» Articles » PMID: 32077851

The Hippocampus Encodes Delay and Value Information During Delay-discounting Decision Making

Overview
Journal Elife
Specialty Biology
Date 2020 Feb 21
PMID 32077851
Citations 11
Authors
Affiliations
Soon will be listed here.
Abstract

The hippocampus, a region critical for memory and spatial navigation, has been implicated in delay discounting, the decline in subjective reward value when a delay is imposed. However, how delay information is encoded in the hippocampus is poorly understood. Here, we recorded from CA1 of mice performing a delay-discounting decision-making task, where delay lengths, delay positions, and reward amounts were changed across sessions, and identified subpopulations of CA1 neurons that increased or decreased their firing rate during long delays. The activity of both delay-active and -suppressed cells reflected delay length, delay position, and reward amount; but manipulating reward amount differentially impacted the two populations, suggesting distinct roles in the valuation process. Further, genetic deletion of the N-methyl-D-aspartate (NMDA) receptor in hippocampal pyramidal cells impaired delay-discount behavior and diminished delay-dependent activity in CA1. Our results suggest that distinct subclasses of hippocampal neurons concertedly support delay-discounting decisions in a manner that is dependent on NMDA receptor function.

Citing Articles

Brain mechanisms of temporal processing in impulsivity: Relevance to attention-deficit hyperactivity disorder.

White E, Dalley J Brain Neurosci Adv. 2024; 8:23982128241272234.

PMID: 39148691 PMC: 11325328. DOI: 10.1177/23982128241272234.


The role of the human hippocampus in decision-making under uncertainty.

Attaallah B, Petitet P, Zambellas R, Toniolo S, Maio M, Ganse-Dumrath A Nat Hum Behav. 2024; 8(7):1366-1382.

PMID: 38684870 PMC: 11272595. DOI: 10.1038/s41562-024-01855-2.


Habitual intake of fat and sugar is associated with poorer memory and greater impulsivity in humans.

Yeomans M, Armitage R, Atkinson R, Francis H, Stevenson R PLoS One. 2023; 18(8):e0290308.

PMID: 37616232 PMC: 10449134. DOI: 10.1371/journal.pone.0290308.


The Hippocampus Contributes to Temporal Discounting When Delays and Rewards Are Experienced in the Moment.

Patt V, Hunsberger R, Jones D, Verfaellie M J Neurosci. 2023; 43(31):5710-5722.

PMID: 37463727 PMC: 10401634. DOI: 10.1523/JNEUROSCI.2250-22.2023.


Navigation task and action space drive the emergence of egocentric and allocentric spatial representations.

Vijayabaskaran S, Cheng S PLoS Comput Biol. 2022; 18(10):e1010320.

PMID: 36315587 PMC: 9648855. DOI: 10.1371/journal.pcbi.1010320.


References
1.
Epstein L, Dearing K, Temple J, Cavanaugh M . Food reinforcement and impulsivity in overweight children and their parents. Eat Behav. 2008; 9(3):319-27. PMC: 4682358. DOI: 10.1016/j.eatbeh.2007.10.007. View

2.
Reber T, Bausch M, Mackay S, Bostrom J, Elger C, Mormann F . Representation of abstract semantic knowledge in populations of human single neurons in the medial temporal lobe. PLoS Biol. 2019; 17(6):e3000290. PMC: 6564037. DOI: 10.1371/journal.pbio.3000290. View

3.
Olafsdottir H, Barry C, Saleem A, Hassabis D, Spiers H . Hippocampal place cells construct reward related sequences through unexplored space. Elife. 2015; 4:e06063. PMC: 4479790. DOI: 10.7554/eLife.06063. View

4.
Pfeiffer B, Foster D . Hippocampal place-cell sequences depict future paths to remembered goals. Nature. 2013; 497(7447):74-9. PMC: 3990408. DOI: 10.1038/nature12112. View

5.
Tsien J, Huerta P, Tonegawa S . The essential role of hippocampal CA1 NMDA receptor-dependent synaptic plasticity in spatial memory. Cell. 1996; 87(7):1327-38. DOI: 10.1016/s0092-8674(00)81827-9. View