Villaorduña Carlos, Mendoza-Carlos Mariano, Chuyma Manuel, Avilés Jhon, Avalos-Diaz Ayda, Lozano-Reategui Ronald, Garcia-Ruiz Juan, Panduro-Tenazoa Nadia, Vargas Jessy, Moran-Quintanilla Ysabel, Rodríguez José-Luis
Faculty of Pharmacy, Universidad Nacional Mayor de San Marcos, Lima 15021, Peru.
Agroforestry Department, Universidad Nacional Intercultural de la Amazonia, Pucallpa 25004, Peru.
Toxics. 2023 Jun 30;11(7):566. doi: 10.3390/toxics11070566.
Ipconazole is an antifungal agrochemical widely used in agriculture against seed diseases of rice, vegetables, and other crops; due to its easy accumulation in the environment, it poses a hazard to human, animal, and environmental health. Therefore, we investigated the cytotoxic effect of ipconazole on SH-SY5Y neuroblastoma cells using cell viability tests (MTT), ROS production, caspase3/7 activity, and molecular assays of the biomarkers of cell death (Bax, Casp3, APAF1, BNIP3, and Bcl2); inflammasome (NLRP3, Casp1, and IL1β); inflammation (NFκB, TNFα, and IL6); and antioxidants (NRF2, SOD, and GPx). SH-SY5Y cells were exposed to ipconazole (1, 5, 10, 20, 50, and 100 µM) for 24 h. The ipconazole, in a dose-dependent manner, reduced cell viability and produced an IC of 32.3 µM; it also produced an increase in ROS production and caspase3/7 enzyme activity in SH-SY5Y cells. In addition, ipconazole at 50 µM induced an overexpression of Bax, Casp3, APAF1, and BNIP3 (cell death genes); NLRP3, Casp1, and IL1B (inflammasome complex genes); and NFκB, TNFα, and IL6 (inflammation genes); it also reduced the expression of NRF2, SOD, and GPx (antioxidant genes). Our results show that ipconazole produces cytotoxic effects by reducing cell viability, generating oxidative stress, and inducing cell death in SH-SY5Y cells, so ipconazole exposure should be considered as a factor in the presentation of neurotoxicity or neurodegeneration.
抑霉唑是一种抗真菌农用化学品,广泛应用于农业领域,用于防治水稻、蔬菜和其他作物的种子病害;由于其易于在环境中积累,对人类、动物和环境健康构成危害。因此,我们使用细胞活力测试(MTT)、活性氧生成、半胱天冬酶3/7活性以及细胞死亡生物标志物(Bax、Casp3、APAF1、BNIP3和Bcl2)、炎性小体(NLRP3、Casp1和IL1β)、炎症(NFκB、TNFα和IL6)以及抗氧化剂(NRF2、SOD和GPx)的分子检测方法,研究了抑霉唑对SH-SY5Y神经母细胞瘤细胞的细胞毒性作用。将SH-SY5Y细胞暴露于抑霉唑(1、5、10、20、50和100μM)中24小时。抑霉唑以剂量依赖性方式降低细胞活力,IC50为32.3μM;它还导致SH-SY5Y细胞中的活性氧生成增加和半胱天冬酶3/7酶活性增加。此外,50μM的抑霉唑诱导Bax、Casp3、APAF1和BNIP3(细胞死亡基因)、NLRP3、Casp1和IL1B(炎性小体复合物基因)以及NFκB、TNFα和IL6(炎症基因)的过表达;它还降低了NRF2、SOD和GPx(抗氧化基因)的表达。我们的结果表明,抑霉唑通过降低细胞活力、产生氧化应激和诱导SH-SY5Y细胞死亡而产生细胞毒性作用,因此,应将接触抑霉唑视为神经毒性或神经退行性变表现的一个因素。