# Protocol for mouse vascular dementia model and evaluation of progressive tissue damage in subcortical white matter and adjacent cortex

**Authors:** Min Tian, Irene L. Llorente, S. Thomas Carmichael

PMC · DOI: 10.1016/j.xpro.2026.104396 · STAR Protocols · 2026-03-03

## TL;DR

This paper provides a detailed protocol for creating a mouse model of vascular dementia and analyzing tissue damage in the brain.

## Contribution

A new mouse model for vascular dementia using stereotaxic microinjection and methods to evaluate progressive tissue damage.

## Key findings

- A protocol for generating a vascular dementia mouse model via microinjection of L-NIO into subcortical white matter.
- Methods to evaluate pathological features like vessel dilation, demyelination, and glial reactivity using confocal imaging and analysis tools.
- Guidance for longitudinal tracking of disease progression and cell-type-specific changes.

## Abstract

Here, we present a protocol for generating a vascular dementia (VaD) mouse model through stereotaxic microinjection of a vasoconstrictor into the subcortical white matter (WM). We describe steps for preparing the N5-(1-iminoethyl)-L-ornithine (L-NIO) solution, surgical procedures, and immunohistochemistry. We then detail procedures for confocal imaging and image analysis using ImageJ and Imaris software to evaluate key pathological features of human VaD, including vessel dilation, demyelination, glial reactivity, neuronal damage, subcortical WM atrophy, and ventriculomegaly.

For complete details on the use and execution of this protocol, please refer to Tian et al.1

•Procedures for generating a VaD mouse model via stereotaxic microinjection•Steps for quantifying core pathological features including cell-type-specific changes•Instructions for longitudinally tracking pathological progression of disease stages•Guidance on comprehensive analysis including immunohistochemistry and image processing

Procedures for generating a VaD mouse model via stereotaxic microinjection

Steps for quantifying core pathological features including cell-type-specific changes

Instructions for longitudinally tracking pathological progression of disease stages

Guidance on comprehensive analysis including immunohistochemistry and image processing

Publisher’s note: Undertaking any experimental protocol requires adherence to local institutional guidelines for laboratory safety and ethics.

Here, we present a protocol for generating a vascular dementia (VaD) mouse model through stereotaxic microinjection of a vasoconstrictor into the subcortical white matter (WM). We describe steps for preparing the N5-(1-iminoethyl)-L-ornithine (L-NIO) solution, surgical procedures, and immunohistochemistry. We then detail procedures for confocal imaging and image analysis using ImageJ and Imaris software to evaluate key pathological features of human VaD, including vessel dilation, demyelination, glial reactivity, neuronal damage, subcortical WM atrophy, and ventriculomegaly.

## Linked entities

- **Chemicals:** N5-(1-iminoethyl)-L-ornithine (PubChem CID 107984), L-NIO (PubChem CID 107984)
- **Diseases:** vascular dementia (MONDO:0004648), VaD (MONDO:1040011)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Bcl11b (B cell leukemia/lymphoma 11B) [NCBI Gene 58208] {aka 9130430L19Rik, B630002E05Rik, BCL-11B, Ctip2, Rit1}, Gfap (glial fibrillary acidic protein) [NCBI Gene 14580], Cspg4 (chondroitin sulfate proteoglycan 4) [NCBI Gene 121021] {aka 4732461B14Rik, AN2, Cspg4a, NG2}, Pdgfrb (platelet derived growth factor receptor, beta polypeptide) [NCBI Gene 18596] {aka CD140b, PDGFR-1, Pdgfr}, Cux1 (cut-like homeobox 1) [NCBI Gene 13047] {aka CDP, Cutl1, Cux, Cux-1}, Pecam1 (platelet/endothelial cell adhesion molecule 1) [NCBI Gene 18613] {aka Cd31, PECAM-1, Pecam}, Rbfox3 (RNA binding protein, fox-1 homolog (C. elegans) 3) [NCBI Gene 52897] {aka Fox-3, Hrnbp3, NeuN, Neuna60}, Nefm (neurofilament, medium polypeptide) [NCBI Gene 18040] {aka NF-M, NF160, NF165, Nef3, Nfm}, Anpep (alanyl aminopeptidase, membrane) [NCBI Gene 16790] {aka AP-M, AP-N, Apn, Cd13, P150}, Satb2 (special AT-rich sequence binding protein 2) [NCBI Gene 212712] {aka BAP002, mKIAA1034}, Iba1 (induction of brown adipocytes 1) [NCBI Gene 114737], Mbp (myelin basic protein) [NCBI Gene 17196] {aka Hmbpr, golli-mbp, jve, mld, shi}, Olig2 (oligodendrocyte transcription factor 2) [NCBI Gene 50913] {aka Bhlhb1, Olg-2, Oligo2, RK17, bHLHe19}
- **Diseases:** Infections (MESH:D007239), dilation (MESH:D002311), ischemic damage (MESH:D017202), ischemic stroke (MESH:D002544), demyelination (MESH:D003711), VaD (MESH:D015140), hypertensive (MESH:D006973), capillary occlusion (MESH:D001157), VCID (MESH:D003072), axon damage (MESH:D001480), tissue damage (MESH:D017695), memory and motor deficits (MESH:D008569), ventriculomegaly (MESH:D006849), dementia (MESH:D003704), neuronal damage (MESH:D009410), inflammatory drugs (MESH:D000081015), dryness (MESH:D014987), infarct lesion (MESH:D007238), edema (MESH:D004487), atrophy (MESH:D001284), eyes (MESH:D005134), Brain atrophy (MESH:C566985), AD (MESH:D000544), Ischemic (MESH:D002545), inflammation (MESH:D007249), bilateral or asymmetrical carotid artery stenosis (MESH:D016893), damage (MESH:D020263), axon (MESH:D012183), motor deficits (MESH:D009461), ischemia (MESH:D007511), small vessel arteriopathy (MESH:D059345), stroke (MESH:D020521), WM (MESH:D056784), neurological diseases (MESH:D020271)
- **Chemicals:** TMS (MESH:D013932), oil (MESH:D009821), glycerol (MESH:D005990), Carbide (-), aluminum (MESH:D000535), Sulfamethoxazole (MESH:D013420), L-NIO (MESH:C065027), DAPI (MESH:C007293), PBS (MESH:D007854), Iodine (MESH:D007455), citrate (MESH:D019343), Triton X (MESH:D017830), mineral oil (MESH:D008899), EDTA (MESH:D004492), oxygen (MESH:D010100), OCT (MESH:C051883), saline (MESH:D012965), ethanol (MESH:D000431), Isoflurane (MESH:D007530), water (MESH:D014867), styrene (MESH:D020058)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116], Mus musculus (house mouse, species) [taxon 10090]
- **Mutations:** C-25 C
- **Cell lines:** C57BL/6 — Mus musculus (Mouse), Transformed cell line (CVCL_C0MU)

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12969622/full.md

## References

15 references — full list in the complete paper: https://tomesphere.com/paper/PMC12969622/full.md

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Source: https://tomesphere.com/paper/PMC12969622