# Natural Polyphenols Versus Standard Therapy: Effects on Neuroinflammation and Alpha-Synuclein Expression in a 1-Methyl-4-Phenyl-1,2,3,6-Tetrahydropyridine (MPTP)-Induced Mouse Model of Parkinson’s Disease

**Authors:** Shalini Singh, Karan Suneja, Ipshita Jain, Suyog Sindhu, Satyendra Singh, Rishi Pal, Rakesh Dixit, Rajendra Nath

PMC · DOI: 10.7759/cureus.103681 · Cureus · 2026-02-15

## TL;DR

This study compares natural polyphenols like resveratrol and curcumin to standard Parkinson’s treatment, finding that they may help reduce brain inflammation and alpha-synuclein buildup in mice.

## Contribution

The study provides a comparative evaluation of resveratrol, curcumin, and their combination against standard therapy in a mouse model of Parkinson’s disease.

## Key findings

- L-DOPA + carbidopa showed the greatest improvement in motor function and reduction in alpha-synuclein and TNF-alpha levels.
- Resveratrol and curcumin, especially in combination, significantly improved motor performance and reduced neuroinflammation compared to MPTP-treated mice.
- Resveratrol was more effective than curcumin as a monotherapy in mitigating PD-related changes.

## Abstract

Background

Parkinson’s disease (PD) is a progressive neurodegenerative disorder characterized by dopaminergic neuronal loss, α-synuclein aggregation, and chronic neuroinflammation. While levodopa (L-DOPA) + carbidopa remains the cornerstone of symptomatic management, long-term use is associated with motor complications, prompting interest in adjunctive therapies targeting non-dopaminergic mechanisms. Polyphenolic compounds such as resveratrol and curcumin have demonstrated neuroprotective potential through antioxidant and anti-inflammatory actions. This study aimed to comparatively evaluate the effects of L-DOPA + carbidopa, resveratrol, curcumin, and their combination, resveratrol + curcumin, on motor function and biochemical markers in a 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced mouse model of PD.

Methodology

An experimental study was conducted using 36 adult female C57BL/6 mice randomly allocated into six groups (n = 6): normal control group, MPTP group, L-DOPA + carbidopa group, resveratrol group, curcumin group, and resveratrol + curcumin group. PD was induced using intraperitoneal injection of MPTP (30 mg/kg/day for five days). Treatments were administered orally for 30 days. Motor coordination and locomotor activity were assessed using the rotarod test and open field tests at baseline (Day 0), post-MPTP induction (Day 6), and at the end of treatment (Day 37). Biochemical analysis of brain homogenates was performed to estimate α-synuclein and tumor necrosis factor-alpha (TNF-α) levels using enzyme-linked immunosorbent assay (ELISA). Statistical analysis was conducted using one-way analysis of variance (ANOVA) followed by Tukey’s post hoc test.

Results

MPTP administration resulted in significant motor impairment, elevated α-synuclein accumulation, and increased TNF-α levels compared with controls (P < 0.001). L-DOPA + carbidopa produced the greatest improvement in rotarod and open field performance and significantly reduced both α-synuclein and TNF-α levels. Resveratrol and curcumin monotherapy significantly improved motor performance and attenuated biochemical alterations compared with the MPTP group (P < 0.001 ), with resveratrol showing greater efficacy than curcumin. Combined treatment with resveratrol and curcumin resulted in superior motor recovery and greater reductions in α-synuclein and TNF-α levels than either compound alone.

Conclusions

The findings demonstrate a close association between motor dysfunction, α-synuclein accumulation, and neuroinflammation in MPTP-induced PD. L-DOPA+ carbidopa remains the most effective intervention for motor and biochemical parameters. However, resveratrol and curcumin, particularly in combination, exhibit significant neuroprotective effects and may serve as promising adjunctive strategies targeting disease-related inflammatory and synuclein-mediated pathways. These results support further investigation of polyphenolic compounds as complementary therapies in PD.

## Linked entities

- **Chemicals:** resveratrol (PubChem CID 5056), curcumin (PubChem CID 969516), levodopa (PubChem CID 6047), carbidopa (PubChem CID 34359), 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (PubChem CID 1388), TNF-alpha (PubChem CID 44356648)
- **Diseases:** Parkinson’s disease (MONDO:0005180)

## Full-text entities

- **Genes:** Snca (synuclein, alpha) [NCBI Gene 20617] {aka NACP, alpha-Syn, alphaSYN}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}
- **Diseases:** neuronal loss (MESH:D009410), motor dysfunction (MESH:D000068079), inflammatory (MESH:D007249), PD (MESH:D010300), Neuroinflammation (MESH:D000090862), neurodegenerative disorder (MESH:D019636)
- **Chemicals:** Polyphenols (MESH:D059808), L-DOPA (MESH:D007980), carbidopa (MESH:D002230), 1-Methyl-4-Phenyl-1,2,3,6-Tetrahydropyridine (MESH:D015632), curcumin (MESH:D003474), Polyphenolic compounds (-), Resveratrol (MESH:D000077185)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12996378/full.md

## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC12996378/full.md

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Source: https://tomesphere.com/paper/PMC12996378