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Cysteine-induced hormesis effect of silver nanoparticles
Zhi Guo1,2, Guiqiu Chen1,2, Guangming Zeng1,2
1College of Environmental Science and Engineering , Hunan University , Changsha 410082 , P.R. China . Email: gqchen@hnu.edu.cn ; Email: zgming@hnu.edu.cn ; ; Tel: +86 731 88822829.
Silver nanoparticles (AgNPs) exhibit a hormesis effect, increasing bacterial viability by 29.9% at low concentrations. Cysteine also induces this effect, showing a concentration-dependent response in AgNP toxicity.
Area of Science:
- Nanotechnology
- Toxicology
- Microbiology
Background:
- Silver nanoparticles (AgNPs) toxicity is well-documented.
- The hormesis effect of AgNPs, particularly at low concentrations, remains under-explored.
- Understanding hormesis is crucial for applications involving nanomaterials.
Purpose of the Study:
- To investigate the hormesis effect of silver nanoparticles (AgNPs) at low concentrations.
- To explore the role of cysteine in modulating AgNP-induced hormesis.
- To determine the concentration-dependent relationship between cysteine, AgNPs, and cellular response.
Main Methods:
- Exposure of bacterial cultures to varying concentrations of AgNPs.
- Administration of cysteine at different concentrations alongside AgNPs.
- Quantification of bacterial viability and sulfuration rates (ns/nAg).
Main Results:
- A significant hormesis effect was observed at low AgNP concentrations (0.34 mg L-1), increasing bacterial viability by 29.9%.
- Cysteine induced a hormesis effect within AgNP concentrations of 1.7–5.1 mg L-1 at a cysteine concentration of 12.5 mg L-1.
- The cysteine-induced hormesis effect demonstrated a concentration-dependent relationship, with a sulfuration rate (ns/nAg) of 6.15 showing strong cellular excitation.
Conclusions:
- Low concentrations of AgNPs can exert a beneficial hormesis effect on bacterial viability.
- Cysteine can modulate AgNP toxicity, inducing hormesis in a concentration-dependent manner.
- The sulfuration rate is a key factor in the cysteine-mediated hormesis of AgNPs, highlighting potential mechanisms for nanoparticle-cell interactions.
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