# Neural progenitor cell transplantation results in structural and functional recovery in a rat model of cerebral palsy

**Authors:** Maryam Tavakoli Lakeh, Seyed Massood Nabavi, Fatemeh Rouhollah, Koorosh Shahpasand, Sahar Kiani

PMC · DOI: 10.22038/ijbms.2025.85616.18508 · Iranian Journal of Basic Medical Sciences · 2025-01-01

## TL;DR

This study shows that transplanting neural progenitor cells in a rat model of cerebral palsy can reduce brain damage and inflammation.

## Contribution

The novel contribution is demonstrating that NPC transplantation can reduce inflammation and brain lesions in a rat model of CP.

## Key findings

- Transplantation of NPCs reduced inflammation in the brain of CP neonates.
- The hypoxia-ischemia model in pregnant rats reliably mimics human CP pathology.
- NPCs showed potential for regulating astrogenesis and reducing brain lesions.

## Abstract

Cerebral palsy (CP) is the most prevalent pediatric neurodevelopmental disorder. Stem cell therapy is a promising way to treat brain disorders, including CP. This study sought to establish a model using pregnant rats to induce CP similarly to that observed in humans. This approach aims to enhance our understanding of the mechanisms underlying CP and explores the potential for healing brain injuries through the transplantation of neural progenitor cells (NPCs).

In this experimental study, stress conditions were induced to create a CP model in neonatal rats. Initially, the uterine vein was blocked in pregnant rats to induce hypoxic conditions. Consequently, histological analyses are performed to assess the extent of brain damage in rats.

The findings indicated that the CP group exhibited notable pathological alterations, as shown by histochemical analysis, which revealed lesions in the cortical brain tissues of neonatal rats. After confirming our CP model, NPCs were transplanted into the motor cortex of CP neonates (PND7) by microinjection. After two days, the neonates were sacrificed, and the brain tissue was pathologically analyzed. Our study shows that transplantation of neural progenitor cells decreases inflammation and regulation of astrogenesis.

The induction of hypoxia-ischemia (HI) in the uterus appears to be a reliable animal model for studying CP mechanisms. Additionally, our research demonstrates that the transplantation of NPCs is a promising therapeutic approach for treating CP. This advancement will enhance our comprehension and aid in the refinement of cellular therapeutic strategies.

## Linked entities

- **Diseases:** cerebral palsy (MONDO:0006497)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Diseases:** hypoxia (MESH:D000860), inflammation (MESH:D007249), CP (MESH:D002547), ischemia (MESH:D007511), brain injuries (MESH:D001930), hypoxic (MESH:D002534), neurodevelopmental disorder (MESH:D002658), brain damage (MESH:D001925), brain disorders (MESH:D001927), HI (MESH:D020925)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

12 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12340414/full.md

## References

49 references — full list in the complete paper: https://tomesphere.com/paper/PMC12340414/full.md

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Source: https://tomesphere.com/paper/PMC12340414