Department of Biochemistry and Nutrition, CSIR - Central Food Technological Research Institute (CFTRI), Mysore 570020, Karnataka, India.
Neurotoxicology. 2012 Oct;33(5):1254-64. doi: 10.1016/j.neuro.2012.07.006. Epub 2012 Jul 25.
Acrylamide (ACR) intoxication in its monomeric form leads to neuronal damage in both experimental animals and humans. Oxidative stress is one of the principle mechanisms related to the neurotoxicity of ACR exposure. Hence, the present study aimed to recapitulate the potential of ACR to cause oxidative stress and neurotoxic effects in Drosophila melanogaster. Exposure of adult male flies (Oregon K strain) to ACR (1-10 mM, 7 d) in the diet resulted in a concentration and time dependent mortality, while the survivors exhibited significant locomotor deficits. Further, ACR exposure (1-5 mM, 3 d) caused robust oxidative stress as evidenced by markedly elevated levels of reactive oxygen species and hypdroperoxides in head/body regions. Enhanced lipid peroxidation, perturbations in the activities of antioxidant enzymes accompanied with depletion of reduced glutathione levels in head region at high concentrations suggested induction of oxidative stress. Further, marked diminution in the activities of complexes I-III, Succinic dehydrogenase, with concomitant reduction in MTT suggested the propensity of ACR to impair mitochondrial function. Furthermore, ACR-induced neurotoxic effects were discernible in terms of diminished ATPase activity, enhanced activity of acetylcholinesterase and dopamine depletion. In a satellite study, employing a co-exposure paradigm, we tested the propensity of spice actives namely eugenol (EU) and isoeugenol (IE) to ameliorate ACR-induced neurotoxicity. EU/IE enriched diet offered marked protection against ACR-induced mortality, locomotor dysfunctions and oxidative stress. Furthermore, the spice actives prevented the depletion of reduced GSH levels, maintained the activity of AChE enzyme and dopamine levels in head region. Collectively, these findings clearly demonstrate that ACR induced neurotoxicity in Drosophila may be mediated through oxidative stress mechanisms and the potential of spice actives to abrogate the condition. These data suggest that Drosophila may serve as a suitable model to understand the possible mechanism/s associated with ACR associated neuropathy.
丙烯酰胺(ACR)在其单体形式中毒会导致实验动物和人类的神经元损伤。氧化应激是与 ACR 暴露的神经毒性相关的主要机制之一。因此,本研究旨在模拟 ACR 对黑腹果蝇造成氧化应激和神经毒性的潜在影响。在饮食中暴露于 ACR(1-10mM,7d)的成年雄性果蝇(俄勒冈 K 品系)表现出浓度和时间依赖性死亡率,而幸存的果蝇表现出明显的运动缺陷。此外,ACR 暴露(1-5mM,3d)导致强烈的氧化应激,表现为头部/身体区域中活性氧和过氧化物的水平显著升高。在高浓度下,头部区域中脂质过氧化增强、抗氧化酶活性的改变以及还原型谷胱甘肽水平的消耗表明氧化应激的诱导。此外,复合物 I-III、琥珀酸脱氢酶的活性显著降低,同时 MTT 降低表明 ACR 倾向于损害线粒体功能。此外,通过降低 ATP 酶活性、乙酰胆碱酯酶活性增强和多巴胺耗竭,可发现 ACR 诱导的神经毒性作用。在一项卫星研究中,采用共暴露范式,我们测试了香料活性物质,即丁香酚(EU)和异丁香酚(IE)减轻 ACR 诱导的神经毒性的倾向。EU/IE 富集饮食对 ACR 诱导的死亡率、运动功能障碍和氧化应激有明显的保护作用。此外,香料活性物质防止了还原型 GSH 水平的消耗,维持了头部区域中 AChE 酶和多巴胺的活性。总之,这些发现清楚地表明,ACR 诱导的果蝇神经毒性可能是通过氧化应激机制介导的,香料活性物质有减轻这种情况的潜力。这些数据表明,果蝇可能是一种合适的模型,可用于了解与 ACR 相关神经病变相关的潜在机制。