Sauer Elisa, Moro Angela M, Brucker Natália, Nascimento Sabrina, Gauer Bruna, Fracasso Rafael, Gioda Adriana, Beck Ruy, Moreira José C F, Eifler-Lima Vera Lucia, Garcia Solange Cristina
Laboratory of Toxicology (LATOX), Department of Clinical and Toxicology Analysis, Federal University of Rio Grande do Sul, Porto Alegre, RS 90610000, Brazil.
Department of Chemistry, Pontifical Catholic University of Rio de Janeiro (PUC-Rio), Rio de Janeiro, RJ 22453900, Brazil.
Int J Environ Res Public Health. 2014 Nov 13;11(11):11676-90. doi: 10.3390/ijerph111111676.
Neonicotinoids represent the most used class of insecticides worldwide, and their precursor, imidacloprid, is the most widely marketed. The aim of this study was to evaluate the effect of imidacloprid on the activity of hepatic δ-aminolevulinate dehydratase (δ-ALA-D), protective effect of potential antioxidants against this potential effect and presence of chemical elements in the constitution of this pesticide. We observed that δ-ALA-D activity was significantly inhibited by imidacloprid at all concentrations tested in a dose-dependent manner. The IC50 value was obtained and used to evaluate the restoration of the enzymatic activity. δ-ALA-D inhibition was completely restored by addition of dithiotreitol (DTT) and partly by ZnCl2, demonstrating that the inhibition occurs by oxidation of thiol groups and by displacement of the Zn (II), which can be explained by the presence of chemical elements found in the constitution of pesticides. Reduced glutathione (GSH) had the best antioxidant effect against to δ-ALA-D inhibition caused by imidacloprid, followed by curcumin and resveratrol. It is well known that inhibition of the enzyme δ-ALA-D may result in accumulation of its neurotoxic substrate (δ-ALA), in this line, our results suggest that further studies are needed to investigate the possible neurotoxicity induced by neonicotinoids and the involvement of antioxidants in cases of poisoning by neonicotinoids.
新烟碱类是全球使用最广泛的一类杀虫剂,其前体吡虫啉是市场上销售最广的。本研究的目的是评估吡虫啉对肝脏δ-氨基乙酰丙酸脱水酶(δ-ALA-D)活性的影响、潜在抗氧化剂对这种潜在影响的保护作用以及该农药成分中化学元素的存在情况。我们观察到,在所有测试浓度下,吡虫啉均以剂量依赖的方式显著抑制δ-ALA-D活性。获得了IC50值并用于评估酶活性的恢复情况。加入二硫苏糖醇(DTT)可完全恢复δ-ALA-D的抑制作用,加入氯化锌(ZnCl2)可部分恢复,这表明抑制作用是通过硫醇基团的氧化和锌(II)的取代而发生的,这可以用农药成分中发现的化学元素来解释。还原型谷胱甘肽(GSH)对吡虫啉引起的δ-ALA-D抑制具有最佳的抗氧化作用,其次是姜黄素和白藜芦醇。众所周知,抑制δ-ALA-D酶可能导致其神经毒性底物(δ-ALA)的积累,据此,我们的结果表明需要进一步研究以调查新烟碱类可能诱导的神经毒性以及抗氧化剂在新烟碱类中毒病例中的作用。