Amel Benamara, Nedjoud Grara, Samira Bensoltane, Laid Bouchaala, Amel Laouar, Kamila Grara, Hadia Hemmami, Boudjahem Abdelghani, Ali Abbas Aslam, Mahmood Ahmed
{"title":"螺旋苋对氧化铁纳米颗粒暴露的代谢和氧化反应:个体和联合(Fe₂O₃/SiO₂)效应","authors":"Amel Benamara, Nedjoud Grara, Samira Bensoltane, Laid Bouchaala, Amel Laouar, Kamila Grara, Hadia Hemmami, Boudjahem Abdelghani, Ali Abbas Aslam, Mahmood Ahmed","doi":"10.1007/s11051-025-06361-8","DOIUrl":null,"url":null,"abstract":"<div><p>This study evaluates the toxicity of iron oxide nanoparticles (Fe<sub>2</sub>O<sub>3</sub> NPs) alone and in combination with silica nanoparticles (SiO<sub>2</sub> NPs) on <i>Helix aspersa</i>. Snails were exposed to escalating concentrations (0, 5000, 10,000, 15,000 μg/g of flour) of Fe<sub>2</sub>O<sub>3</sub> NPs and a mixture of Fe<sub>2</sub>O<sub>3</sub> and SiO<sub>2</sub> NPs for 28 days to assess impacts on metabolic parameters, oxidative stress, and neurotoxicity. Fe<sub>2</sub>O<sub>3</sub> NPs significantly increased protein levels; the mixture exhibited a more pronounced effect, with significantly increased protein levels, particularly in the hepatopancreas and kidneys. Lipid levels generally decreased across all treatments, suggesting significant metabolic disruption. Carbohydrate responses were tissue-specific and differed significantly between single and combined exposures, highlighting complex responses to nanoparticle treatments. Malondialdehyde (MDA), a marker of lipid peroxidation, demonstrated a significant increase in all treatments compared to the control group. The mixture treatment caused divergent MDA responses, with higher levels observed in the hepatopancreas and lower levels in the kidneys than in single NP treatments. Glutathione (GSH) levels showed complex tissue-specific changes with mixture exposure, with reductions in the hepatopancreas and increases in the kidney. Furthermore, glutathione S-transferase (GST), catalase (CAT), and glutathione peroxidase (GPx) were altered, reflecting cellular stress responses. Notably, acetylcholinesterase (AChE) activity, a marker of neurotoxicity, was significantly reduced in all treated groups. These findings demonstrate that Fe<sub>2</sub>O<sub>3</sub> NPs, individually and combined with SiO<sub>2</sub> NPs, induce significant metabolic dysregulation, oxidative stress, and neurotoxicity in <i>H. aspersa</i>. This study underscores the potential ecological risks of NPs contamination and the importance of further research into long-term effects and combined exposures. Further understanding of the possible impact of NPs exposure on agricultural practices and human health is needed.</p></div>","PeriodicalId":653,"journal":{"name":"Journal of Nanoparticle Research","volume":"27 6","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2025-06-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Metabolic and oxidative responses in Helix aspersa to iron oxide nanoparticle exposure: individual and combined (Fe₂O₃/SiO₂) effects\",\"authors\":\"Amel Benamara, Nedjoud Grara, Samira Bensoltane, Laid Bouchaala, Amel Laouar, Kamila Grara, Hadia Hemmami, Boudjahem Abdelghani, Ali Abbas Aslam, Mahmood Ahmed\",\"doi\":\"10.1007/s11051-025-06361-8\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>This study evaluates the toxicity of iron oxide nanoparticles (Fe<sub>2</sub>O<sub>3</sub> NPs) alone and in combination with silica nanoparticles (SiO<sub>2</sub> NPs) on <i>Helix aspersa</i>. Snails were exposed to escalating concentrations (0, 5000, 10,000, 15,000 μg/g of flour) of Fe<sub>2</sub>O<sub>3</sub> NPs and a mixture of Fe<sub>2</sub>O<sub>3</sub> and SiO<sub>2</sub> NPs for 28 days to assess impacts on metabolic parameters, oxidative stress, and neurotoxicity. Fe<sub>2</sub>O<sub>3</sub> NPs significantly increased protein levels; the mixture exhibited a more pronounced effect, with significantly increased protein levels, particularly in the hepatopancreas and kidneys. Lipid levels generally decreased across all treatments, suggesting significant metabolic disruption. Carbohydrate responses were tissue-specific and differed significantly between single and combined exposures, highlighting complex responses to nanoparticle treatments. Malondialdehyde (MDA), a marker of lipid peroxidation, demonstrated a significant increase in all treatments compared to the control group. The mixture treatment caused divergent MDA responses, with higher levels observed in the hepatopancreas and lower levels in the kidneys than in single NP treatments. Glutathione (GSH) levels showed complex tissue-specific changes with mixture exposure, with reductions in the hepatopancreas and increases in the kidney. Furthermore, glutathione S-transferase (GST), catalase (CAT), and glutathione peroxidase (GPx) were altered, reflecting cellular stress responses. Notably, acetylcholinesterase (AChE) activity, a marker of neurotoxicity, was significantly reduced in all treated groups. These findings demonstrate that Fe<sub>2</sub>O<sub>3</sub> NPs, individually and combined with SiO<sub>2</sub> NPs, induce significant metabolic dysregulation, oxidative stress, and neurotoxicity in <i>H. aspersa</i>. This study underscores the potential ecological risks of NPs contamination and the importance of further research into long-term effects and combined exposures. 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Metabolic and oxidative responses in Helix aspersa to iron oxide nanoparticle exposure: individual and combined (Fe₂O₃/SiO₂) effects
This study evaluates the toxicity of iron oxide nanoparticles (Fe2O3 NPs) alone and in combination with silica nanoparticles (SiO2 NPs) on Helix aspersa. Snails were exposed to escalating concentrations (0, 5000, 10,000, 15,000 μg/g of flour) of Fe2O3 NPs and a mixture of Fe2O3 and SiO2 NPs for 28 days to assess impacts on metabolic parameters, oxidative stress, and neurotoxicity. Fe2O3 NPs significantly increased protein levels; the mixture exhibited a more pronounced effect, with significantly increased protein levels, particularly in the hepatopancreas and kidneys. Lipid levels generally decreased across all treatments, suggesting significant metabolic disruption. Carbohydrate responses were tissue-specific and differed significantly between single and combined exposures, highlighting complex responses to nanoparticle treatments. Malondialdehyde (MDA), a marker of lipid peroxidation, demonstrated a significant increase in all treatments compared to the control group. The mixture treatment caused divergent MDA responses, with higher levels observed in the hepatopancreas and lower levels in the kidneys than in single NP treatments. Glutathione (GSH) levels showed complex tissue-specific changes with mixture exposure, with reductions in the hepatopancreas and increases in the kidney. Furthermore, glutathione S-transferase (GST), catalase (CAT), and glutathione peroxidase (GPx) were altered, reflecting cellular stress responses. Notably, acetylcholinesterase (AChE) activity, a marker of neurotoxicity, was significantly reduced in all treated groups. These findings demonstrate that Fe2O3 NPs, individually and combined with SiO2 NPs, induce significant metabolic dysregulation, oxidative stress, and neurotoxicity in H. aspersa. This study underscores the potential ecological risks of NPs contamination and the importance of further research into long-term effects and combined exposures. Further understanding of the possible impact of NPs exposure on agricultural practices and human health is needed.
期刊介绍:
The objective of the Journal of Nanoparticle Research is to disseminate knowledge of the physical, chemical and biological phenomena and processes in structures that have at least one lengthscale ranging from molecular to approximately 100 nm (or submicron in some situations), and exhibit improved and novel properties that are a direct result of their small size.
Nanoparticle research is a key component of nanoscience, nanoengineering and nanotechnology.
The focus of the Journal is on the specific concepts, properties, phenomena, and processes related to particles, tubes, layers, macromolecules, clusters and other finite structures of the nanoscale size range. Synthesis, assembly, transport, reactivity, and stability of such structures are considered. Development of in-situ and ex-situ instrumentation for characterization of nanoparticles and their interfaces should be based on new principles for probing properties and phenomena not well understood at the nanometer scale. Modeling and simulation may include atom-based quantum mechanics; molecular dynamics; single-particle, multi-body and continuum based models; fractals; other methods suitable for modeling particle synthesis, assembling and interaction processes. Realization and application of systems, structures and devices with novel functions obtained via precursor nanoparticles is emphasized. Approaches may include gas-, liquid-, solid-, and vacuum-based processes, size reduction, chemical- and bio-self assembly. Contributions include utilization of nanoparticle systems for enhancing a phenomenon or process and particle assembling into hierarchical structures, as well as formulation and the administration of drugs. Synergistic approaches originating from different disciplines and technologies, and interaction between the research providers and users in this field, are encouraged.