Venturini F P, de Moraes F D, Rossi P A, Avilez I M, Shiogiri N S, Moraes G
Nanomedicine and Nanotoxicology Group, Physics Institute of São Carlos, University of São Paulo, Avenida Trabalhador Sãocarlense, 400, São Carlos, SP, 13560-970, Brazil.
Department of Genetics and Evolution, Federal University of Sao Carlos, Rodovia Washington Luiz, Km 235, Sao Carlos, SP, CEP 13565-905, Brazil.
Fish Physiol Biochem. 2019 Feb;45(1):341-353. doi: 10.1007/s10695-018-0566-1. Epub 2018 Sep 30.
Effects of the pyrethroid lambda-cyhalothrin (LCH) were investigated in matrinxa Brycon amazonicus, a non-target freshwater teleost. The fish were submitted to a single-pulse exposure (10% of LC50; 96 h, 0.65 μg L), followed by 7 days of recovery in clean water. Hematologic parameters indicated impairments in oxygen transport, which were not recovered. Plasma [Na], [Cl], and protein were diminished, and only [Na] remained low after recovery. Gill Na/KATPase activity was increased and recovered to basal values. Brain acetylcholinesterase activity was not responsive to LCH. Liver ascorbic acid concentration was not altered, and reduced glutathione levels remained augmented even after recovery. LCH inhibited hepatic superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPx) activities, while glutathione-S-transferase (GST) and glucose-6-phosphate dehydrogenase (G6PDH) activities were steady. After recovery, SOD remained low, and GPx was augmented. Liver depicted lipid peroxidation, which was not observed after recovery. Hepatic morphology was affected by LCH and was not completely recovered. These responses, combined with the persistence of changes even after recovery span, clearly show the feasibility of these biomarkers in evaluating LCH toxic potential to non-target organisms, highlighting the importance of pyrethroids' responsible use.
研究了拟除虫菊酯高效氯氟氰菊酯(LCH)对非靶标淡水硬骨鱼亚马孙脂鲤的影响。将鱼进行单次脉冲暴露(LC50的10%;96小时,0.65μg/L),随后在清洁水中恢复7天。血液学参数表明氧气运输受损,且未恢复。血浆中的[Na]、[Cl]和蛋白质减少,恢复后只有[Na]仍处于低水平。鳃Na/KATP酶活性增加并恢复到基础值。脑乙酰胆碱酯酶活性对LCH无反应。肝脏抗坏血酸浓度未改变,即使恢复后还原型谷胱甘肽水平仍升高。LCH抑制肝脏超氧化物歧化酶(SOD)、过氧化氢酶(CAT)和谷胱甘肽过氧化物酶(GPx)的活性,而谷胱甘肽-S-转移酶(GST)和葡萄糖-6-磷酸脱氢酶(G6PDH)的活性稳定。恢复后,SOD仍处于低水平,而GPx升高。肝脏出现脂质过氧化,恢复后未观察到。肝脏形态受到LCH的影响,且未完全恢复。这些反应,再加上即使在恢复期后变化仍持续存在,清楚地表明了这些生物标志物在评估LCH对非靶标生物的潜在毒性方面的可行性,突出了合理使用拟除虫菊酯的重要性。