多氯联苯(PCBs)诱导的氧化应激对雄性Wistar大鼠椎体抗氧化系统的影响:维生素C和E的改善作用

Subramanian Karthikeyan, Muthusamy Sridhar, Govindan Ramajayam, Ramadoss Lavanya, Jagadeesan Arunakaran, Narasimhan Srinivasan
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引用次数: 2

摘要

尽管PCB在许多国家已经被禁止了几十年,但它在环境中仍然普遍存在,对包括骨骼在内的各种器官系统有广泛的不利影响。本研究旨在评估多氯联苯对成年雄性Wistar大鼠椎骨的影响以及维生素C或E的改善作用。ⅰ组大鼠腹腔灌胃玉米油,ⅱ组大鼠灌胃Aroclor [1254] 2 mg/kg bwt/d (i.p),ⅲ组大鼠灌胃Aroclor [1254] 1 mg/kg bwt/d同时灌胃维生素C 100 mg/kg bwt/d(口服),ⅳ组大鼠灌胃Aroclor [1254] 1 mg/kg bwt/d同时灌胃维生素E 50 mg/kg bwt/d(口服)。30天后,对大鼠实施安乐死并解剖椎骨。测定对照动物和实验动物椎骨中成骨细胞功能标志物(ALP、Collagen)、破骨细胞功能标志物(TRAP)、抗氧化酶(SOD、GPx、GST)和脂质过氧化(LPO)水平。多氯联苯(Aroclor 1254)处理后大鼠ALP、胶原酶活性显著降低,TRAP活性显著升高。多氯联苯处理大鼠SOD和GPx均升高。与多氯联苯同时给予维生素C或E,可阻止多氯联苯对ALP和TRAP的影响。同时给予维生素C处理组GST活性有效。PCB处理改变了LPO,其余动物没有改变。多氯联苯诱导氧化应激,刺激破骨细胞活性,但抑制成骨细胞功能,扰乱抗氧化系统。维生素C或维生素E能够防止多氯联苯的影响。
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Polychlorinated biphenyl (PCBs)-induced oxidative stress plays a role on vertebral antioxidant system: Ameliorative role of vitamin C and E in male Wistar rats

PCB are still prevalent in the environment despite the fact that they have been banned in many countries for several decades, have wide range of adverse effects in various organ systems including bone. The present study aimed at evaluating the effects of PCB on vertebral bone and the ameliorative role of vitamin C or E in the adult male Wistar rats. Group-I rats received vehicle (corn oil) intraperitoneally (i.p), group-II received Aroclor [1254] 2 mg/kg bwt/day (i.p), group-III received Aroclor [1254] (i.p) and simultaneously vitamin C 100 mg/kg bwt/day (orally), group-IV received Aroclor [1254] (i.p) and simultaneously vitamin E 50 mg/kg bwt/day (orally). After 30 days, rats were euthanized and vertebrae were dissected. The osteoblast functional markers (ALP and Collagen), osteoclast functional marker (TRAP), antioxidant enzymes (SOD, GPx and GST) and lipid peroxidation (LPO) were assessed in the vertebral bone of control and experimental animals. A significant decrease the ALP, collagen enzyme activity and increase the TRAP activity were observed in PCBs (Aroclor 1254) treated rats. SOD and GPx were increased in the PCB treated rats. Vitamin C or E given along with PCB, prevented the effects of PCB on ALP and TRAP. GST activity was effective in simultaneous administration of vitamin C treated group. LPO was altered in PCB treatment and animals remaining were not altered. PCB induces oxidative stress and stimulates osteoclast activity but suppresses osteoblast function and it perturbs the antioxidant system. Vitamin C or vitamin E was able to prevent the effects of PCB.

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