# Alpha-Lipoic Acid in Early-Stage Alcohol-Related Brain Damage in Rats: A Comparative Pilot Study

**Authors:** Hristian Staykov, Stela Dragomanova, Yordan Hodzhev, Valya Grigorova, Borislav Minchev, Diamara Uzunova, Ani Georgieva, Inna Sulikovska, Katerina Todorova, Elina Tsvetanova, Almira Georgieva, Miroslava Stefanova, Pendar Valadbeigi, Reni Kalfin, Rumen Nikolov, Lyubka Tancheva

PMC · DOI: 10.3390/molecules30194007 · 2025-10-07

## TL;DR

This study explores whether alpha-lipoic acid can help treat early brain damage caused by alcohol in rats, comparing it to two other drugs.

## Contribution

This is the first study to compare alpha-lipoic acid with rivastigmine and memantine in treating early-stage alcohol-related brain damage in rats.

## Key findings

- Alpha-lipoic acid improved memory and reduced Purkinje cell damage in alcohol-treated rats.
- Alpha-lipoic acid decreased lipid peroxidation by 44%, more effectively than the other drugs.
- Alpha-lipoic acid also reduced superoxide dismutase activity by 33%, similar to the reference drugs.

## Abstract

Alcohol misuse can lead to alcohol-related brain damage (ARBD), a condition linked to long-term cognitive impairment and considerable disease burden. The pharmacological characteristics of alpha-lipoic acid (ALA) make it a promising candidate for the treatment of ARBD. In this study, adult male Wistar rats were divided into eight experimental groups. Four groups received a 20% (v/v) ethanol–tap water solution ad libitum for 15 weeks to induce early-stage ARBD, while the remaining received only tap water. After 14 weeks, all groups were administered daily injections for one week with either ALA, rivastigmine, or memantine. Behavioral testing included the step-through passive avoidance and rotarod performance tests. Whole-brain biochemical analyses assessed acetylcholinesterase activity, brain-derived neurotrophic factor, and oxidative stress biomarkers. Brain weight, relative brain weight, and brain histopathological changes were also evaluated. Results showed that, similar to memantine and rivastigmine, ALA improved STL at both 24 h and 8 days and reduced ethanol-induced Purkinje cell damage. It also decreased lipid peroxidation levels by 44%, unlike the reference drugs, and superoxide dismutase activity by 33%, similar to them. No other significant changes were detected. Albeit several limitations, this is the first study comparing ALA with rivastigmine and memantine in this experimental context.

## Linked entities

- **Chemicals:** alpha-lipoic acid (PubChem CID 864), ethanol (PubChem CID 702), rivastigmine (PubChem CID 5077), memantine (PubChem CID 4054)

## Full-text entities

- **Genes:** Ache (acetylcholinesterase) [NCBI Gene 83817], Bdnf (brain-derived neurotrophic factor) [NCBI Gene 24225]
- **Diseases:** ARBD (MESH:D019973), Purkinje cell damage (MESH:D002280), cognitive impairment (MESH:D003072), Alcohol misuse (MESH:D000437)
- **Chemicals:** lipid (MESH:D008055), ALA (MESH:D008063), water (MESH:D014867), rivastigmine (MESH:D000068836), memantine (MESH:D008559), ethanol (MESH:D000431)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Figures

12 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12526403/full.md

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Source: https://tomesphere.com/paper/PMC12526403