journal article·2026-05-18Open access

Effects of iron and silver nanoparticles on Ctenopharyngodon idella’s swimming performance, their bioaccumulation, histological changes, and oxidative stress

Mian Adnan Kakakhel, Nishita Narwal, Heba Mahboub, Feras Darwish Elhajji, Salman Khan, Shi Xiaotao, Mutwakel Dabiellil, Muhammad Sarfaraz Iqbal, Esmael M. Alyami, Omar A. Almohammed

Discover Nano· Volume 21· Issue 1

Abstract

Nanoparticles (NPs) are small-sized particles that have various applications; however, these metallic particles are found to be toxic against aquatic organisms. Therefore, the current study observed the toxicity of silver nanoparticles (AgNPs) and iron oxide nanoparticles (IONPs) using Ctenopharyngodon idella by swimming behavior, bioaccumulation, histopathological alterations, and oxidative stress. Fish were exposed to AgNPs and IONPs (5.16 mg/L) for 10 days to assess their possible effects on behavioral and physiological changes. Results showed that both NPs significantly decreased the critical swimming speed (Ucrit), and found a significant correlation between body size and swimming speed. The NPs were significantly accumulated in the intestine, followed by muscles, gills, liver, and brain (p < 0.05), which resulted in histological alterations, i.e., necrosis in gill lamella and grey matter disruption in brain. In addition, the NPs resulted in oxidative stress, i.e., the superoxide dismutase enzyme in the gill was significantly increased (291.66 ± 4.04) in the IONPs group. The possible mechanisms include NP-induced gill damage and altered gill morphology, which may impair respiratory efficiency, ROS, and osmoregulation, leading to reduced swimming performance.
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Research context

OpenAlex topics: Nanoparticles: synthesis and applications · Environmental Toxicology and Ecotoxicology · Aquaculture disease management and microbiota

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (71)

Show source-provided references
1. Iwuji C, et al. Synthesis and characterization of silver nanoparticles and their promising antimicrobial effects. Chem Phys Impact. 2024;9:100758.10.1016/j.chphi.2024.100758 ↗
2. Khan Y, et al. Classification, synthetic, and characterization approaches to nanoparticles, and their applications in various fields of nanotechnology: a review. Catalysts. 2022;12:1386.10.3390/catal12111386 ↗
3. Dhand C, et al. Methods and strategies for the synthesis of diverse nanoparticles and their applications: a comprehensive overview. RSC Adv. 2015;5:105003–37.10.1039/C5RA19388E ↗
4. Abou El-Nour KMM, Eftaiha A, Al-Warthan A, Ammar RAA. Synthesis and applications of silver nanoparticles. Arab J Chem. 2010;3:135–40.10.1016/j.arabjc.2010.04.008 ↗
5. Ibrahim RE, et al. Palliative role of colloidal silver nanoparticles synthetized by moringa against Saprolegnia spp. infection in Nile tilapia: biochemical, immuno-antioxidant response, gene expression, and histopathological investigation. Aquac Rep. 2022;26:101318.10.1016/j.aqrep.2022.101318 ↗
6. Kakakhel MA, et al. Bio‐reductive synthesis of silver nanoparticles, its antibacterial efficiency, and possible toxicity in common carp fish (Cyprinus carpio). Microsc Res Tech 2023.10.1002/jemt.24427 ↗
7. Kurczewska J, Dobosz B. Recent progress and challenges regarding magnetite-based nanoparticles for targeted drug delivery. Appl Sci. 2024;14:1132.10.3390/app14031132 ↗
8. Montiel Schneider MG, et al. Biomedical applications of iron oxide nanoparticles: current insights progress and perspectives. Pharmaceutics. 2022;14:204.10.3390/pharmaceutics14010204 ↗
9. Samrot AV, Sahithya CS, Selvarani J, Purayil SK, Ponnaiah P. A review on synthesis, characterization and potential biological applications of superparamagnetic iron oxide nanoparticles. Curr Res Green Sustain Chem. 2021;4:100042.10.1016/j.crgsc.2020.100042 ↗
10. Narwal N, et al. Emerging micropollutants in aquatic ecosystems and nanotechnology-based removal alternatives: a review. Chemosphere. 2023;341:139945.10.1016/j.chemosphere.2023.139945 ↗
11. Bundschuh M, et al. Nanoparticles in the environment: Where do we come from, where do we go to? Environ Sci Eur. 2018;30:6.10.1186/s12302-018-0132-6 ↗
12. Limpiteeprakan P, Babel S, Lohwacharin J, Takizawa S. Release of silver nanoparticles from fabrics during the course of sequential washing. Environ Sci Pollut Res. 2016;23:22810–8.10.1007/s11356-016-7486-3 ↗
13. Priyadharshini SD, et al. Graphene oxide-based nanomaterials for the treatment of pollutants in the aquatic environment: Recent trends and perspectives—a review. Environ Pollut. 2022;306:119377.10.1016/j.envpol.2022.119377 ↗
14. Labille J, et al. Assessing sunscreen lifecycle to minimize environmental risk posed by nanoparticulate UV-filters–a review for safer-by-design products. Front Environ Sci. 2020;8:101.10.3389/fenvs.2020.00101 ↗
15. Ehalt Macedo H, et al. Global distribution of wastewater treatment plants and their released effluents into rivers and streams. Earth Syst Sci Data Discuss 2021;1–33.10.5194/essd-2021-214 ↗
16. Deepa G, Jeyaraj M, Magudeswaran PN. Removal of heavy metals from Chithrapuzha River water by iron oxide nanoparticles prepared via green synthesis methods. Orient J Chem. 2020. https://doi.org/10.13005/ojc/360620.10.13005/ojc/360620 ↗
17. Gutiérrez GG, et al. First evidence of anthropogenic TiO2 nanoparticles occurrence in Chilean rivers. Environ Adv. 2024;16:100536.10.1016/j.envadv.2024.100536 ↗
18. Kuznetsova OV, Keppler BK, Timerbaev AR. Analysis of engineered nanoparticles in seawater using ICP-MS-based technology: from negative to positive samples. Molecules. 2023. https://doi.org/10.3390/molecules28030994.10.3390/molecules28030994 ↗
19. Wimmer A, Markus AA, Schuster M. Silver nanoparticle levels in river water: real environmental measurements and modeling approaches—A comparative study. Environ Sci Technol Lett. 2019;6:353–8.10.1021/acs.estlett.9b00211 ↗
20. Li G, et al. Detection, distribution and environmental risk of metal-based nanoparticles in a coastal bay. Water Res. 2023;242:120242.10.1016/j.watres.2023.120242 ↗
21. Tao W, et al. Influence of silver nanoparticles on heavy metals of pore water in contaminated river sediments. Chemosphere. 2016;162:117–24.10.1016/j.chemosphere.2016.07.043 ↗
22. Zaheer Ud Din S, Shah K, Bibi N, Mahboub HH, Kakakhel MA. Recent insights into the silver nanomaterials: an overview of their transformation in the food webs and toxicity in the aquatic ecosystem. Water Air Soil Pollut. 2023;234:114.10.1007/s11270-023-06134-w ↗
23. Mattsson K, et al. Altered behavior, physiology, and metabolism in fish exposed to polystyrene nanoparticles. Environ Sci Technol. 2015;49:553–61.10.1021/es5053655 ↗
24. Khosravi-Katuli K, et al. Effects of nanoparticles in species of aquaculture interest. Environ Sci Pollut Res. 2017;24:17326–46.10.1007/s11356-017-9360-3 ↗
25. Khan SK, et al. Silver nanoparticle toxicity in rainbow trout: insights into physiological and molecular responses. Toxicol Mech Methods 2024;1–16.
26. Kumar M, et al. Toxicity ameliorative effect of vitamin E against super-paramagnetic iron oxide nanoparticles on haemato-immunological responses, antioxidant capacity, oxidative stress, and metabolic enzymes activity during exposure and recovery in Labeo rohita fingerlin. Aquac Int. 2022;30:1711–39.10.1007/s10499-022-00870-2 ↗
27. Mahboub HH, et al. Impact of silver nanoparticles exposure on neuro-behavior, hematology, and oxidative stress biomarkers of African catfish (Clarias gariepinus). Aquaculture. 2021;544:737082.10.1016/j.aquaculture.2021.737082 ↗
28. Zhao Y, Zhang L, Wang C, Xie C. Biology and ecology of grass carp in China: a review and synthesis. North Am J Fish Manag. 2020;40:1379–99.10.1002/nafm.10512 ↗
29. Kakakhel MA, et al. Long-term exposure to high-concentration silver nanoparticles induced toxicity, fatality, bioaccumulation, and histological alteration in fish (Cyprinus carpio). Environ Sci Eur. 2021;33:14.10.1186/s12302-021-00453-7 ↗
30. Kakakhel MA, et al. Hydraulic engineering affects freshwater fish swimming performance by shifting intestinal bacterial composition. A microbiological mechanism. Freshw Biol. 2025;70:e70122.10.1111/fwb.70122 ↗
31. Mu X, Cao P, Gong L, Baiyin B, Li X. A classification method for fish swimming behaviors under incremental water velocity for fishway hydraulic design. Water. 2019. https://doi.org/10.3390/w11102131.10.3390/w11102131 ↗
32. Kakakhel MA, et al. The swimming performance and transcriptomic insights into diverse gene regulation in grass carp brain under water velocity stress. Water Resour Res 2025;61:e2024WR037990.10.1029/2024WR037990 ↗
33. Guo H, et al. Effects of exercise training on the external morphology, growth performance, swimming ability, body composition and metabolism of juvenile black seabream Acanthopagrus schlegelii. Aquaculture. 2024;587:740878.10.1016/j.aquaculture.2024.740878 ↗
34. Brett JR. The respiratory metabolism and swimming performance of young sockeye salmon. J Fish Res Board Can. 1964;21:1183–226.10.1139/f64-103 ↗
35. Correia AT, Rebelo D, Marques J, Nunes B. Effects of the chronic exposure to cerium dioxide nanoparticles in Oncorhynchus mykiss: assessment of oxidative stress, neurotoxicity and histological alterations. Environ Toxicol Pharmacol. 2019;68:27–36.10.1016/j.etap.2019.02.012 ↗
36. Kakakhel MA, et al. Biological synthesis of silver nanoparticles using animal blood, their preventive efficiency of bacterial species, and ecotoxicity in common carp fish. Microsc Res Tech 2021.10.1002/jemt.23733 ↗
37. Downie AT, Illing B, Faria AM, Rummer JL. Swimming performance of marine fish larvae: review of a universal trait under ecological and environmental pressure. Rev Fish Biol Fish. 2020;30:93–108.10.1007/s11160-019-09592-w ↗
38. Chen X, et al. Optimizing fishway entrance attraction flow based on Schizothorax prenanti swimming behavior and entrance efficiency. Ethol Ecol Evol. 2025;37:510–32.10.1080/03949370.2025.2511617 ↗
39. Calfee RD, Puglis HJ, Little EE, Brumbaugh WG, Mebane CA. Quantifying fish swimming behavior in response to acute exposure of aqueous copper using computer assisted video and digital image analysis. J Vis Exp JoVE 2016;53477.10.3791/53477-v ↗
40. da Costa Araujo AP, Malafaia G. Can short exposure to polyethylene microplastics change tadpoles’ behavior? A study conducted with neotropical tadpole species belonging to order anura (Physalaemus cuvieri). J Hazard Mater. 2020;391:122214.10.1016/j.jhazmat.2020.122214 ↗
41. Farrell AP. Comparisons of swimming performance in rainbow trout using constant acceleration and critical swimming speed tests. J Fish Biol. 2008;72:693–710.10.1111/j.1095-8649.2007.01759.x ↗
42. Makaras T, Jakubowska-Lehrmann M, Jurgelėnė Ž, Šemčuk S. Exploring the effects of graphene-based nanoparticles on early salmonids cardiorespiratory responses, swimming and nesting behavior. J Xenobiotics. 2024;14:484–96.10.3390/jox14020029 ↗
43. Egbuna C, et al. Toxicity of nanoparticles in biomedical application: nanotoxicology. J Toxicol. 2021;2021:9954443.10.1155/2021/9954443 ↗
44. Laubach C, DeVries DR, Wright RA, Smith DL. The effect of temperature and acute hypoxia/hyperoxia exposure on swimming performance and kinematics of Freshwater Drum. Trans Am Fish Soc. 2023;152:460–74.10.1002/tafs.10414 ↗
45. de Oliveira Eiras MI, da Costa LS, Barbieri E. Copper II oxide nanoparticles (CuONPs) alter metabolic markers and swimming activity in zebra-fish (Danio rerio). Comp Biochem Physiol Part C Toxicol Pharmacol 2022;257:109343.10.1016/j.cbpc.2022.109343 ↗
46. Guerrera MC, et al. Micro and nano plastics distribution in fish as model organisms: histopathology, blood response and bioaccumulation in different organs. Appl Sci Basel. 2021;11:5768.10.3390/app11135768 ↗
47. Zhang K, et al. Water quality impact on fish behavior: a review from an aquaculture perspective. Rev Aquac 2024.10.1111/raq.12985 ↗
48. Thoma A, Lightfoot AP. NF-kB and inflammatory cytokine signalling: role in skeletal muscle atrophy. Muscle Atrophy 2018;267–279.10.1007/978-981-13-1435-3_12 ↗
49. Kakakhel MA, et al. Influence of biosynthesized nanoparticles exposure on mortality, residual deposition, and intestinal bacterial dysbiosis in Cyprinus carpio. Comp Biochem Physiol Part C Toxicol Pharmacol 2023;263:109473.10.1016/j.cbpc.2022.109473 ↗
50. Hajiyeva A, et al. Ultrastructural investigation of iron oxide nanoparticles accumulation in the liver of common carp (Cyprinus carpio Linnaeus, 1758). Aquat Toxicol. 2024;272:106961.10.1016/j.aquatox.2024.106961 ↗
51. Younas W, et al. Toxicity of synthesized silver nanoparticles in a widespread fish: a comparison between green and chemical. Sci Total Environ. 2022;845:157366.10.1016/j.scitotenv.2022.157366 ↗
52. Rashed MN, Gad AAE, Fathy NM. Efficiency of chemically activated raw and calcined waste fish bone for adsorption of Cd (II) and Pb (II) from polluted water. Biomass Convers Biorefinery. 2024;14:31703–20.10.1007/s13399-023-04885-4 ↗
53. Sachdev S, Ansari SA, Ansari MI, Fujita M, Hasanuzzaman M. Abiotic stress and reactive oxygen species: generation, signaling, and defense mechanisms. Antioxidants Basel. 2021;10:277.10.3390/antiox10020277 ↗
54. Redza-Dutordoir M, Averill-Bates DA. Activation of apoptosis signalling pathways by reactive oxygen species. Biochim et Biophys Acta (BBA). 2016;1863:2977–92.10.1016/j.bbamcr.2016.09.012 ↗
55. Madeira D, Narciso L, Cabral HN, Vinagre C, Diniz MS. Influence of temperature in thermal and oxidative stress responses in estuarine fish. Comp Biochem Physiol A Mol Integr Physiol. 2013;166:237–43.10.1016/j.cbpa.2013.06.008 ↗
56. Krishnasamy Sekar R. et al. Accumulation, chronicity, and induction of oxidative stress regulating genes through Allium cepa L. functionalized silver nanoparticles in freshwater common carp (Cyprinus carpio). Biol. Trace Elem. Res. 2023;201:904–925.10.1007/s12011-022-03164-z ↗
57. Batir-Marin D, et al. Exploring oxidative stress mechanisms of nanoparticles using zebrafish (Danio rerio): toxicological and pharmaceutical insights. Antioxidants. 2025;14:489.10.3390/antiox14040489 ↗
58. Strzyzewska E, Szarek J. Babinska I. Morphologic evaluation of the gills as a tool in the diagnostics of pathological conditions in fish and pollution in the aquatic environment: a review. Vet Med (Praha) 2016;61.10.17221/8763-VETMED ↗
59. Jiang W-D, et al. Impairment of gill structural integrity by manganese deficiency or excess related to induction of oxidative damage, apoptosis and dysfunction of the physical barrier as regulated by NF-κB, caspase and Nrf2 signaling in fish. Fish Shellfish Immunol. 2017;70:280–92.10.1016/j.fsi.2017.09.022 ↗
60. Xu Z, et al. Toxic effects on bioaccumulation, hematological parameters, oxidative stress, immune responses and tissue structure in fish exposed to ammonia nitrogen: a review. Animals. 2021;11:3304.10.3390/ani11113304 ↗
61. Manke A, Wang L, Rojanasakul Y. Mechanisms of nanoparticle-induced oxidative stress and toxicity, a review. BioMed Res Int. 2013;2013:1.10.1155/2013/942916 ↗
62. Mortezaee K, et al. Redox interactions and genotoxicity of metal-based nanoparticles: a comprehensive review. Chem Biol Interact. 2019;312:108814.10.1016/j.cbi.2019.108814 ↗
63. Ghazi S, Diab AM, Khalafalla MM, Mohamed RA. Synergistic effects of selenium and zinc oxide nanoparticles on growth performance, hemato-biochemical profile, immune and oxidative stress responses, and intestinal morphometry of Nile tilapia (Oreochromis niloticus). Biol Trace Elem Res. 2021. https://doi.org/10.1007/s12011-021-02631-3.10.1007/s12011-021-02631-3 ↗
64. Fadia BS, et al. Histological injury to rat brain, liver, and kidneys by gold nanoparticles is dose-dependent. ACS Omega. 2022;7:20656–65.10.1021/acsomega.2c00727 ↗
65. Kamel NA, et al. Polyethylene terephthalate nanoplastics caused hepatotoxicity in mice can be prevented by betaine: molecular and immunohistochemical insights. J Biochem Mol Toxicol. 2024;38:e70088.10.1002/jbt.70088 ↗
66. Wu D, et al. The blood–brain barrier: structure, regulation, and drug delivery. Signal Transduct Target Ther. 2023;8:217.10.1038/s41392-023-01481-w ↗
67. Chang X, Li J, Niu S, Xue Y, Tang M. Neurotoxicity of metal‐containing nanoparticles and implications in glial cells. J Appl Toxicol. 2021;41:65–81.10.1002/jat.4037 ↗
68. Chen X, et al. Research advances in the structure, function, and regulation of the gill barrier in teleost fish. Water Biol Secur. 2023;2:100139.10.1016/j.watbs.2023.100139 ↗
69. Xiang Q-Q, et al. Effect of silver nanoparticles on gill membranes of common carp: modification of fatty acid profile, lipid peroxidation and membrane fluidity. Environ Pollut. 2020;256:113504.10.1016/j.envpol.2019.113504 ↗
70. Horie M, Tabei Y. Role of oxidative stress in nanoparticles toxicity. Free Radic Res. 2021;55:331–42.10.1080/10715762.2020.1859108 ↗
71. Spaas J, et al. Oxidative stress and impaired oligodendrocyte precursor cell differentiation in neurological disorders. Cell Mol Life Sci. 2021;78:4615–37.10.1007/s00018-021-03802-0 ↗