Skip to main content

Umbrella menu

  • SfN.org
  • eNeuro
  • The Journal of Neuroscience
  • Neuronline
  • BrainFacts.org

Main menu

  • HOME
  • CONTENT
    • Early Release
    • Current Issue
    • Issue Archive
    • Video Archive
    • Collections
  • ALERTS
  • FOR AUTHORS
    • Preparing a Manuscript
    • Submission Guidelines
    • Fees
    • Journal Club
    • eLetters
    • Submit
  • EDITORIAL BOARD
  • ABOUT
    • Overview
    • Subscriptions
    • Advertise
    • For the Media
    • Permissions
    • Privacy Policy
    • Feedback
  • SfN.org
  • eNeuro
  • The Journal of Neuroscience
  • Neuronline
  • BrainFacts.org

User menu

  • Log in
  • Subscribe
  • My alerts

Search

  • Advanced search
Journal of Neuroscience
  • Log in
  • Subscribe
  • My alerts
Journal of Neuroscience

Advanced Search

Submit a Manuscript
  • HOME
  • CONTENT
    • Early Release
    • Current Issue
    • Issue Archive
    • Video Archive
    • Collections
  • ALERTS
  • FOR AUTHORS
    • Preparing a Manuscript
    • Submission Guidelines
    • Fees
    • Journal Club
    • eLetters
    • Submit
  • EDITORIAL BOARD
  • ABOUT
    • Overview
    • Subscriptions
    • Advertise
    • For the Media
    • Permissions
    • Privacy Policy
    • Feedback
PreviousNext
Research Articles, Behavioral/Cognitive

The Rhesus Monkey Hippocampus Critically Contributes to Scene Memory Retrieval, But Not New Learning

Sean Froudist-Walsh, Philip G.F. Browning, Paula L. Croxson, Kathy L. Murphy, Jul Lea Shamy, Tess L. Veuthey, Charles R.E. Wilson and Mark G. Baxter
Journal of Neuroscience 5 September 2018, 38 (36) 7800-7808; DOI: https://doi.org/10.1523/JNEUROSCI.0832-18.2018
Sean Froudist-Walsh
1Glickenhaus Laboratory of Neuropsychology, Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, New York 10029 and
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for Sean Froudist-Walsh
Philip G.F. Browning
1Glickenhaus Laboratory of Neuropsychology, Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, New York 10029 and
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Paula L. Croxson
1Glickenhaus Laboratory of Neuropsychology, Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, New York 10029 and
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Kathy L. Murphy
1Glickenhaus Laboratory of Neuropsychology, Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, New York 10029 and
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Jul Lea Shamy
1Glickenhaus Laboratory of Neuropsychology, Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, New York 10029 and
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Tess L. Veuthey
1Glickenhaus Laboratory of Neuropsychology, Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, New York 10029 and
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Charles R.E. Wilson
2Univ Lyon, Université Claude Bernard Lyon 1, Inserm, Stem Cell and Brain Research Institute U1208, 69500 Bron, France
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for Charles R.E. Wilson
Mark G. Baxter
1Glickenhaus Laboratory of Neuropsychology, Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, New York 10029 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

Abstract

Humans can recall a large number of memories years after the initial events. Patients with amnesia often have lesions to the hippocampus, but human lesions are imprecise, making it difficult to identify the anatomy underlying memory impairments. Rodent studies enable great precision in hippocampal manipulations, but not investigation of many interleaved memories. Thus it is not known how lesions restricted to the hippocampus affect the retrieval of multiple sequentially encoded memories. Furthermore, disagreement exists as to whether hippocampal inactivations lead to temporally graded or ungraded amnesia, which could be a consequence of differences between rodent and human studies. In the current study, rhesus monkeys of both sexes received either bilateral neurotoxic hippocampal lesions or remained unoperated controls and were tested on recognition and new learning of visual object-in-place scenes. Monkeys with hippocampal lesions were significantly impaired at remembering scenes that were encoded before the lesion. We did not observe any temporal gradient effect of the lesion on memory recognition, with recent and remote memories being equally affected by the lesion. Monkeys with hippocampal lesions showed no deficits in learning new scenes. Thus, the hippocampus, like other cortical regions, may be engaged in the acquisition and storage of new memories, but the role of the damaged hippocampus can be taken over by spared hippocampal tissue or extra-hippocampal regions following a lesion. These findings illustrate the utility of experimental paradigms for studying retrograde and anterograde amnesia that make use of the capacity of nonhuman primates to rapidly acquire many distinct visual memories.

SIGNIFICANCE STATEMENT Recalling old memories, creating new memories, and the process by which memories transition from temporary to permanent storage all may rely on the hippocampus. Whether the hippocampus is necessary for encoding and retrieval of multiple related visual memories in primates is not known. Monkeys that learned many visual memory problems before precise lesions of the hippocampus were impaired at recalling those memories after hippocampal damage regardless of when the memories were formed, but could learn new memory problems at a normal rate. This suggests the hippocampus is normally vital for retrieval of complex visual memories regardless of their age, and also points to the importance of investigating mechanisms by which memories may be acquired in the presence of hippocampal damage.

  • anterograde amnesia
  • episodic
  • macaque
  • memory
  • retrograde amnesia
  • rhesus
View Full Text

Member Log In

Sign in with your SFN login

If you have an SfN.org account and DO NOT know
your username and/or password

If you DO NOT have an SfN membership

Log in through your institution

If your organization uses OpenAthens, you can log in using your OpenAthens username and password. To check if your institution is supported, please see this list. Contact your library for more details.

Pay Per Article - You may access this article (from the computer you are currently using) for 1 day for US$35.00

Regain Access - You can regain access to a recent Pay per Article purchase if your access period has not yet expired.

Back to top

In this issue

The Journal of Neuroscience: 38 (36)
Journal of Neuroscience
Vol. 38, Issue 36
5 Sep 2018
  • 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 Rhesus Monkey Hippocampus Critically Contributes to Scene Memory Retrieval, But Not New Learning
(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.
Print
View Full Page PDF
Article Alerts
Sign In to Email Alerts with your Email Address
Citation Tools
The Rhesus Monkey Hippocampus Critically Contributes to Scene Memory Retrieval, But Not New Learning
Sean Froudist-Walsh, Philip G.F. Browning, Paula L. Croxson, Kathy L. Murphy, Jul Lea Shamy, Tess L. Veuthey, Charles R.E. Wilson, Mark G. Baxter
Journal of Neuroscience 5 September 2018, 38 (36) 7800-7808; DOI: 10.1523/JNEUROSCI.0832-18.2018

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Respond to this article

Share
The Rhesus Monkey Hippocampus Critically Contributes to Scene Memory Retrieval, But Not New Learning
Sean Froudist-Walsh, Philip G.F. Browning, Paula L. Croxson, Kathy L. Murphy, Jul Lea Shamy, Tess L. Veuthey, Charles R.E. Wilson, Mark G. Baxter
Journal of Neuroscience 5 September 2018, 38 (36) 7800-7808; DOI: 10.1523/JNEUROSCI.0832-18.2018
del.icio.us logo Digg logo Reddit logo Twitter logo CiteULike logo Facebook logo Google 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

Keywords

  • anterograde amnesia
  • episodic
  • macaque
  • memory
  • retrograde amnesia
  • rhesus

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

Research Articles

  • Regulation of myelination by exosome associated retinoic acid release from NG2-positive cells
  • Post-encoding Amygdala-Visuosensory Coupling Is Associated with Negative Memory Bias in Healthy Young Adults
  • Neural Mechanisms of Emotion Regulation Moderate the Predictive Value of Affective and Value-Related Brain Responses to Persuasive Messages
Show more Research Articles

Behavioral/Cognitive

  • Regulation of myelination by exosome associated retinoic acid release from NG2-positive cells
  • Post-encoding Amygdala-Visuosensory Coupling Is Associated with Negative Memory Bias in Healthy Young Adults
  • Neural Mechanisms of Emotion Regulation Moderate the Predictive Value of Affective and Value-Related Brain Responses to Persuasive Messages
Show more Behavioral/Cognitive
  • Home
  • Alerts
  • 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 Policy
  • Contact
  • Feedback
(JNeurosci logo)
(SfN logo)

Copyright © 2019 by the Society for Neuroscience.

JNeurosci   Print ISSN: 0270-6474   Online ISSN: 1529-2401