# Unbiased quantification of persistent postural and motor deficits following spinal cord injury in mice

**Authors:** Sarah S. Jobbins, Vihaan Pande, Chih-Wei Zeng, Helen Poldsam, Allan-Hermann Pool, Chun-Li Zhang, Helen C. Lai

PMC · DOI: 10.1371/journal.pone.0343998 · 2026-03-06

## TL;DR

This study uses advanced tracking and machine learning to identify long-lasting postural and motor impairments in mice after spinal cord injury, which traditional methods miss.

## Contribution

The study introduces an unbiased, quantitative method using high-speed video and machine learning to assess persistent motor and postural deficits after SCI.

## Key findings

- SCI causes long-term postural changes like reduced hindpaw spacing and altered hindpaw angles beyond 42 days post-injury.
- Motor deficits include reduced locomotor activity, decreased exploration, and disrupted fore-to-hindpaw speed ratios.
- Behavioral motif analysis reveals altered motor patterns after SCI, while sensory deficits return to baseline by 21 days.

## Abstract

Spinal cord injury (SCI) causes multifaceted postural and motor impairments that are challenging to quantify. Conventional behavioral tests, such as the Basso mouse scale (BMS), rely on qualitative observations, which do not detect subtle yet significant functional deficits. To perform unbiased and quantitative evaluation of motor function and posture after SCI, we employed high-speed video tracking with machine learning-based whole body pose estimation and weight-bearing analyses using the Blackbox system in freely moving mice. We found enduring alterations in posture induced by SCI not captured by conventional metrics. Postural deficits included reduced hindpaw spacing with concomitant increased forepaw spacing, narrowed femur width, and altered hindpaw angles, which remained evident beyond 42 days post-injury (dpi). Furthermore, sustained deficits in locomotor activity were identified as decreased distance traveled, decreased exploratory behavior, and disrupted fore-to-hindpaw speed ratio. Additionally, we analyzed behavioral motifs using Keypoint MoSeq software and found frequency changes in unique motor syllables correlating with forward acceleration and turning after SCI. Interestingly, while motor deficits persisted, sensory deficits, such as thermal and mechanical sensitivity, returned to baseline levels by 21 days after injury in C57BL/6J mice, with no subsequent hypersensitivity. Lastly, we developed a web-based application to assist in visualization and analyses of Blackbox-based kinematic data. Altogether, our study identifies distinct postural and motor deficits pre- and post-SCI using accurate, unbiased, and quantitative behavioral assessments. By tracking the unique features of motor recovery trajectories, researchers can more accurately assess the effectiveness of SCI therapeutic strategies.

## Linked entities

- **Diseases:** spinal cord injury (MONDO:0043797)

## Full-text entities

- **Genes:** Pdgfrb (platelet derived growth factor receptor, beta polypeptide) [NCBI Gene 18596] {aka CD140b, PDGFR-1, Pdgfr}, Gfap (glial fibrillary acidic protein) [NCBI Gene 14580]
- **Diseases:** hypersensitivity (MESH:D004342), neuropathic pain (MESH:D009437), contusion (MESH:D003288), motor (MESH:D000068079), tissue damage (MESH:D017695), allodynia (MESH:D006930), mortality (MESH:D003643), injury lesion (MESH:D001927), Postural (MESH:D054972), loss of sensation (MESH:D006987), scar (MESH:D002921), deficits in gait (MESH:D020233), sensory (MESH:D009477), SCI (MESH:D013119), hindlimb deficits (MESH:D009461), pain (MESH:D010146), urinary obstruction (MESH:D001748), inflammation (MESH:D007249), anxiety (MESH:D001007), sensory deficits (MESH:D012678), impairments (MESH:D060825), deficits in locomotor (MESH:D001523)
- **Chemicals:** PFA (MESH:C003043), sucrose (MESH:D013395), CO2 (MESH:D002245), calcium (MESH:D002118), DAPI (MESH:C007293), PBS (-), Alexa Fluor 488 (MESH:C000711379), Alexa Fluor 555 (MESH:C000608607), xylazine (MESH:D014991)
- **Species:** Gallus gallus (bantam, species) [taxon 9031], Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** /6N — Mus musculus (Mouse), Transformed cell line (CVCL_D461), C57BL/6J — Mus musculus (Mouse), Transformed cell line (CVCL_C0MW), BALB/c — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0184), C57BL/6 — Mus musculus (Mouse), Transformed cell line (CVCL_C0MU)

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12965682/full.md

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Source: https://tomesphere.com/paper/PMC12965682