Laboratório de Fisiopatologia Experimental, Universidade do Extremo Sul Catarinense, CEP 88806-000, Criciúma, SC, Brazil.
Environ Toxicol Pharmacol. 2007 Mar;23(2):198-204. doi: 10.1016/j.etap.2006.09.003. Epub 2006 Oct 5.
Malathion is an insecticide of the group of organophosphate pesticides (OPs), which shows strong insecticidal effects. However, it possesses mutagenic and carcinogenic properties and shows organ-specific toxicity in relation to the heart, kidney and other vertebrate organs. The exact mechanism of the genotoxic effects of malathion is not yet known. Free radical damage is an important direct or indirect factor in several pathological and toxicological processes, including malathion poisoning. The aim of the present study was the evaluation of oxidative damage in different tissues of Wistar rats, administered intra peritoneally at doses of 25, 50, 100 and 150mgmalathion/kg, after acute and sub-chronic malathion exposure. Oxidative stress evaluation was based on lipid peroxidation by levels of thiobarbituric acid reactive substances (TBARS), protein oxidation by levels of carbonyl groups, and also on the activities of superoxide dismutase and catalase, two antioxidant enzymes that detoxity superoxide radical (O(2)(-)) and hydrogen peroxide, respectively. The results showed that the most sensitive targets of oxidative damage were kidney, lung and diaphragm after acute treatment, and liver, quadriceps and serum after sub-chronic treatment. Also, in general, increased lipid peroxidation measured as TBARS levels seems to be a better biomarker of oxidative stress compared to the contents of protein carbonyls after acute and sub-chronic malathion treatments. The present findings reinforce the concept that oxidative stress and particularly lipoperoxidation, are involved in OPs toxicity.
马拉硫磷是有机磷杀虫剂(OPs)的一种,具有很强的杀虫效果。然而,它具有致突变性和致癌性,并对心脏、肾脏和其他脊椎动物器官具有器官特异性毒性。马拉硫磷的遗传毒性作用的确切机制尚不清楚。自由基损伤是包括马拉硫磷中毒在内的几种病理和毒理学过程中的一个重要直接或间接因素。本研究的目的是评价急性和亚慢性马拉硫磷暴露后,不同组织中 Wistar 大鼠的氧化损伤。通过测定硫代巴比妥酸反应物质(TBARS)水平评估脂质过氧化,通过测定羰基含量评估蛋白质氧化,同时测定超氧化物歧化酶和过氧化氢酶的活性,这两种抗氧化酶分别解毒超氧自由基(O2(-))和过氧化氢。结果表明,急性处理后,肾脏、肺和横膈膜是最敏感的氧化损伤靶标,而亚慢性处理后,肝脏、四头肌和血清是最敏感的靶标。此外,一般来说,与急性和亚慢性马拉硫磷处理后的蛋白质羰基含量相比,TBARS 水平升高似乎是氧化应激的更好生物标志物。本研究结果进一步证实了氧化应激,特别是脂质过氧化,参与了有机磷的毒性。