doi":"10.1002/cne.70081","DOIUrl":null,"url":null,"abstract":"<p>The shell of the nucleus accumbens (NAcSh) regulates motivation and reward via its dense projection to the ventral pallidum (VP). This ventral striatopallidal system has also been shown to regulate the activity of midbrain dopamine neurons and the release of dopamine in the NAcSh. The present study applied monosynaptic rabies tracing in the rat to quantify the brain-wide sources of synaptic input to neurons in the medial NAcSh that project to the ventromedial VP. The ventral subiculum of the hippocampus (vSub) was the largest source of input cells to the NAcSh-VP projection neurons. Anterograde tracing of vSub-NAcSh projection neurons demonstrated that their fibers terminated densely in the NAcSh largely avoiding other regions of the striatum. Another relatively strong source of input cells included the anterior part of the paraventricular nucleus of the thalamus (aPVT). The CA1, lateral septal nucleus, VP, paratenial thalamic nucleus, bed nucleus of the stria terminalis, lateral preoptic area and dorsomedial nucleus of the hypothalamus were moderately strong sources of input neurons. The prefrontal cortex, amygdala, and the basolateral nucleus of the amygdala were found to be relatively weak sources of input. A lack of sex differences for all the sources of input identified indicates that there is no apparent sexual dimorphism in the afferents to the striatopallidal system. In summary, the vSub and the aPVT are the major sources of cortical and thalamic monosynaptic inputs to the NAcSh-VP projection neurons where these inputs converge to regulate behavior and dopamine release in the NAcSh.</p>","PeriodicalId":15552,"journal":{"name":"Journal of Comparative Neurology","volume":"533 8","pages":""},"PeriodicalIF":2.1000,"publicationDate":"2025-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cne.70081","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Comparative Neurology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cne.70081","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
The shell of the nucleus accumbens (NAcSh) regulates motivation and reward via its dense projection to the ventral pallidum (VP). This ventral striatopallidal system has also been shown to regulate the activity of midbrain dopamine neurons and the release of dopamine in the NAcSh. The present study applied monosynaptic rabies tracing in the rat to quantify the brain-wide sources of synaptic input to neurons in the medial NAcSh that project to the ventromedial VP. The ventral subiculum of the hippocampus (vSub) was the largest source of input cells to the NAcSh-VP projection neurons. Anterograde tracing of vSub-NAcSh projection neurons demonstrated that their fibers terminated densely in the NAcSh largely avoiding other regions of the striatum. Another relatively strong source of input cells included the anterior part of the paraventricular nucleus of the thalamus (aPVT). The CA1, lateral septal nucleus, VP, paratenial thalamic nucleus, bed nucleus of the stria terminalis, lateral preoptic area and dorsomedial nucleus of the hypothalamus were moderately strong sources of input neurons. The prefrontal cortex, amygdala, and the basolateral nucleus of the amygdala were found to be relatively weak sources of input. A lack of sex differences for all the sources of input identified indicates that there is no apparent sexual dimorphism in the afferents to the striatopallidal system. In summary, the vSub and the aPVT are the major sources of cortical and thalamic monosynaptic inputs to the NAcSh-VP projection neurons where these inputs converge to regulate behavior and dopamine release in the NAcSh.
期刊介绍:
Established in 1891, JCN is the oldest continually published basic neuroscience journal. Historically, as the name suggests, the journal focused on a comparison among species to uncover the intricacies of how the brain functions. In modern times, this research is called systems neuroscience where animal models are used to mimic core cognitive processes with the ultimate goal of understanding neural circuits and connections that give rise to behavioral patterns and different neural states.
Research published in JCN covers all species from invertebrates to humans, and the reports inform the readers about the function and organization of nervous systems in species with an emphasis on the way that species adaptations inform about the function or organization of the nervous systems, rather than on their evolution per se.
JCN publishes primary research articles and critical commentaries and review-type articles offering expert insight in to cutting edge research in the field of systems neuroscience; a complete list of contribution types is given in the Author Guidelines. For primary research contributions, only full-length investigative reports are desired; the journal does not accept short communications.