Evidence map›Paper›PMID 39812105›Full record

ArticleeLife2025

Complementary cognitive roles for D2-MSNs and D1-MSNs during interval timing.

Robert A Bruce, Matthew Weber, Alexandra Bova, Rachael Volkman, Casey Jacobs, Kartik Sivakumar, Hannah Stutt, Youngcho Kim, Rodica Curtu, Nandakumar S Narayanan

Abstract read
In one paragraph

Article in eLife, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Article
  2. Glycolysis-enhancing αAlzheimer's research & therapy · 2026
    Article
  3. Article
  4. Midbrain Dopamine Warps Subjective Time via Threshold Setting But Not Clock Speed.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Robert A BruceDepartment of Neurology, University of Iowa, Iowa City, United States.
Matthew WeberDepartment of Neurology, University of Iowa, Iowa City, United States.
Alexandra BovaDepartment of Neurology, University of Iowa, Iowa City, United States.
Rachael VolkmanDepartment of Neurology, University of Iowa, Iowa City, United States.
Casey JacobsDepartment of Neurology, University of Iowa, Iowa City, United States.
Kartik SivakumarDepartment of Neurology, University of Iowa, Iowa City, United States.
Hannah StuttDepartment of Neurology, University of Iowa, Iowa City, United States.
Youngcho KimDepartment of Neurology, University of Iowa, Iowa City, United States.
Rodica CurtuDepartment of Mathematics, University of Iowa, Iowa City, United States.ORCID 0000-0003-2163-4689
Nandakumar S NarayananDepartment of Neurology, University of Iowa, Iowa City, United States.ORCID 0000-0002-0427-0003

Funding

Timing and dopamine in frontostriatal circuitsR01MH116043 · NIMH · UNIVERSITY OF IOWA · PI NARAYANAN, NANDAKUMAR · 2018 to 2022
$2.4M
NIMH NIH HHS R01 MH116043NIMH NIH HHS R01MH116043
6 · The paper itself

Abstract

The role of striatal pathways in cognitive processing is unclear. We studied dorsomedial striatal cognitive processing during interval timing, an elementary cognitive task that requires mice to estimate intervals of several seconds and involves working memory for temporal rules as well as attention to the passage of time. We harnessed optogenetic tagging to record from striatal D2-dopamine receptor-expressing medium spiny neurons (D2-MSNs) in the indirect pathway and from D1-dopamine receptor-expressing MSNs (D1-MSNs) in the direct pathway. We found that D2-MSNs and D1-MSNs exhibited distinct dynamics over temporal intervals as quantified by principal component analyses and trial-by-trial generalized linear models. MSN recordings helped construct and constrain a four-parameter drift-diffusion computational model in which MSN ensemble activity represented the accumulation of temporal evidence. This model predicted that disrupting either D2-MSNs or D1-MSNs would increase interval timing response times and alter MSN firing. In line with this prediction, we found that optogenetic inhibition or pharmacological disruption of either D2-MSNs or D1-MSNs increased interval timing response times. Pharmacologically disrupting D2-MSNs or D1-MSNs also changed MSN dynamics and degraded trial-by-trial temporal decoding. Together, our findings demonstrate that D2-MSNs and D1-MSNs had opposing dynamics yet played complementary cognitive roles, implying that striatal direct and indirect pathways work together to shape temporal control of action. These data provide novel insight into basal ganglia cognitive operations beyond movement and have implications for human striatal diseases and therapies targeting striatal pathways.

Indexed as

CognitionCorpus StriatumMedium Spiny NeuronsMemory, Short-TermModels, NeurologicalAnimalsFemaleMaleMiceOptogeneticsReceptors, Dopamine D1Receptors, Dopamine D2Time FactorsTime PerceptionReceptors, Dopamine D1Receptors, Dopamine D2dopaminemouseneurosciencestriatumtiming

Identifiers

PMID39812105
PMCPMC11735027

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.