# Persistent Disruptions in Prefrontal Connectivity Despite Behavioral Rescue by Environmental Enrichment in a Mouse Model of Rett Syndrome

**Authors:** Sofie Ährlund‐Richter, Jonathan Harpe, Giselle Fernandes, Ruby Lam, Mriganka Sur

PMC · DOI: 10.1002/cne.70073 · The Journal of Comparative Neurology · 2025-07-17

## TL;DR

Environmental enrichment improves behavior in Rett syndrome mice but does not fix prefrontal brain connectivity issues.

## Contribution

The study shows that environmental enrichment rescues behavior but not prefrontal connectivity in Rett syndrome mice.

## Key findings

- Environmental enrichment rescued fine motor deficits and reduced anxiety in Mecp2+/− mice.
- Prefrontal cortex connectivity abnormalities persisted despite behavioral improvements from enrichment.
- BDNF levels were restored in the hippocampus but not in the prefrontal cortex with enrichment.

## Abstract

Rett syndrome, a neurodevelopmental disorder caused by loss‐of‐function mutations in the MECP2 gene, is characterized by severe motor, cognitive, and emotional impairments. Some of the deficits may result from changes in cortical connections, especially downstream projections of the prefrontal cortex (PFC), which may also be targets of restoration following rearing conditions such as environmental enrichment that alleviate specific symptoms. Here, using a heterozygous Mecp2+/−
 female mouse model closely analogous to human Rett syndrome, we investigated the impact of early environmental enrichment on behavioral deficits and PFC connectivity. Behavioral analyses revealed that enriched housing rescued fine motor deficits and reduced anxiety, with enrichment‐housed Mecp2+/−
 mice performing comparably to wild‐type (WT) controls in rotarod and open field assays. Anatomical mapping of top‐down anterior cingulate cortex (ACA) projections demonstrated altered PFC connectivity in Mecp2+/−
 mice, with increased axonal density in the somatosensory cortex and decreased density in the motor cortex compared to WT controls. ACA axons revealed shifts in hemispheric distribution, particularly in the medial network regions, with Mecp2+/−
 mice exhibiting reduced ipsilateral dominance. These changes were unaffected by enriched housing, suggesting that structural abnormalities in PFC connectivity persist despite behavioral improvements. Enriched housing rescued brain‐derived neurotrophic factor (BDNF) levels in the hippocampus but failed to restore BDNF levels in the PFC, consistent with the persistent deficits observed in prefrontal axonal projections. These findings highlight the focal nature of changes induced by reduction of MeCP2 and by exposure to environmental enrichment and suggest that environmental enrichment starting in adolescence can alleviate behavioral deficits in Mecp2+/−
 mice without reversing abnormalities in large‐scale cortical connectivity.

This study reveals that the loss of MeCP2 in Rett syndrome model mice disrupts prefrontal connectivity. Although early environmental enrichment helps mitigate behavioral deficits and restores hippocampal BDNF levels, it fails to reverse the altered prefrontal connectivity or prevent the prefrontal‐specific decline in BDNF.

## Linked entities

- **Genes:** MECP2 (methyl-CpG binding protein 2) [NCBI Gene 4204], MECP2 (methyl-CpG binding protein 2) [NCBI Gene 4204]
- **Proteins:** BDNF (brain derived neurotrophic factor)
- **Diseases:** Rett syndrome (MONDO:0010726)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Mecp2 (methyl CpG binding protein 2) [NCBI Gene 17257] {aka 1500041B07Rik, D630021H01Rik, Mbd5, WBP10}, Bdnf (brain derived neurotrophic factor) [NCBI Gene 12064]
- **Diseases:** anxiety (MESH:D001007), Rett Syndrome (MESH:D015518), motor, cognitive, and emotional impairments (MESH:D003072), neurodevelopmental disorder (MESH:D002658), motor deficits (MESH:D009461), behavioral deficits (MESH:D019958)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12269803/full.md

## References

63 references — full list in the complete paper: https://tomesphere.com/paper/PMC12269803/full.md

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Source: https://tomesphere.com/paper/PMC12269803