# High-resolution imaging and three-dimensional model of the feline spinal cord

**Authors:** Jonathan Harnie, Oussama Eddaoui, Khaled Ashkar, Charlène Nadeau, Stephen Mari, Sirine Yassine, Rasha Al Arab, Johannie Audet, Christian Iorio-Morin, Alain Frigon

PMC · DOI: 10.3389/fnana.2026.1764931 · Frontiers in Neuroanatomy · 2026-02-18

## TL;DR

This study provides a detailed 3D model and anatomical analysis of the feline spinal cord to improve surgical and computational approaches.

## Contribution

The creation of an open-access 3D model integrating MRI and Micro-CT data for the feline spinal cord.

## Key findings

- Significant variability in dural thickness and rootlet orientation was observed along the spinal axis.
- Dorsal root ganglia size and white/gray matter morphology varied across spinal segments.
- Cervical and lumbar levels showed prominent enlargements in spinal cord structures.

## Abstract

The spinal cord is a critical component of the central nervous system, responsible for integrating somatosensory inputs, generating motor outputs, and regulating autonomic functions. Despite its functional importance, high-resolution anatomical data spanning from high cervical to sacral levels of the spinal cord remain largely unexplored, limiting our ability to develop accurate surgical strategies, computational models, and neuromodulation protocols. Here, we performed a segment-by-segment quantitative anatomical analysis of the feline spinal cord from C3 to S2 using histology and high-resolution micro–computed tomography (Micro-CT) to evaluate key structures including the dura mater, dorsal root ganglia, rootlets, and white and gray matter. We observed significant variability in dural thickness, as well as structured changes in rootlet orientation and density along the spinal axis. Dorsal root ganglia size, along with white and gray matter morphology, varied across spinal segments, with prominent enlargements at cervical and lumbar levels. Additionally, we constructed an open-access three-dimensional model by integrating magnetic resonance imaging (MRI), Micro-CT, and high-resolution Micro-CT data into a unified spatial reference. This model enables precise spatial analysis of spinal structures and facilitates advanced computational modeling of spinal cord function and neuromodulation strategies. Our results represent a valuable resource for anatomical, surgical, and bioengineering applications aimed at improving spinal interventions.

## Full-text entities

- **Diseases:** chronic pain (MESH:D059350), spinal cord injury (MESH:D013119), trauma (MESH:D014947), dehydration (MESH:D003681), noise (MESH:D014012)
- **Chemicals:** I2 (MESH:D007455), butorphanol (MESH:D002077), sucrose (MESH:D013395), isoflurane (MESH:D007530), paraformaldehyde (MESH:C003043), KI (MESH:C066186), H2O (MESH:D014867), ethanol (MESH:D000431), eosin (MESH:D004801), LI (MESH:C010389), hematoxylin (MESH:D006416), phosphate (MESH:D010710), H&amp;E (MESH:D006371), IMS (-), paraffin (MESH:D010232), pentobarbital (MESH:D010424), Xylene (MESH:D014992), dexmedetomidine (MESH:D020927)
- **Species:** Sus scrofa (pig, species) [taxon 9823], Felis catus (cat, species) [taxon 9685], Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090], Rattus norvegicus (brown rat, species) [taxon 10116]
- **Cell lines:** C3-S2 — Canis lupus familiaris (Dog), Canine mastocytoma, Cancer cell line (CVCL_1R44), S2 — Drosophila melanogaster (Fruit fly), Spontaneously immortalized cell line (CVCL_Z232)

## Full text

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## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12956779/full.md

## References

53 references — full list in the complete paper: https://tomesphere.com/paper/PMC12956779/full.md

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Source: https://tomesphere.com/paper/PMC12956779