Evidence map›Paper›PMID 40301473›Full record

ArticleScientific reports2025

MoSeq based 3D behavioral profiling uncovers neuropathic behavior changes in diabetic mouse model.

Akm Ashiquzzaman, Eunbin Lee, Brahnu Fentaw Znaub, An Nazmus Sakib, Geehoon Chung, Sang Seong Kim, Young Ro Kim, Hyuk-Sang Kwon, Euiheon Chung

Abstract read
In one paragraph

Article in Scientific reports, 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

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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.

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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

9 authors.

Akm Ashiquzzaman *Department of Biomedical Science and Engineering, Gwangju Institute of Science and Technology, Gwangju, South Korea.
Eunbin Lee *Department of Biomedical Science and Engineering, Gwangju Institute of Science and Technology, Gwangju, South Korea.
Brahnu Fentaw Znaub *Department of Biomedical Science and Engineering, Gwangju Institute of Science and Technology, Gwangju, South Korea.
An Nazmus SakibDepartment of Biomedical Science and Engineering, Gwangju Institute of Science and Technology, Gwangju, South Korea.
Geehoon ChungNeurogrin Inc., Seoul, South Korea.
Sang Seong KimDepartment of Biomedical Science and Engineering, Gwangju Institute of Science and Technology, Gwangju, South Korea.
Young Ro KimDepartment of Radiology, Harvard Medical School, Boston, MA, USA.
Hyuk-Sang KwonDepartment of Biomedical Science and Engineering, Gwangju Institute of Science and Technology, Gwangju, South Korea. hyuksang@gist.ac.kr.
Euiheon ChungDepartment of Biomedical Science and Engineering, Gwangju Institute of Science and Technology, Gwangju, South Korea. ogong50@gist.ac.kr.

Funding

AI-based GIST Research Scientist Project grant 2025Korean government (MSIT) RS-2023-00264409National Research Foundation of Korea RS-2025-00522868National Research Foundation of Korea RS-2025-00573499
6 · The paper itself

Abstract

Diabetic neuropathy (DN) is a prevalent and debilitating complication of diabetes, significantly impairing quality of life through chronic pain, sensory deficits, and motor dysfunction. Despite its widespread impact, current rodent behavioral assessments using 2D tracking methods primarily quantify basic locomotion, such as distance and speed, but lack resolution to detect subtle, pattern-based motor impairments characteristic of DN. This study employed MoSeq-based 3D behavioral profiling combined with unsupervised machine learning to identify subtle yet significant alterations in nicotinamide (NA)- and streptozotocin (STZ)-induced DN mouse models. Our analysis identified 22 distinct behavioral syllables, with DN mice exhibiting increased stress-associated behaviors such as head weaving, wall jumping, and nasal hesitancy, while displaying decreased locomotor activities including walking and rearing. These alterations were accompanied by heightened mechanical sensitivity indicative of neuropathic pain and a more predictable, less exploratory behavioral transition pattern, suggesting a restricted behavioral repertoire rather than improved motor coordination. Additionally, MoSeq-based profiling enabled detailed analysis of movement organization and temporal transitions, highlighting stereotyped behavioral sequences and notably decreased exploratory behaviors in DN mice. These behavioral patterns indicate that DN-associated pain is more strongly related to impairments in behavioral adaptability and higher-order motor planning than to simple reductions in movement, suggesting underlying dysfunctions in sensorimotor or cognitive control circuits. These findings indicate that MoSeq can be used as a valuable tool for high-resolution behavioral quantification in diabetic neuropathic animal pain model, enabling refined evaluation of neuropathic phenotypes and therapeutic efficacy in preclinical studies.

Indexed as

Behavior, AnimalDiabetes Mellitus, ExperimentalDiabetic NeuropathiesNeuralgiaAnimalsDisease Models, AnimalLocomotionMaleMiceMice, Inbred C57BL

Identifiers

PMID40301473
PMCPMC12041494

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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.