Skip to main content

Main menu

  • HOME
  • CONTENT
    • Early Release
    • Featured
    • Current Issue
    • Issue Archive
    • Collections
    • Podcast
  • ALERTS
  • FOR AUTHORS
    • Information for Authors
    • Fees
    • Journal Clubs
    • eLetters
    • Submit
    • Special Collections
  • EDITORIAL BOARD
    • Editorial Board
    • ECR Advisory Board
    • Journal Staff
  • ABOUT
    • Overview
    • Advertise
    • For the Media
    • Rights and Permissions
    • Privacy Policy
    • Feedback
    • Accessibility
  • SUBSCRIBE

User menu

  • Log out
  • Log in
  • My Cart

Search

  • Advanced search
Journal of Neuroscience
  • Log out
  • Log in
  • My Cart
Journal of Neuroscience

Advanced Search

Submit a Manuscript
  • HOME
  • CONTENT
    • Early Release
    • Featured
    • Current Issue
    • Issue Archive
    • Collections
    • Podcast
  • ALERTS
  • FOR AUTHORS
    • Information for Authors
    • Fees
    • Journal Clubs
    • eLetters
    • Submit
    • Special Collections
  • EDITORIAL BOARD
    • Editorial Board
    • ECR Advisory Board
    • Journal Staff
  • ABOUT
    • Overview
    • Advertise
    • For the Media
    • Rights and Permissions
    • Privacy Policy
    • Feedback
    • Accessibility
  • SUBSCRIBE
PreviousNext
Articles, Systems/Circuits

The Organization of Prefrontal-Subthalamic Inputs in Primates Provides an Anatomical Substrate for Both Functional Specificity and Integration: Implications for Basal Ganglia Models and Deep Brain Stimulation

William I. A. Haynes and Suzanne N. Haber
Journal of Neuroscience 13 March 2013, 33 (11) 4804-4814; https://doi.org/10.1523/JNEUROSCI.4674-12.2013
William I. A. Haynes
1Department of Pharmacology and Physiology, University of Rochester School of Medicine and Dentistry, Rochester, New York 14642 and
2Centre de Recherche de l'Institut du Cerveau et de la Moelle Epiniere (CRICM), Inserm U 975, CNRS 7225, UPMC, 75013 Paris, France
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Suzanne N. Haber
1Department of Pharmacology and Physiology, University of Rochester School of Medicine and Dentistry, Rochester, New York 14642 and
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • Article
  • Figures & Data
  • Info & Metrics
  • eLetters
  • PDF
Loading

Article Figures & Data

Figures

  • Figure 1.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 1.

    Ventral pallidal connections to the STN. A, Coronal section illustrating VP terminal fields at the edge of the medial STN border, extending medially into the hypothalamus following an injection in the subcommissural ventral pallidum (inset). B, A coronal section illustrating labeled cells (and terminals) at the edge of the medial STN border, extending medially into the hypothalamus after an injection that includes the ventral pallidum. AC, Anterior commissure; Cd, caudate nucleus; MB, mammillary body; Pu, putamen; SN, substantia nigra; STN, subthalamic nucleus; Thal, thalamus.

  • Figure 2.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 2.

    Schematic of the STN divisions. The STN was divided into thirds along the rostrocaudal axis, the rostral and caudal poles were considered as additional, distinct entities as they had specific properties. The medial tip also had specific properties and was isolated from the medial half.

  • Figure 3.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 3.

    Photomicrographs of STN labeling after cortical injections of anterograde tracers (dark field microscopy of coronal sections). A, Projections from OFC are mostly located medial to the STN′s conventional boundaries (solid white line), but are contained within the STN′s limits according to Dejerine (dashed white lines). B, Projections from vmPFC straddle the conventional medial boundary of the STN (white line). C, The dense projection from dACC is concentrated in the medial tip of the STN and is in a position to overlap with the vmPFC projection (B). It also extends beyond the medial boundary, creating a potential interface with OFC projections (A). D, The projection from area 9 is located in the medial half of the STN. Although the dense projection does not occupy the medial tip, diffuse projections do, providing an interface with dACC (C). This is visible in E, a micrograph from the same case at a higher magnification (the white arrows in D and E indicate the same blood vessel). F, Projections from the rostral area 6 are more caudal and somewhat more dorsal than DPFC projections. Nonetheless, DPFC and area 6 projections overlap extensively. This is demonstrated in G the same section as F at a higher magnification, and in H the section adjacent to F and G, showing the result of a DPFC injection in the same monkey. Matching blood vessels in F–H are indicated by the white arrows. Lesser intensity of staining in H is likely the result of variations in transport (see Results). I, Projections from M1 are dorsal and lateral. Scale bars, 200 μm.

  • Figure 4.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 4.

    Charts of frontal projections to the STN. Three coronal sections, evenly spaced along the rostrocaudal axis, are illustrated in the left panel of the figure to indicate the approximate anterior (AP = 11.10), central (AP = 10.2), and posterior thirds (AP = 9.0) levels depicted for each case (A–G). Scale bar, 5 mm. The schematic for the injection sites illustrate the center of the injection. Photographs of the prefrontal injection sites complement the prefrontal cases schematics to illustrate the extent of the halo around the injection sites. A, Projections from the vmPFC/OFC (red) are mainly outside of the conventional medial borders of the STN, and concentrated in the anterior third. B, Projections from the dACC (orange) are concentrated in the medial tip of the STN and extend over its medial border. C, D, Projections from DPFC (areas 9 and 46, respectively) (yellow) lie in the medial half of the STN, dorsal and lateral to projections from dACC (B). E, Projections from the rostral area 6 (green) appear caudally to other PFC projections, lateral but overlapping with area 46 dense projections (D). F, Projections from caudal area 6 (green) are located in the ventrolateral STN. G, Projections from M1 (blue) occupy the dorsolateral STN and seem to overlap primarily with caudal area 6 dense projections. Scale bar: (left, bottom) A–G, 1 mm. SN, Substantia nigra; STN, subthalamic nucleus; ZI, zona incerta.

  • Figure 5.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 5.

    Overlap of dense projections. A–C, Coronal view at anterior (A), central (B), and posterior (C) thirds of the 3D model. Approximate AP levels are similar to those in Fig. 3. Colored meshes represent the outer surface of the combined dense projections from each cortical area. Overlaps occur mainly between projections from functionally close cortical regions. D, Axial, superior view of the same dense projections. Scale bar, 1 mm.

  • Figure 6.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 6.

    Overlap of diffuse projections. Posterior, coronal 3D views of diffuse and dense cortical projections. Colored volumes/surfaces, Dense projection fields; colored lines, diffuse projections. A, All diffuse projections. The topography is the same as for dense projections, although there is more overlap. B, All dense projections (surfaces). Note, compared to the diffuse projections in A, the dense terminal fields show less overlap. C, Diffuse and dense projections from prefrontal areas, vmPFC, ACC, and DPFC. Diffuse projections increase the interface between the different prefrontal inputs. D, Diffuse and dense projections from premotor and motor regions. E, Diffuse projections derived from DPFC and dACC injections extend into area 6 and M1 territory, thus increasing their interface. F, Reciprocally, area 6 diffuse projections extend into the prefrontal projection territory. They are also able to interface with diffuse projections from vmPFC/OFC. Scale bar, 1 mm.

  • Figure 7.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 7.

    Passing fibers. A, Passing fibers have a topographic organization similar to diffuse projections (Fig. 6A). B, Fibers from vmPFC, OFC, and dACC travel in the medial tip of the STN and in the adjacent lateral hypothalamus. C, Fibers from DPFC travel in the medial half of the STN. D, Fibers from rostral and caudal area 6 travel, respectively, in the medial and lateral halves of the STN. Fibers from M1 travel in the dorsal portion of the lateral half. E–G, Views of the anterior, central, and posterior thirds of the STN illustrate the rostrocaudal topography of passing fibers. Prefrontal fibers enter the STN rostrally (E) to those from area 6 and M1 (F). However, fibers from area 6 and M1 travel further caudally (G). Scale bar, 1 mm.

Back to top

In this issue

The Journal of Neuroscience: 33 (11)
Journal of Neuroscience
Vol. 33, Issue 11
13 Mar 2013
  • Table of Contents
  • Table of Contents (PDF)
  • About the Cover
  • Index by author
  • Advertising (PDF)
  • Ed Board (PDF)
Email

Thank you for sharing this Journal of Neuroscience article.

NOTE: We request your email address only to inform the recipient that it was you who recommended this article, and that it is not junk mail. We do not retain these email addresses.

Enter multiple addresses on separate lines or separate them with commas.
The Organization of Prefrontal-Subthalamic Inputs in Primates Provides an Anatomical Substrate for Both Functional Specificity and Integration: Implications for Basal Ganglia Models and Deep Brain Stimulation
(Your Name) has forwarded a page to you from Journal of Neuroscience
(Your Name) thought you would be interested in this article in Journal of Neuroscience.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Print
View Full Page PDF
Citation Tools
The Organization of Prefrontal-Subthalamic Inputs in Primates Provides an Anatomical Substrate for Both Functional Specificity and Integration: Implications for Basal Ganglia Models and Deep Brain Stimulation
William I. A. Haynes, Suzanne N. Haber
Journal of Neuroscience 13 March 2013, 33 (11) 4804-4814; DOI: 10.1523/JNEUROSCI.4674-12.2013

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Respond to this article
Request Permissions
Share
The Organization of Prefrontal-Subthalamic Inputs in Primates Provides an Anatomical Substrate for Both Functional Specificity and Integration: Implications for Basal Ganglia Models and Deep Brain Stimulation
William I. A. Haynes, Suzanne N. Haber
Journal of Neuroscience 13 March 2013, 33 (11) 4804-4814; DOI: 10.1523/JNEUROSCI.4674-12.2013
Twitter logo Facebook logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One

Jump to section

  • Article
    • Abstract
    • Introduction
    • Materials and Methods
    • Results
    • Discussion
    • Footnotes
    • References
  • Figures & Data
  • Info & Metrics
  • eLetters
  • PDF

Responses to this article

Respond to this article

Jump to comment:

No eLetters have been published for this article.

Related Articles

Cited By...

More in this TOC Section

Articles

  • Memory Retrieval Has a Dynamic Influence on the Maintenance Mechanisms That Are Sensitive to ζ-Inhibitory Peptide (ZIP)
  • Neurophysiological Evidence for a Cortical Contribution to the Wakefulness-Related Drive to Breathe Explaining Hypocapnia-Resistant Ventilation in Humans
  • Monomeric Alpha-Synuclein Exerts a Physiological Role on Brain ATP Synthase
Show more Articles

Systems/Circuits

  • Effects of short-term synaptic plasticity in feedforward inhibitory circuits on cerebellar responses to repetitive sensory input
  • Chemogenetic Inhibition and Optogenetic Depotentiation of the Prelimbic Cortex to Paraventricular Thalamus Pathway Attenuate Abstinence-Induced Plasticity and Heroin Seeking in Rats
  • Pathway-Specific Ultrastructure of Thalamocortical Synapses in Mouse Somatosensory Area S2
Show more Systems/Circuits
  • Home
  • Alerts
  • Follow SFN on BlueSky
  • Visit Society for Neuroscience on Facebook
  • Follow Society for Neuroscience on Twitter
  • Follow Society for Neuroscience on LinkedIn
  • Visit Society for Neuroscience on Youtube
  • Follow our RSS feeds

Content

  • Early Release
  • Current Issue
  • Issue Archive
  • Collections

Information

  • For Authors
  • For Advertisers
  • For the Media
  • For Subscribers

About

  • About the Journal
  • Editorial Board
  • Privacy Notice
  • Contact
  • Accessibility
(JNeurosci logo)
(SfN logo)

Copyright © 2025 by the Society for Neuroscience.
JNeurosci Online ISSN: 1529-2401

The ideas and opinions expressed in JNeurosci do not necessarily reflect those of SfN or the JNeurosci Editorial Board. Publication of an advertisement or other product mention in JNeurosci should not be construed as an endorsement of the manufacturer’s claims. SfN does not assume any responsibility for any injury and/or damage to persons or property arising from or related to any use of any material contained in JNeurosci.