{"title":"Elucidation of 28 day repeated oral dose induced genotoxicity potential of nickel (II) oxide nanoparticles in wistar albino rats","authors":"Naresh Dumala , Srilekha Chintala , Bhanuramya Mangalampalli , Rekhadevi Perumalla Venkata","doi":"10.1016/j.yrtph.2025.105858","DOIUrl":null,"url":null,"abstract":"<div><div>Nanotechnology has revolutionized industrial processing and human life by the applications of nanoparticles (NPs), especially the metal oxide ones. Nickel oxide (NiO) NPs have been used in applications including electronics and biosensors. Occupational and accidental exposure to these NPs for longer durations is apparent and the same may lead to significant health risks. In the present study, we have elucidated the genotoxic ability of NiO-NPs post repeated oral exposure for 28 days in Wistar albino rats at 50, 100, and 200 mg/kg body weight doses. A dose dependent percentage tail DNA was recorded in the peripheral blood lymphocyte, liver and bone marrow cells on rats at all the doses tested. The micronucleus and CA tests using bone marrow cells showed the prominent DNA damage potential of NiO-NPs corroborating the comet assay results. Primary interaction of NiO-NPs or nickel ions generated from NiO-NPs and secondary interaction of reactive oxygen species generated in response to NiO-NPs toxic insult with the DNA are the suspected reasons for observed genotoxicity. This study highlights the probability of DNA damaging effects in non-target organisms when exposed to NiO-NPs for a long time. Investigations to elucidate the NiO-NPs mediated adverse effects on terrestrial organisms are warranted.</div></div>","PeriodicalId":20852,"journal":{"name":"Regulatory Toxicology and Pharmacology","volume":"161 ","pages":"Article 105858"},"PeriodicalIF":3.0000,"publicationDate":"2025-05-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Regulatory Toxicology and Pharmacology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0273230025000881","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MEDICINE, LEGAL","Score":null,"Total":0}
引用次数: 0
Abstract
Nanotechnology has revolutionized industrial processing and human life by the applications of nanoparticles (NPs), especially the metal oxide ones. Nickel oxide (NiO) NPs have been used in applications including electronics and biosensors. Occupational and accidental exposure to these NPs for longer durations is apparent and the same may lead to significant health risks. In the present study, we have elucidated the genotoxic ability of NiO-NPs post repeated oral exposure for 28 days in Wistar albino rats at 50, 100, and 200 mg/kg body weight doses. A dose dependent percentage tail DNA was recorded in the peripheral blood lymphocyte, liver and bone marrow cells on rats at all the doses tested. The micronucleus and CA tests using bone marrow cells showed the prominent DNA damage potential of NiO-NPs corroborating the comet assay results. Primary interaction of NiO-NPs or nickel ions generated from NiO-NPs and secondary interaction of reactive oxygen species generated in response to NiO-NPs toxic insult with the DNA are the suspected reasons for observed genotoxicity. This study highlights the probability of DNA damaging effects in non-target organisms when exposed to NiO-NPs for a long time. Investigations to elucidate the NiO-NPs mediated adverse effects on terrestrial organisms are warranted.
期刊介绍:
Regulatory Toxicology and Pharmacology publishes peer reviewed articles that involve the generation, evaluation, and interpretation of experimental animal and human data that are of direct importance and relevance for regulatory authorities with respect to toxicological and pharmacological regulations in society. All peer-reviewed articles that are published should be devoted to improve the protection of human health and environment. Reviews and discussions are welcomed that address legal and/or regulatory decisions with respect to risk assessment and management of toxicological and pharmacological compounds on a scientific basis. It addresses an international readership of scientists, risk assessors and managers, and other professionals active in the field of human and environmental health.
Types of peer-reviewed articles published:
-Original research articles of relevance for regulatory aspects covering aspects including, but not limited to:
1.Factors influencing human sensitivity
2.Exposure science related to risk assessment
3.Alternative toxicological test methods
4.Frameworks for evaluation and integration of data in regulatory evaluations
5.Harmonization across regulatory agencies
6.Read-across methods and evaluations
-Contemporary Reviews on policy related Research issues
-Letters to the Editor
-Guest Editorials (by Invitation)