Stevens T M, Boswell G A, Adler R, Ackerman N R, Kerr J S
Medical Products Department, E. I. du Pont de Nemours & Company, Inc., Wilmington, Delaware 19898.
Toxicol Appl Pharmacol. 1988 Oct;96(1):33-42. doi: 10.1016/0041-008x(88)90244-x.
Oxygen free radicals have the potential to mediate cell injury. Defenses against such radicals include the antioxidant enzymes superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GSH-PX). The purposes of this study were (1) to develop an in vitro model using human cells in which to investigate a potential pharmacologic agent as an inducer of these antioxidant enzymes; (2) to investigate the phenylurea derivative N-[2-(2-oxo-1-imidazolindinyl)ethyl]-N-phenylurea (EDU) in this model with paraquat (PQ) serving as the positive control; and (3) to determine if induction of the antioxidant enzymes by EDU occurs in vivo. Human gingival fibroblasts (Gin-1) were used as the target cell in vitro; PQ and EDU, an inducer of SOD and CAT activities in plants, were evaluated as antioxidant enzyme inducers. Total SOD activity in Gin-1 cells increased 2-fold (p less than 0.05) in the presence of 1.0 mM PQ for 18-48 hr compared with untreated controls. Gin-1 cells incubated with 0.25-2.0 mM PQ for 24 hr had significantly increased total SOD (1.5 to 2.0-fold; p less than 0.05). CAT activity increased with 1.0 and 2.0 mM PQ (p less than 0.05). In the presence of PQ, GSH-PX activity decreased (p less than 0.05) in a concentration-dependent manner, indicating inactivation of this enzyme. No toxicity, indicated by lactate dehydrogenase released into the incubation medium, was noted at PQ concentrations below 5.0 mM. In the presence of 0.125-2.0 mM EDU, total SOD activity in Gin-1 cells significantly increased (1.5 to 2.0-fold; p less than 0.05). CAT activity significantly increased in a dose-dependent manner (p less than 0.05), while GSH-PX activity remained constant following exposure to 0.125-2.0 mM EDU. Intraperitoneal administration of EDU to rats twice a day for 2 days at 100 mg/kg induced SOD activity in heart, liver, and lung compared to controls (p less than 0.05). CAT activity increased in the liver 56% and in the lung 36% (p less than 0.05). GSH-PX activity remained constant. Our findings indicate that Gin-1 cells are a useful model in which to study inducers of antioxidant enzymes in vitro and that the phenylurea compound EDU induces SOD and CAT activities both in vitro and in vivo.
氧自由基有介导细胞损伤的可能。针对此类自由基的防御机制包括抗氧化酶超氧化物歧化酶(SOD)、过氧化氢酶(CAT)和谷胱甘肽过氧化物酶(GSH-PX)。本研究的目的是:(1)建立一种使用人类细胞的体外模型,用以研究一种潜在的药理剂作为这些抗氧化酶的诱导剂;(2)在该模型中研究苯基脲衍生物N-[2-(2-氧代-1-咪唑啉基)乙基]-N-苯基脲(EDU),以百草枯(PQ)作为阳性对照;(3)确定EDU在体内是否能诱导抗氧化酶。人类牙龈成纤维细胞(Gin-1)被用作体外靶细胞;PQ和EDU(一种植物中SOD和CAT活性的诱导剂)被评估为抗氧化酶诱导剂。与未处理的对照相比,在1.0 mM PQ存在下培养18 - 48小时,Gin-1细胞中的总SOD活性增加了2倍(p < 0.05)。用0.25 - 2.0 mM PQ孵育Gin-1细胞24小时,总SOD显著增加(1.5至2.0倍;p < 0.05)。CAT活性在1.0和2.0 mM PQ作用下增加(p < 0.05)。在PQ存在下,GSH-PX活性以浓度依赖方式降低(p < 0.05),表明该酶失活。在PQ浓度低于5.0 mM时,未观察到释放到孵育培养基中的乳酸脱氢酶所指示的毒性。在0.125 - 2.0 mM EDU存在下,Gin-1细胞中的总SOD活性显著增加(1.5至2.0倍;p < 0.05)。CAT活性以剂量依赖方式显著增加(p < 0.05),而在暴露于0.125 - 2.0 mM EDU后,GSH-PX活性保持不变。以100 mg/kg的剂量每天给大鼠腹腔注射EDU两次,持续2天,与对照组相比,心脏、肝脏和肺中的SOD活性增加(p < 0.05)。肝脏中的CAT活性增加了56%,肺中的增加了36%(p < 0.05)。GSH-PX活性保持不变。我们的研究结果表明,Gin-1细胞是体外研究抗氧化酶诱导剂的有用模型,并且苯基脲化合物EDU在体外和体内均能诱导SOD和CAT活性。