Evidence map›Paper›PMID 42142823›Full record

ArticleThe journal of pain2026

Effects of putative chronic pain models on locomotor activity in female and male mice.

Edna J Santos, Miriam M Fonseca, E Alfonso Romero-Sandoval, S Stevens Negus

Abstract read
In one paragraph

Article in The journal of pain, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Edna J SantosDepartment of Pharmacology & Toxicology, School of Medicine, Virginia Commonwealth University, Richmond, VA, United States.
Miriam M FonsecaDepartment of Anesthesiology, Wake Forest University School of Medicine, Winston-Salem, NC, United States.
E Alfonso Romero-SandovalDepartment of Anesthesiology, Wake Forest University School of Medicine, Winston-Salem, NC, United States.
S Stevens NegusDepartment of Pharmacology & Toxicology, School of Medicine, Virginia Commonwealth University, Richmond, VA, United States. Electronic address: sidney.negus@vcuhealth.org.

Funding

A Novel Assay to Improve Translation in Analgesic Drug DevelopmentR33NS133217 · NINDS · VIRGINIA COMMONWEALTH UNIVERSITY · PI NEGUS, SIDNEY S · 2024 to 2024
$861k
A Novel Assay to Improve Translation in Analgesic Drug DevelopmentR61NS133217 · NINDS · VIRGINIA COMMONWEALTH UNIVERSITY · PI NEGUS, SIDNEY S · 2023 to 2023
$244k
Intrinsic Efficacy as a Determinant of Opioid Effectiveness in Treatment of Pain-Depressed BehaviorF31NS122525 · NINDS · VIRGINIA COMMONWEALTH UNIVERSITY · PI EVINGTON, EDNA J · 2022 to 2023
$59k
NINDS NIH HHS F31 NS122525NINDS NIH HHS R33 NS133217NINDS NIH HHS R61 NS133217
6 · The paper itself

Abstract

Behavioral depression is a cardinal sign of clinically relevant pain and a target of pain treatment. Accordingly, preclinical assays of pain-depressed behavior can serve as tools for translational research on the expression and treatment of this key manifestation of pain. We recently validated a procedure to assess expression and pharmacological treatment of acute pain-related depression of locomotor activity produced in mice by acute treatment with intraperitoneal lactic acid (IP acid). The present study evaluated the utility of this procedure for research on locomotor depression produced by four putative models of chronic pain: (1) a model of episodic visceral pain produced by repeated daily IP acid injection, (2) a laparotomy model of postsurgical pain, (3) a cutaneous inflammatory pain model produced by intraplantar injection of complete Freund's adjuvant (Ipl CFA), and (4) a spared nerve injury (SNI) model of neuropathic pain. Locomotor activity in male and female ICR mice was objectively and quantitatively assessed in chambers with two compartments separated by a wire-mesh barrier that could be surmounted to cross between compartments. Primary dependent measures were vertical activity represented by Crosses between compartments and horizontal activity represented by the sum of photobeam breaks (Movement Counts) within each compartment. Repeated IP acid and laparotomy depressed both Crosses and Movement, and effects were alleviated by analgesics. Ipl CFA and SNI produced weak effects too small and variable to permit drug testing. These results support utility of repeated IP acid and laparotomy models for research on pain-related behavioral depression using locomotor endpoints in mice. PERSPECTIVE: Clinically relevant pain commonly produces behavioral depression. This article compared locomotor depression in mice produced by four chronic pain models. Two models (episodic visceral pain, postsurgical pain) produced locomotor depression alleviated by analgesics. Inflammatory and neuropathic pain models produced weak effects that limit their utility for research on pain-depressed behavior.

Indexed as

Chronic PainDepressionMotor ActivitySex CharacteristicsAnimalsDisease Models, AnimalFemaleFreund's AdjuvantMaleMiceMice, Inbred ICRNeuralgiaPain MeasurementVisceral PainFreund's AdjuvantInflammatory painNeuropathic painPain-depressed behaviorPostsurgical painVisceral pain

Identifiers

PMID42142823
PMCPMC13271009

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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.