Endocrinology and Metabolism Research Center, Institute of Basic and Clinical Physiology Sciences, Kerman, Iran.
Department of Clinical Biochemistry, School of Medicine, 48463Kerman University of Medical Sciences, Kerman, Iran.
Toxicol Ind Health. 2022 Nov;38(11):717-732. doi: 10.1177/07482337221125954. Epub 2022 Sep 30.
In this study, oxidative stress was investigated as the possible mechanism of action of organochlorine pesticides (OCPs) and organophosphorus pesticides (OPPs) in primary brain tumors (PBT). The levels of seven OCP residues and enzymatic antioxidant biomarkers including erythrocyte acetylcholinesterase (AChE), superoxide dismutase (SOD), glutathione peroxidase (GPx), catalase (CAT), and paraoxonase-1 (PON-1) along with non-enzymatic oxidative biomarkers including malondialdehyde (MDA), protein carbonyl (PC), total antioxidant capacity (TAC), and nitric oxide (NO) were measured in blood samples of 73 patients with PBT and 104 healthy controls. A significant association was found between farming activities and PBT (55% of patients were engaged in farming activities while 45% had no farming experience). The mean levels of β-HCH, γ-HCH, 2,4 DDE, 4,4 DDE, 4,4 DDT, MDA, PC, NO, SOD, CAT, and GPx were significantly higher in PBT patients, whereas the levels of TAC, PON-1, and AChE were significantly lower in these patients. Regression analysis showed that PBT was correlated with β-HCH, γ-HCH, 2,4 DDE, 4,4 DDE, and 4,4 DDT. Based on these results, it can be concluded that OCPs and OPPs may play a role in PBT development through the formation of reactive oxygen species (ROS) and promoting oxidative stress.
在这项研究中,研究了氧化应激是否是有机氯农药 (OCPs) 和有机磷农药 (OPPs) 在原发性脑肿瘤 (PBT) 中作用的可能机制。测量了 73 名 PBT 患者和 104 名健康对照者血液样本中的 7 种 OCP 残留水平和酶抗氧化生物标志物,包括红细胞乙酰胆碱酯酶 (AChE)、超氧化物歧化酶 (SOD)、谷胱甘肽过氧化物酶 (GPx)、过氧化氢酶 (CAT) 和对氧磷酶-1 (PON-1),以及非酶氧化生物标志物,包括丙二醛 (MDA)、蛋白羰基 (PC)、总抗氧化能力 (TAC) 和一氧化氮 (NO)。研究发现,与 PBT 之间存在显著关联,55%的患者从事农业活动,而 45%的患者没有农业经验。β-HCH、γ-HCH、2,4 DDE、4,4 DDE、4,4 DDT、MDA、PC、NO、SOD、CAT 和 GPx 的平均水平在 PBT 患者中显著升高,而 TAC、PON-1 和 AChE 的水平在这些患者中显著降低。回归分析表明,PBT 与β-HCH、γ-HCH、2,4 DDE、4,4 DDE 和 4,4 DDT 有关。基于这些结果,可以得出结论,OCPs 和 OPPs 可能通过形成活性氧 (ROS) 和促进氧化应激在 PBT 发展中发挥作用。