# Therapeutic effects of Lactobacillus rhamnosus, thymol and their combination against neurotoxicity in propionic acid (PA)-induced autistic rats: insights into the role of the Nrf2/HO-1, Wnt3/β-catenin/GSK3β BDNF/p-TrkB/CREB, pI3K/Akt/mTOR, AMPK/SIRT-1, and PERK/CHOP/Bcl-2 pathways

**Authors:** Hoda A. Salem, Nermin I. Rizk, Moustafa H. AbdelSalam, Rehab Ahmed, Hebatallah Husseini Atteia, Ahmed M. E. Hamdan, Areej A. Alghamdi, Manar A. Alghusn, Renad A. Alatawi, Rawan A. Atallah, Maryam M. Alfuhaymani, Hatun A. Alqahtani, Karema Abu-Elfotuh

PMC · DOI: 10.3389/fphar.2025.1728908 · 2026-01-28

## TL;DR

This study shows that Lactobacillus rhamnosus, thymol, or both can reduce autism-like symptoms in rats by improving brain function and reducing inflammation and stress.

## Contribution

The study reveals the combined therapeutic potential of a probiotic and a phytochemical in modulating multiple molecular pathways in autism.

## Key findings

- Treatment improved memory, learning, and attention in autistic rats.
- The combination reduced oxidative stress, inflammation, and apoptosis in the brain.
- Key pathways like BDNF/p-TrkB/CREB and Nrf2/HO-1 were significantly modulated.

## Abstract

Autism spectrum disorder (ASD) is a neurodevelopmental disease characterized by repetitive behaviors and a lack of social communication. The role of probiotics, phytochemicals and their combination phytochemicals as treatment options for ASD is still under study.

This study aimed to evaluate the associated molecular pathways and explore the impact of Lactobacillus rhamnosus (L. rhamnosus), thymol (Thy) and their combination on propionic acid (PA)-induced ASD rats.

Fifty 3-week-old male albino rat pups were randomly distributed into five groups. The groups included a control group, a PA-induced ASD group, in which PA (250 mg/kg, p.o.) was administered for 3 days, and three other groups that received PA (250 mg/kg, p.o.) for 3 days along with either L. rhamnosus (1 × 10^6 CFU/day, p.o), Thy (30 mg/kg/day, p.o), or both. Brain tissues were collected for biochemical, histological, and immunohistochemical studies following behavioral evaluations.

Compared with the group administered only PA, treatment with L. rhamnosus, Thy and their combination significantly improved the neurobehavioral deficits in the autistic group. Improvements were observed in tests assessing memory consolidation, learning capacity, attention, spatial memory, locomotor activity, and contextual information processing. In addition to histopathological improvements, L. rhamnosus, Thy and their combination demonstrated notable ameliorative effects on PA-induced abnormalities in brain neurotransmitters, oxidative stress, inflammation, apoptosis, and endoplasmic reticulum (ER) stress and autophagy biomarkers. Furthermore, treatment with L. rhamnosus, Thy and their combination improved abnormalities in the tested biomarkers and modulated associated pathways, including significant upregulation of BDNF, TrkB, CREB, Nrf2, and HO-1 content and downregulation of TLR4/NF-κB-mediated neuroinflammation, leading to substantial improvements in ASD symptoms.

Our results suggest that L. rhamnosus, Thy and their combination have promising therapeutic potentials in alleviating biochemical and behavioral deficits in PA-induced autism. These effects may be mediated by halting apoptosis, inflammation, and endoplasmic reticulum stress, inducing autophagy, and improving different biomarkers and modulation pathways, such as Wnt3/β-catenin/GSK3β, pI3K/p-Akt/mTOR, and BDNF/p-TrkB/CREB.

L. rhamnosus is Lactobacillus rhamnosus.Flowchart illustrating the effects of L. rhamnosus, Thymol, or both on neurological functions. It details behavioral tests and biochemical analyses on propionic acid's effects, such as impaired neurotransmission and neurodevelopmental deficits. Key areas include apoptosis, autophagy, neuroinflammation, and oxidative stress, with specific protein markers indicated for each process.

L. rhamnosus is Lactobacillus rhamnosus.

## Linked entities

- **Genes:** GABPA (GA binding protein transcription factor subunit alpha) [NCBI Gene 2551], HMOX1 (heme oxygenase 1) [NCBI Gene 3162], WNT3 (Wnt family member 3) [NCBI Gene 7473], ctnnb1.S (catenin beta 1 S homeolog) [NCBI Gene 380441], GSK3B (glycogen synthase kinase 3 beta) [NCBI Gene 2932], BDNF (brain derived neurotrophic factor) [NCBI Gene 627], NTRK2 (neurotrophic receptor tyrosine kinase 2) [NCBI Gene 4915], CREB1 (cAMP responsive element binding protein 1) [NCBI Gene 1385], PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha) [NCBI Gene 5290], AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207], MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475], PRKAA1 (protein kinase AMP-activated catalytic subunit alpha 1) [NCBI Gene 5562], SIRT1 (sirtuin 1) [NCBI Gene 23411], EIF2AK3 (eukaryotic translation initiation factor 2 alpha kinase 3) [NCBI Gene 9451], DDIT3 (DNA damage inducible transcript 3) [NCBI Gene 1649], BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596], TLR4 (toll like receptor 4) [NCBI Gene 7099], NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790]
- **Chemicals:** propionic acid (PubChem CID 1032), thymol (PubChem CID 6989)
- **Diseases:** autism spectrum disorder (MONDO:0005258), ASD (MONDO:0006664)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Diseases:** neurobehavioral deficits (MESH:D019954), neuroinflammation (MESH:D000090862), neurotoxicity (MESH:D020258), ASD (MESH:D000067877), repetitive (MESH:D012090), neurodevelopmental disease (MESH:D004194), inflammation (MESH:D007249), autism (MESH:D001321)
- **Chemicals:** PA (MESH:C029658), Thy (MESH:D013943)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Lacticaseibacillus rhamnosus (species) [taxon 47715]

## Figures

17 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12891102/full.md

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Source: https://tomesphere.com/paper/PMC12891102