Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Role of Hippocampus in Memory01:19

Role of Hippocampus in Memory

2.2K
The hippocampus, a critical brain structure, plays an essential role in memory processing, particularly in the formation and retrieval of memory. This small, seahorse-shaped region is located within the medial temporal lobe, with one hippocampus in each brain hemisphere. Experimental studies involving lesions in the hippocampi of rats have demonstrated significant impairments in tasks such as object recognition and maze navigation, indicating the hippocampus involvement in both recognition and...
2.2K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

A neural framework for the origin of meaning: network dynamics, context and the hippocampus.

Philosophical transactions of the Royal Society of London. Series B, Biological sciences·2026
Same author

Hippocampus-evoked polysynaptic responses in the medial prefrontal cortex are attenuated in aged rats.

bioRxiv : the preprint server for biology·2026
Same author

An Operant-based Touchscreen Morph Discrimination Task Does Not Detect Age-related Mnemonic Similarity Deficits in Rats.

bioRxiv : the preprint server for biology·2026
Same author

Implications for Health Assessments of the Relationship Between Body Fat Percent and Body Condition Scoring in Fisher 344 x Brown Norway Rats Varying by Sex and Age.

Laboratory animal science professional·2026
Same author

Age-related differences in spatial memory occur alongside reduced visual fMRI BOLD but preserved viewpoint-specific scene representations.

bioRxiv : the preprint server for biology·2026
Same author

Paired associates learning performance in rats requires the nucleus reuniens.

Behavioral neuroscience·2026

Related Experiment Video

Updated: Apr 21, 2026

Acute Mouse Brain Slicing to Investigate Spontaneous Hippocampal Network Activity
07:58

Acute Mouse Brain Slicing to Investigate Spontaneous Hippocampal Network Activity

Published on: August 28, 2020

10.6K

Back to the future: preserved hippocampal network activity during reverse ambulation.

Andrew P Maurer1, Adam W Lester2, Sara N Burke1

  • 1Evelyn F. McKnight Brain Institute, Arizona Research Laboratories Division of Neural Systems, Memory and Aging, and Department of Neuroscience, College of Medicine, University of Florida, Gainesville, Florida 32611.

The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|November 8, 2014
PubMed
Summary

The study found that hippocampal place-field sequences are maintained even when rodents run backward, suggesting posterior parietal cortex involvement in updating spatial representations. This challenges head-direction-based models for sequence updating during movement.

Keywords:
oscillationsphase precessionplace cellspopulation vectorsequence learningtheta

More Related Videos

Investigations on Alterations of Hippocampal Circuit Function Following Mild Traumatic Brain Injury
10:59

Investigations on Alterations of Hippocampal Circuit Function Following Mild Traumatic Brain Injury

Published on: November 19, 2012

16.0K
Motor and Hippocampal Dependent Spatial Learning and Reference Memory Assessment in a Transgenic Rat Model of Alzheimer's Disease with Stroke
09:45

Motor and Hippocampal Dependent Spatial Learning and Reference Memory Assessment in a Transgenic Rat Model of Alzheimer's Disease with Stroke

Published on: March 22, 2016

10.9K

Related Experiment Videos

Last Updated: Apr 21, 2026

Acute Mouse Brain Slicing to Investigate Spontaneous Hippocampal Network Activity
07:58

Acute Mouse Brain Slicing to Investigate Spontaneous Hippocampal Network Activity

Published on: August 28, 2020

10.6K
Investigations on Alterations of Hippocampal Circuit Function Following Mild Traumatic Brain Injury
10:59

Investigations on Alterations of Hippocampal Circuit Function Following Mild Traumatic Brain Injury

Published on: November 19, 2012

16.0K
Motor and Hippocampal Dependent Spatial Learning and Reference Memory Assessment in a Transgenic Rat Model of Alzheimer's Disease with Stroke
09:45

Motor and Hippocampal Dependent Spatial Learning and Reference Memory Assessment in a Transgenic Rat Model of Alzheimer's Disease with Stroke

Published on: March 22, 2016

10.9K

Area of Science:

  • Neuroscience
  • Cognitive Neuroscience
  • Spatial Navigation

Background:

  • The brain's spatial navigation system relies on hippocampal place cells that activate sequentially as an animal moves.
  • The precise mechanisms for updating these sequential representations during movement, especially when direction of movement and head orientation differ, remain unclear.
  • Two primary models propose either head-direction cues or posterior parietal cortex (PPC) inputs for sequence updating.

Purpose of the Study:

  • To investigate the neural mechanisms underlying sequential place-cell activation during movement.
  • To differentiate between head-direction-based and PPC-based models of hippocampal sequence updating.
  • To examine how spatial representations are maintained when movement direction opposes head orientation.

Main Methods:

  • Rodents were trained to run both forward and backward on a linear track.
  • Electrophysiological recordings captured hippocampal place-cell activity during both running conditions.
  • Analysis focused on place-field remapping, size changes, population activity reconstruction, and theta phase precession.

Main Results:

  • Place-field activity remapped and fields increased in size during backward running compared to forward running.
  • Despite remapping, population activity accurately reconstructed the animal's location.
  • Theta phase precession, indicative of short-timescale sequence preservation, was maintained in both forward and backward running conditions.
  • Head direction did not significantly change between running conditions.

Conclusions:

  • The persistence of place-field sequences during backward running, where movement opposes head orientation, supports the role of the posterior parietal cortex in updating hippocampal activity.
  • These findings suggest that mechanisms beyond head-direction information are crucial for dynamically updating spatial sequences.
  • The study provides evidence for a partially PPC-driven mechanism for updating hippocampal spatial representations during locomotion.