应用计算机分类模型评价敌敌畏(DDVP)的细胞毒性和致突变性尼日利亚的健康危害意识。

Environmental analysis, health and toxicology Pub Date : 2020-09-01 Epub Date: 2020-09-28 DOI:10.5620/eaht.2020016
Yahaya Abdulwahid Abaukaka, Salihu Sanusi, Kabir Abdullahi Ozigi, Fatima Umar Malo
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引用次数: 4

摘要

敌敌畏(DDVP)在尼日利亚被滥用于自杀企图、局部应用于治疗体外寄生虫感染,以及在农产品上滥用。亚急性浓度暴露于该化合物可通过改变细胞抗氧化防御机制引起不同组织的毒性。本分析旨在系统分析敌敌畏,以评估其细胞毒性和致突变性的潜力,人类脆弱性使用计算机分类模型。DDVP被归类为从基于结构警报的清单中产生的类似化合物类别,使用定量结构-活性关系(QSAR)模型测量对细胞系和动物模型的生物效应。通过分析皮肤致敏、口服/吸入毒性、神经毒性和致突变性等目标终点来评估敌敌畏的细胞毒性和致突变性潜力。敌敌畏显示出中等致敏潜力,在长时间暴露期间可引起皮肤刺激,因为存在与细胞蛋白相互作用并导致降解的二氯乙烯基侧链。在急性口服毒性大鼠模型中,每体重DDVP的50%致死剂量(LD50)在95%置信范围内为26.2 mg/kg,急性吸入毒性大气中50%致死浓度(LC50)估计为14.4 mmol/L。敌敌畏还能抑制神经系统中的乙酰胆碱酯酶,产生烟碱和毒蕈碱症状,如恶心、呕吐、流泪、流涎、心动过缓和呼吸衰竭,可能导致死亡。广泛使用的农药引起弱DNA甲基化,从而抑制启动子位点的基因转录。敌敌畏具有挥发性,因此在长时间接触时会引起口服和吸入毒性,并伴有神经毒性。应鼓励联邦和州立医院进行血清胆碱酯酶血液检查,以调查相关的健康挑战,因为敌敌畏在尼日利亚仍在使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Assessment of the cytotoxic and mutagenic potential of dichlorvos (DDVP) using in silico classification model; a health hazard awareness in Nigeria.

Assessment of the cytotoxic and mutagenic potential of dichlorvos (DDVP) using in silico classification model; a health hazard awareness in Nigeria.

Assessment of the cytotoxic and mutagenic potential of dichlorvos (DDVP) using in silico classification model; a health hazard awareness in Nigeria.

Assessment of the cytotoxic and mutagenic potential of dichlorvos (DDVP) using in silico classification model; a health hazard awareness in Nigeria.
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.
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