Kumar O, Lakshmana Rao P V, Pradhan S, Jayaraj R, Bhaskar A S B, Nashikkar A B, Vijayaraghavan R
Division of Pharmacology and Toxicology, Defence Research and Development Establishment, Gwalior, India.
Cell Mol Biol (Noisy-le-grand). 2007 May 30;53(5):92-102.
Ricin a glycoprotein from the Ricinus communis seeds, is known to have diverse toxic effects on cells of different visceral organs. We have studied the effect of ricin (0.5, 1.0 and 2.0 LD50) on various oxidative stress markers at 1, 3 and 7 day post exposure following i.p. administration in Swiss albino male mice. Results of this study revealed that ricin induces generation of reactive species, lipidperoxidation, DNA fragmentation and depletion of GSH. Activity of antioxidant cascade related enzyme like superoxide dismutase (SOD), glutathione peroxidase (GPx) decreased, while glutathione reductase (GR) and catalase activity increased. Superoxide dismutase and glutathione peroxidase activity was decreased significantly in liver, spleen and kidney. The decrease was more prominent on 7 day of post exposure in all the exposed doses. A significant increase in the activities of catalase was observed in plasma, liver, spleen and kidney on 7 day following ricin exposure. Glutathione reductase increased significantly as early as 24 h following 1.0 LD50 dose. Lipid peroxidation increased and non protein sulfhydryl content decreased in all the tissues at different time intervals. Total antioxidant status was reduced as early as 1 day post exposure. Nearly two fold increase was observed in DNA fragmentation following 0.5 LD50 dose of ricin on 1 day post exposure. DNA diffusion assay also indicated an early damage to DNA due to ROS. An early change in DNA fragmentation, DNA diffusion, and total antioxidant status and in the activity of various enzymes indicates that ricin produce oxidative stress by generation of reactive oxygen species as early as 24 h at a minimum dose of 0.5 LD50. Probably this is the first study which indicate that ricin induced oxidative stress at a minimum dose of 0.5 LD50.
蓖麻毒素是一种来自蓖麻种子的糖蛋白,已知对不同内脏器官的细胞具有多种毒性作用。我们研究了在瑞士白化雄性小鼠腹腔注射后,1、3和7天暴露期时,蓖麻毒素(0.5、1.0和2.0 LD50)对各种氧化应激标志物的影响。这项研究的结果表明,蓖麻毒素可诱导活性物质生成、脂质过氧化、DNA片段化以及谷胱甘肽(GSH)耗竭。超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GPx)等抗氧化级联相关酶的活性降低,而谷胱甘肽还原酶(GR)和过氧化氢酶活性增加。肝脏、脾脏和肾脏中的超氧化物歧化酶和谷胱甘肽过氧化物酶活性显著降低。在所有暴露剂量下,暴露后7天这种降低更为明显。蓖麻毒素暴露7天后,血浆、肝脏、脾脏和肾脏中过氧化氢酶活性显著增加。在1.0 LD50剂量后24小时,谷胱甘肽还原酶就显著增加。在不同时间间隔,所有组织中的脂质过氧化增加,非蛋白巯基含量降低。暴露后1天,总抗氧化状态就开始降低。在暴露后1天,0.5 LD50剂量的蓖麻毒素使DNA片段化增加了近两倍。DNA扩散试验也表明,活性氧(ROS)会导致DNA早期损伤。DNA片段化、DNA扩散、总抗氧化状态以及各种酶活性的早期变化表明,蓖麻毒素在最低剂量0.5 LD50时,最早在24小时就通过产生活性氧来产生氧化应激。这可能是第一项表明蓖麻毒素在最低剂量0.5 LD50时诱导氧化应激的研究。