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Green-Synthesized Silver Nanoparticles with Nigella sativa: A Multifaceted Approach against Parkinson's Disease in
Salma H Hassan1, Iman A Sharaf1, Amal Suliman Mohamed1
1Department of Biochemistry, Medical Research Institute, Alexandria University, 165 El-Horreya Avenue, EL-Hadara, Alexandria 21561, Egypt.
ACS Chemical Neuroscience
|September 19, 2025
Summary
Green synthesized silver nanoparticles from Nigella sativa (NS-AgNPs) show promise for Parkinson's disease (PD) management. NS-AgNPs improved motor function, reduced toxic protein aggregation, and restored neurotransmitter levels in a PD rat model.
Area of Science:
- Neuroscience and Pharmacology
- Nanomedicine
- Biochemistry
Background:
- Parkinson's disease (PD) is a progressive neurodegenerative disorder with limited treatment options as levodopa efficacy wanes.
- Existing treatments do not halt disease progression, necessitating novel therapeutic strategies.
- Green synthesis of silver nanoparticles using Nigella sativa (NS-AgNPs) offers potential pharmacological benefits.
Purpose of the Study:
- To evaluate the therapeutic and neuroprotective effects of NS-AgNPs in a rotenone-induced Parkinson's disease rat model.
- To investigate the impact of NS-AgNPs on histological, behavioral, α-synuclein aggregation, oxidative stress, neurotransmitter levels, apoptosis, and specific microRNAs (miR-34c and miR-124).
Main Methods:
- A Parkinson's disease-like model was established in rats via daily rotenone injections for 30 days.
- Treatment groups included NS-AgNPs, Sinemet, and simultaneous rotenone and NS-AgNPs administration.
- Evaluations encompassed histological analysis, behavioral tests, α-synuclein levels, oxidative stress markers, neurotransmitter assays, apoptosis markers, and microRNA expression analysis.
Main Results:
- Rotenone-induced PD model rats exhibited disrupted striatal architecture, increased α-synuclein aggregation, oxidative stress, inflammation, apoptosis, and reduced neurotransmission and microRNA levels.
- Sinemet treatment showed moderate improvements in histology, behavior, neurotransmission, and oxidative stress.
- NS-AgNPs significantly ameliorated PD-like symptoms, modulated miR-34a and miR-124, increased dopamine, reduced α-synuclein aggregation, inhibited microglial activation and apoptosis, decreased oxidative stress, and upregulated VMAT2, with no observed adverse effects.
Conclusions:
- NS-AgNPs demonstrate significant therapeutic and neuroprotective potential against Parkinson's disease progression.
- The mechanism involves modulating key PD pathways, including microRNA expression, dopamine levels, α-synuclein aggregation, and oxidative stress.
- NS-AgNPs represent a promising, safe, and effective alternative agent for Parkinson's disease management.
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