# Characteristics of Scar Formation After Intracerebral Hemorrhage in Aged Rats: Effects of Deferoxamine

**Authors:** Xiongjie Fu, Yingfeng Wan, Ya Hua, Guohua Xi, Richard F. Keep

PMC · DOI: 10.3390/cells14151127 · Cells · 2025-07-22

## TL;DR

This study explores how brain scars form after a type of stroke in old rats and shows that a drug called deferoxamine may help reduce damage and improve recovery.

## Contribution

The study reveals new insights into glial scar formation after ICH in aged rats and identifies deferoxamine as a potential therapeutic agent.

## Key findings

- Deferoxamine reduced iron accumulation and astrogliosis while increasing oligodendrocyte presence in aged rats after ICH.
- Glial scar composition shifted from microglia to astrocytes over time, with iron-related markers concentrated in the scar core.
- By day 60, persistent neuronal loss was observed in DARPP-32-negative regions following ICH.

## Abstract

Intracerebral hemorrhage (ICH), a severe stroke subtype common in the elderly, often results in high morbidity and mortality, with limited treatment options for long-term recovery. While glial scar formation is increasingly recognized as key to central nervous system (CNS) repair, its role and characteristics in the aging brain post-ICH remain unclear. This study investigated glial scar formation after ICH (100 μL autologous blood injected into the right basal ganglia model) in aged Fischer 344 rats and assessed the effects of deferoxamine (DFX) treatment. Histological and immunohistochemical analyses were conducted on days 7, 28, and 60 post-ICH using cell-specific and iron-related markers, with DFX administered at 100 mg/kg daily for 14 days in separate groups. Over time, the lesion core showed increased hemosiderin accumulation and astrogliosis. By day 60, the area of astrogliosis corresponded to an area with persistent neuronal loss (DARPP-32-negative). Glial composition shifted from microglia dominance on day 28 to astrocyte predominance by day 60. DFX treatment reduced iron deposition, astrogliosis, and DARPP-32-negative regions while enhancing oligodendrocyte presence. Iron-related markers (HO-1, ferritin, Perls’ staining) and PDGFRβ-positive fibrotic cells were concentrated in the scar core. These findings provide novel insights into scar formation after ICH in aged rats and suggest DFX as a potential therapy to improve outcomes in elderly stroke patients.

## Linked entities

- **Proteins:** PPP1R1B (protein phosphatase 1 regulatory inhibitor subunit 1B), HMOX1 (heme oxygenase 1), ferritin (soma ferritin-like), PDGFRB (platelet derived growth factor receptor beta)
- **Diseases:** intracerebral hemorrhage (MONDO:0013792), stroke (MONDO:0005098)

## Full-text entities

- **Genes:** Ppp1r1b (protein phosphatase 1, regulatory (inhibitor) subunit 1B) [NCBI Gene 360616] {aka Darpp-32, Darpp32}, Hmox1 (heme oxygenase 1) [NCBI Gene 24451] {aka HEOXG, Heox, Hmox, Ho-1, Ho1, hsp32}, Pdgfrb (platelet derived growth factor receptor beta) [NCBI Gene 24629] {aka PDGFR-1}
- **Diseases:** ICH (MESH:D002543), stroke (MESH:D020521), astrogliosis (MESH:D005911), neuronal loss (MESH:D009410)
- **Chemicals:** DFX (MESH:D003676), Iron (MESH:D007501)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12346331/full.md

## References

47 references — full list in the complete paper: https://tomesphere.com/paper/PMC12346331/full.md

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Source: https://tomesphere.com/paper/PMC12346331