Elsevier

Neuroscience

Volume 41, Issue 1, 1991, Pages 89-125
Neuroscience

Specificity in the projection patterns of accumbal core and shell in the rat

https://doi.org/10.1016/0306-4522(91)90202-YGet rights and content

Abstract

The efferent projections of the core and shell areas of the nucleus accumbens were studied with a combination of anterograde and retrograde tract-tracing methods, including Phaseolus vulgaris-leucoagglutinin, horseradish peroxidase and fluorescent tracers. Both the core and shell regions project to pallidal areas, i.e. ventral pallidum and entopeduncular nucleus, with a distinct topography in the sense that the core projection is located in the dorsolateral part of ventral pallidum, whereas the shell projects to the medial part of the subcommissural ventral pallidum. Both regions of the accumbens also project to mesencephalon with a bias for the core projection to innervate the substantia nigra-lateral mesencephalic tegmentum, and for the shell projection to reach primarily the ventral tegmental-paramedian tegmentum area. The most pronounced differences between core and shell projections exist in regard to the hypothalamus and extended amygdala. Whereas the core projects primarily to the entopeduncular nucleus including a part that invades the lateral hypothalamus, the shell, in addition, projects diffusely throughout the rostrocaudal extent of the lateral hypothalamus as well as to the extended amygdala, especially its sublenticular part.

Both the core and shell of the accumbens have unmistakable striatal characteristics both histologically and in their connectional patterns. The shell, however, has additional features that are reminiscent of the recently described extended amygdala [Alheid G. F. and Heimer L. (1988) Neuroscience27, 1–39; de Olmos J. S. et al. (1985) In The Rat Nervous System, pp. 223–334]; in fact, the possibility exists that the shell represents a transitional zone that seems to characterize most of the fringes of the striatal complex, where it adjoins the extended amygdala.

Reference (76)

  • MogensonG.J. et al.

    From motivation to action; functional interface between the limbic system and the motor system

    Prog. Neurobiol.

    (1980)
  • NautaW.J.H. et al.

    Efferent connections and nigral afferents of the nucleus accumbens septi in the rat

    Neuroscience

    (1978)
  • NielsenE.B. et al.

    Cueing effects of amphetamine and LSD; elicitation by direct microinjection of the drugs into the nucleus accumbens

    Eur. J. Pharmac.

    (1986)
  • PowellE.W. et al.

    Connections of the nucleus accumbens

    Brain Res.

    (1976)
  • SchmuedL.C. et al.

    Fluoro-Gold, a new fluorescent retrograde axonal tracer with numerous unique properties

    Brain Res.

    (1986)
  • SmithY. et al.

    Differential connections of caudate nucleus and putamen in the squirrel monkey (Saimiri sciureus)

    Neuroscience

    (1986)
  • SwansonL.W. et al.

    A note on the connections and development of the nucleus accumbens

    Brain Res.

    (1975)
  • TroianoR. et al.

    Efferent connections of the basal forebrain in the cat; the nucleus accumbens

    Expl Neurol.

    (1978)
  • Van der KooyD. et al.

    The organization of the efferent projections and striatal afferents of the entopeduncular nucleus and adjacent areas in the rat

    Brain Res.

    (1981)
  • VoornP. et al.

    Increase of enkephalin and decrease of substance P immunoreactivity in the dorsal and ventral striatum of the rat after midbrain 6-hydroxydopamine lesions

    Brain Res.

    (1987)
  • WilliamsD.J. et al.

    The efferent projections of the nucleus accumbens in the rat

    Brain Res.

    (1977)
  • WilsonC.J. et al.

    Dual topographic representation of neostriatum in the globus pallidus of rats

    Brain Res.

    (1982)
  • WiseR.A.

    The role of reward pathways in the development of drug dependence

    Pharmac. Ther.

    (1987)
  • WoodD.M. et al.

    Mediation in the nucleus accumbens of the discriminative stimulus produced by cocaine

    Pharmac. Biochem. Behav.

    (1989)
  • WouterloodF.G. et al.

    Neuroanatomical tracing by use of Phaseolus vulgaris-leucoagglutinin (PHA-L); electron microscopy of PHA-L filled neuronal somata, dendrites, and axon terminals

    Brain Res.

    (1985)
  • YoshikawaT. et al.

    Regional heterogeneity with the nucleus accumbens concerning the effects of dopaminergic agents on the content of cholecystokinin

    Neurochem. Int.

    (1989)
  • Za´borszkyL. et al.

    Cholecystokinin innervation of the ventral striatum; a morphological and radioimmunological study

    Neuroscience

    (1985)
  • ZahmD.S.

    The ventral striatopallidal parts of the basal ganglia in the rat. II. Compartmentation of ventral pallidal efferents

    Neuroscience

    (1989)
  • ZahmD.S. et al.

    Synaptic contacts of ventral striatal cells in the olfactory tubercle; correlated light and electron microscopy of anterogradely transported Phaseolus vulgaris-leucoagglutinin (PHA-L)

    Neurosci. Lett.

    (1985)
  • ZahmD.S. et al.

    Evidence for the coexistence of glutamate decar☐ylase and met-enkephalin immunoreactivities in axon terminals of rat ventral pallidum

    Brain Res.

    (1985)
  • AlexanderG.E. et al.

    Parallel organization of functionally segregated circuits linking basal ganglia and cortex

    A. Rev. Neurosci.

    (1986)
  • AlheidG.F. et al.

    Accumbens projections to dorsal and ventral pallidum and to the extended amygdala in the monkey using PHA-L

    Soc. Neurosci. Abstr.

    (1989)
  • BrockhausH.

    Aus feineren Anatomie des Septum und des Striatum

    J. Psychiat. Neurol.

    (1942)
  • ChangH.T. et al.

    Single neostriatal efferent axons in the globus pallidus; a light and electron microscopic study

    Science

    (1981)
  • ChronisterR.B. et al.

    Nucleus accumbens in historical perspective

  • de OlmosJ.S.

    The amygdaloid projection field in the rat as studied with the cupric-silver method

  • de OlmosJ. et al.

    The afferent connections of the main and the accessory olfactory bulb formations in the rat; an experimental HRP study

    J. comp. Neurol.

    (1978)
  • de OlmosJ.S. et al.

    Amygdala

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