氧化应激
神经毒性
超氧化物歧化酶
DNA损伤
活性氧
过氧化氢酶
黑腹果蝇
脂质过氧化
抗氧化剂
化学
基因敲除
生物化学
细胞凋亡
生物
细胞生物学
药理学
毒性
DNA
基因
有机化学
作者
Shilpa Olakkaran,Kizhakke Purayil Anupama,Anet Antony,Hunasanahally Puttaswamygowda Gurushankara
出处
期刊:Toxicology
[Elsevier BV]
日期:2021-09-21
卷期号:462: 152959-152959
被引量:77
标识
DOI:10.1016/j.tox.2021.152959
摘要
The widespread use of lead (Pb) has caused global contamination, inevitable human exposure, and public health problems. Pb neurotoxicity has been linked to various human diseases, but its associated mechanism causing neurotoxicity is unknown. Drosophila melanogaster as a model organism has been used to study the mechanism involved in Pb-caused neurotoxicity and the potential role of antioxidants in ameliorating its harmful effects. The larval feeding technique was adopted to administer different concentrations of Pb (0.2-0.8 mM) to Oregon-R (ORR), superoxide dismutase (Sod), or catalase (Cat) overexpressing, and Sod or Cat knockdown flies to analyse Pb load, oxidative stress components, DNA damage, apoptosis and vacuolation in the brain. The results revealed that Pb accumulation in the Drosophila brain induces oxidative stress by generating reactive oxygen species (ROS) and lipid peroxidation (LPO), depleting antioxidant enzymes. Molecular docking studies have evidenced it. Pb directly binds to antioxidants and major grooves of DNA, leading to DNA damage. Increased DNA damage, apoptosis, vacuolation in brains of Pb-treated ORR, Sod, or Cat knockdown flies; and on the contrary, reduced oxidative DNA damage, apoptosis, and vacuolation in brains of Pb treated Sod or Cat overexpressed flies put forward that oxidative stress is the mechanism in Pb caused neurotoxicity.
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