# Efficacy of Forward and Reverse Suturing Techniques in Enhancing Neural Regeneration and Motor Function Recovery Following Facial Nerve Axotomy

**Authors:** Jae Min Lee, Yeon Ju Oh, Sung Soo Kim, Youn-Jung Kim, Seung Geun Yeo

PMC · DOI: 10.3390/jcm15010096 · Journal of Clinical Medicine · 2025-12-23

## TL;DR

This study compares forward and reverse nerve suturing techniques in facial nerve repair, finding both improve motor recovery and reduce inflammation in rats.

## Contribution

The study reveals central facial nucleus mechanisms underlying motor recovery after facial nerve repair, regardless of graft orientation.

## Key findings

- Both forward and reverse suturing improved whisker and blink reflex scores compared to axotomy.
- Suturing increased ChAT and SIRT1 while reducing Iba-1 in the facial nucleus.
- Improved motor recovery is linked to cholinergic signaling and reduced microglial activation.

## Abstract

Background/Objectives: Facial nerve injury from conditions such as Bell’s palsy, trauma, surgery, and infection leads to facial asymmetry and motor deficits. Axotomy models reproduce peripheral nerve disruption and consequent motor impairment. To compare the effects of forward versus reverse autologous nerve suturing on neural regeneration and motor recovery within the facial nucleus after axotomy. Methods: In rats subjected to facial nerve axotomy, motor recovery was assessed at 8 weeks using whisker movement and blink reflex tests. Immunohistochemistry quantified choline acetyltransferase (ChAT), sirtuin 1 (SIRT1), and Iba-1 as indices of cholinergic function, cellular stress/inflammation modulation, and microglial activation in the facial nucleus. Results: Axotomy significantly reduced whisker and blink scores compared with sham. Both forward and reverse suturing significantly improved these behavioral outcomes versus axotomy. Within the facial nucleus, axotomy decreased ChAT- and SIRT1-positive cells and increased Iba-1 expression, while both suturing techniques increased ChAT and SIRT1 and reduced Iba-1. These changes suggest enhanced cholinergic function, mitigation of stress/inflammatory responses, and attenuation of microglial activation following repair. Conclusions: Forward and reverse suturing were each associated with improved motor function and favorable molecular and cellular changes in the facial nucleus after facial nerve axotomy. These findings support the utility of surgical repair irrespective of graft orientation and highlight involvement of key pathways—cholinergic signaling, SIRT1-related regulation, and microglial activity—in nerve restoration. This work extends our previous study, which focused on peripheral nerve regeneration after forward and reverse suturing, by elucidating how graft orientation affects central facial nucleus responses. By integrating behavioral outcomes with ChAT, Iba-1, and SIRT1 expression, the present study provides novel insight into the central mechanisms underlying motor recovery after facial nerve repair and helps explain why comparable functional outcomes are achieved regardless of graft polarity.

## Linked entities

- **Genes:** CHAT (choline O-acetyltransferase) [NCBI Gene 1103], SIRT1 (sirtuin 1) [NCBI Gene 23411], AIF1 (allograft inflammatory factor 1) [NCBI Gene 199]
- **Diseases:** Bell’s palsy (MONDO:0005665)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Chat (choline O-acetyltransferase) [NCBI Gene 290567], Aif1 (allograft inflammatory factor 1) [NCBI Gene 29427] {aka BART-1, Bart1, iba1, mrf-1}, Sirt1 (sirtuin 1) [NCBI Gene 309757] {aka Sir2}
- **Diseases:** nerve disruption (MESH:D019958), trauma (MESH:D014947), infection (MESH:D007239), inflammation (MESH:D007249), motor deficits (MESH:D009461), motor impairment (MESH:D000068079), Facial nerve injury (MESH:D020220), Bell's palsy (MESH:D020330), facial asymmetry (MESH:D005146)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12786698/full.md

## References

21 references — full list in the complete paper: https://tomesphere.com/paper/PMC12786698/full.md

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Source: https://tomesphere.com/paper/PMC12786698