# Evaluation of the Effects of the Anti-Inflammatory and Antioxidant Properties of Aloperine on Recovery in an Experimental Sciatic Nerve Injury Model

**Authors:** Mehmet Ertanıdır, Erkan Sabri Ertaş, Ali Güleç, Bahadır Öztürk, Nejat Ünlükal, Sadettin Çiftci

PMC · DOI: 10.3390/antiox15010126 · Antioxidants · 2026-01-19

## TL;DR

This study explores how aloperine, a natural compound, can improve recovery after sciatic nerve injury by reducing inflammation and oxidative stress in rats.

## Contribution

This is the first study to investigate aloperine's effects on peripheral nerve repair, revealing its novel therapeutic potential.

## Key findings

- Aloperine improved functional recovery and reduced inflammation in injured nerves.
- The compound decreased oxidative stress and preserved axonal structure in treated rats.
- Aloperine elevated anti-inflammatory IL-10 while lowering pro-inflammatory TNF-α.

## Abstract

Peripheral nerve injuries affect 13–23 out of 100,000 people annually, with Wallerian degeneration and subsequent inflammatory/oxidative responses critically impacting recovery. Aloperine, a natural alkaloid from Sophora alopecuroides L., exhibits potent anti-inflammatory and antioxidant properties but has never been studied for nerve repair. In this study, we aimed to investigate whether aloperine could enhance peripheral nerve regeneration by modulating inflammation and oxidative stress in a rat sciatic nerve injury model. Thirty male Wistar rats underwent sciatic nerve neurotmesis with epineural repair. Animals were divided into surgical controls (Group A), aloperine-treated rats (Group B; single 100 mg/kg intraperitoneal dose), and intact controls (Group C). After 8 weeks, outcomes were assessed via functional tests (pinprick, hot plate, extensor postural thrust), biochemical analyses (TNF-α, IL-6, IL-10, TOS/TAS), and histomorphometric evaluations (axon counts, diameter indices, immunohistochemistry). Aloperine treatment significantly improved functional recovery, with near-normal hot plate latency and motor performance. Biochemically, it reduced pro-inflammatory markers (TNF-α) while elevating IL-10. Oxidative stress was attenuated. Histologically, treated nerves showed better-preserved axonal architecture (reduced inflammation). This first investigation of aloperine for nerve repair demonstrates its therapeutic potential through dual anti-inflammatory and antioxidant mechanisms, significantly improving functional and structural outcomes. These findings support its development as a novel treatment for peripheral nerve injuries.

## Linked entities

- **Chemicals:** Aloperine (PubChem CID 162147), IL-6 (PubChem CID 165368475), IL-10 (PubChem CID 146070)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Il6 (interleukin 6) [NCBI Gene 24498] {aka ILg6, Ifnb2}, Tnf (tumor necrosis factor) [NCBI Gene 24835] {aka RATTNF, TNF-alpha, Tnfa}, Il10 (interleukin 10) [NCBI Gene 25325] {aka IL10X, If2a}
- **Diseases:** Sciatic Nerve Injury (MESH:D020426), Wallerian degeneration (MESH:D014855), Inflammatory (MESH:D007249), Peripheral nerve injuries (MESH:D059348)
- **Chemicals:** Aloperine (MESH:C062701), alkaloid (MESH:D000470)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Sophora alopecuroides (species) [taxon 200492]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12837677/full.md

## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12837677/full.md

## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC12837677/full.md

---
Source: https://tomesphere.com/paper/PMC12837677