Evidence map›Paper›PMID 41032042›Full record

ArticleeLife2025

Patchy striatonigral neurons modulate locomotor vigor in response to environmental valence.

Sarah Hawes, Bo Liang, Braden Oldham, Breanna T Sullivan, Lupeng Wang, Bin Song, Lisa Chang, Da-Ting Lin, Huaibin Cai

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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Whole-brain input organization ofFrontiers in neural circuits · 2026
    Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Sarah HawesTransgenic Section, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, United States.
Bo LiangIntramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore, United States.
Braden OldhamTransgenic Section, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, United States.ORCID https://orcid.org/0000-0002-4249-5502
Breanna T SullivanTransgenic Section, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, United States.
Lupeng WangTransgenic Section, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, United States.
Bin SongTransgenic Section, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, United States.
Lisa ChangTransgenic Section, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, United States.
Da-Ting LinIntramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore, United States.ORCID https://orcid.org/0000-0003-0538-7892
Huaibin CaiTransgenic Section, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, United States.ORCID https://orcid.org/0000-0002-8596-6108

Funding

In vivo imaging of dorsal striatum function in freely behaving miceZIADA000603 · NIDA · NATIONAL INSTITUTE ON DRUG ABUSE · PI LIN, DA-TING · 2015 to 2025
$22.3M
Striosomes Constrain Locomotor Vigor in Parkinson's disease and Other Movement DisordersZIAAG000959 · NIA · NATIONAL INSTITUTE ON AGING · PI CAI, HUAIBIN · 2009 to 2024
$4.0M
Intramural NIH HHS ZIA AG000959Intramural NIH HHS ZIA DA000603NIA NIH HHS ZIA AG000959NIDA NIH HHS ZIA DA000603
6 · The paper itself

Abstract

Spiny projection neurons (SPNs) in the dorsal striatum play crucial roles in locomotion control and value-based decision-making. SPNs, which include both direct-pathway striatonigral and indirect-pathway striatopallidal neurons, can be further classified into subtypes based on distinct transcriptomic profiles and cell body distribution patterns. However, how these SPN subtypes regulate spontaneous locomotion in the context of environmental valence remains unclear. Using Sepw1-Cre transgenic mice, which label a specific SPN subtype characterized by a patchy distribution of cell bodies in the dorsal striatum, we found that these patchy striatonigral neurons constrain motor vigor in response to valence differentials. In a modified light/dark box test, mice exhibited differential walking speeds between the light and dark zones. Genetic ablation of these patchy SPNs disrupted restful slowing in the dark zone and increased zone discrimination by speed. In vivo recordings linked the activity of these neurons to zone occupancy, speed, and deceleration, with a specific role in mediating deceleration. Furthermore, chemogenetic activation of patchy SPNs-and optical activation of striatonigral neurons in particular-reduced locomotion and attenuated speed-based zone discrimination. These findings reveal that a subtype of patchy striatonigral neurons regulates implicit walking speed selection based on innate valence differentials.

Indexed as

Corpus StriatumLocomotionNeuronsAnimalsMaleMiceMice, Transgenicbasal gangliadorsal striatumenvironmental valencelocomotionmouseneurosciencespiny projection neuronsstriosome

Identifiers

PMID41032042
PMCPMC12488187

What OpenQuestion holds

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Registered trials

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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.