{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,3]],"date-time":"2026-06-03T00:32:37Z","timestamp":1780446757494,"version":"3.54.1"},"reference-count":68,"publisher":"The Korean Society of Environmental Health and Toxicology","issue":"3","license":[{"start":{"date-parts":[[2020,9,28]],"date-time":"2020-09-28T00:00:00Z","timestamp":1601251200000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"}],"content-domain":{"domain":["eaht.org"],"crossmark-restriction":true},"short-container-title":["Environ Anal Health Toxicol"],"abstract":"<jats:p>Dichlorvos (DDVP) has been abused in Nigeria for suicide attempts, topical applications to treat an ectoparasitic infestation, and indiscriminate use on farm produce. Exposure to this compound in subacute concentration can cause toxicity in different tissues by alteration of the cellular antioxidative defence mechanism. This analysis is aimed at the systematic profiling of DDVP to assess its cytotoxic and mutagenic potential for human vulnerability using an in silico classification model. DDVP was grouped into categories of analogue chemical compounds generated from inventories based on structural alerts that measure the biological effects on cell lines and animal models using the quantitative structure-activity relationship (QSAR) model. The cytotoxic and mutagenic potential of DDVP was assessed by analyzing target endpoints like skin sensitization, oral\/inhalation toxicity, neurotoxicity and mutagenicity. DDVP shows moderate sensitization potential that can induce skin irritation during prolonged exposure because of the presence of dichlorovenyl side-chain that interacts with cellular proteins and causes degradation. 50% lethal dose (LD50) of DDVP per body weight was determined to be 26.2 mg\/kg in a rat model at 95% confidence range for acute oral toxicity, and 14.4 mmol\/L was estimated as 50% lethal concentration (LC50) in the atmosphere due to acute inhalation toxicity. DDVP can also inhibit acetylcholinesterase in the nervous system to produce nicotinic and muscarinic symptoms like nausea, vomiting, lacrimation, salivation, bradycardia, and respiratory failure may cause death. The widely used pesticide causes weak DNA methylation which can repress gene transcription on promoter sites. DDVP is volatile so it can cause oral and inhalation toxicity coupled with neurotoxicity during prolonged exposure. Serum cholinesterase blood tests should be encouraged in federal and state hospitals to investigate related health challenges as DDVP is still used in Nigeria.<\/jats:p>","DOI":"10.5620\/eaht.2020016","type":"journal-article","created":{"date-parts":[[2020,9,27]],"date-time":"2020-09-27T23:13:26Z","timestamp":1601248406000},"page":"e2020016","update-policy":"https:\/\/doi.org\/10.5620\/crossmark_policy","source":"Crossref","is-referenced-by-count":4,"title":["Assessment of the cytotoxic and mutagenic potential of dichlorvos (DDVP) using in silico classification model; a health hazard awareness in Nigeria"],"prefix":"10.5620","volume":"35","author":[{"given":"Yahaya Abdulwahid","family":"Abaukaka","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Salihu","family":"Sanusi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kabir Abdullahi","family":"Ozigi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Fatima Umar","family":"Malo","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"3578","published-online":{"date-parts":[[2020,9,28]]},"reference":[{"key":"ref1","doi-asserted-by":"publisher","DOI":"10.1016\/B978-012088523-7\/50003-X"},{"key":"ref2","doi-asserted-by":"publisher","DOI":"10.1080\/09603123.2016.1268679"},{"key":"ref3","first-page":"155","volume-title":"Nerve agents","author":"Sidell","year":"2008"},{"key":"ref4","doi-asserted-by":"publisher","DOI":"10.2165\/00139709-200524010-00003"},{"key":"ref5","doi-asserted-by":"publisher","DOI":"10.2165\/00139709-200625010-00001"},{"key":"ref6","doi-asserted-by":"publisher","DOI":"10.1016\/j.scitotenv.2018.08.286"},{"key":"ref7","doi-asserted-by":"publisher","DOI":"10.1080\/109374099281205"},{"key":"ref8","doi-asserted-by":"publisher","DOI":"10.1016\/j.taap.2018.06.004"},{"key":"ref9","doi-asserted-by":"publisher","DOI":"10.1080\/10643389.2019.1565554"},{"key":"ref10","doi-asserted-by":"publisher","DOI":"10.1016\/j.cbi.2016.11.027"},{"key":"ref11","doi-asserted-by":"publisher","DOI":"10.1016\/B978-0-444-62627-1.00010-X"},{"key":"ref12","doi-asserted-by":"publisher","DOI":"10.1177\/0960327116680273"},{"key":"ref13","first-page":"14270","volume-title":"Acetylcholinesterase. 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