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首页> 外文期刊>Investigational new drugs. >Effect of morin on tissue lipid peroxidation and antioxidant status in 1, 2-dimethylhydrazine induced experimental colon carcinogenesis.
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Effect of morin on tissue lipid peroxidation and antioxidant status in 1, 2-dimethylhydrazine induced experimental colon carcinogenesis.

机译:在1,2-二甲基肼诱导的实验性结肠癌发生中,morin对组织脂质过氧化和抗氧化状态的影响。

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摘要

Colon cancer is the third most malignant neoplasm in the world and it remains today an important cause of death, especially in western countries. In this study, we have evaluated the chemopreventive efficacy of morin on tissue lipid peroxidation and antioxidant status, which are used as biomarkers in 1,2-dimethylhydrazine-induced colon carcinogenesis in a rat model. Male Wistar rats were divided into four groups and received high fat diet. Group 1 served as control, groups 2 and 4 were given a daily treatment of morin (50 mg/kg body weight) orally, everyday for a total period of 30 weeks. Groups 3 and 4 were given weekly subcutaneous injections of DMH at a dose of 20 mg/kg body weight in the groin for 15 weeks. Animals were sacrificed at the end of 30 weeks. The liver, intestine, colon and caecum from different groups were subjected to histopathological studies, determination of lipid peroxidation and antioxidant status. Our results showed decreased levels of liver enzymic and non-enzymic antioxidants and increased levels of lipid peroxidation (LPO) products such as tissue thiobarbituricacid substances (TBARS), lipid hydroperoxides (LOOH) and conjugated dienes (CD) in DMH treated rats, which were significantly (P < 0.05) reversed on morin supplementation. Moreover, intestinal, colonic and caecal TBARS, LOOH, CD and also the antioxidants superoxide dismutase (SOD), catalase (CAT), glutathione S-transferase (GST), glutathione peroxidase (GPx), glutathione reductase (GR) and reduced glutathione (GSH) were significantly diminished in DMH treated rats, which were significantly (P < 0.05) elevated on simultaneous morin supplementation. Moreover, enhanced activity of intestinal, colonic and caecal ascorbic acid and alpha-tocopherol levels were also observed in DMH alone treated rats, which were significantly (P < 0.05) reduced on morin supplementation. These results indicate that morin could exert a significant chemopreventive effect on colon carcinogenesis induced by DMH.
机译:结肠癌是世界上第三大恶性肿瘤,今天它仍然是重要的死亡原因,尤其是在西方国家。在这项研究中,我们评估了香兰素对组织脂质过氧化和抗氧化剂状态的化学预防功效,这些化合物被用作大鼠模型中1,2-二甲基肼诱导的结肠癌发生的生物标志物。将雄性Wistar大鼠分成四组并接受高脂饮食。第1组作为对照组,第2和第4组每天口服莫林(50 mg / kg体重),共30周。第3和第4组每周在腹股沟中皮下注射DMH,剂量为20 mg / kg体重,持续15周。 30周结束时处死动物。对不同组的肝,肠,结肠和盲肠进行了组织病理学研究,确定了脂质过氧化作用和抗氧化状态。我们的研究结果表明,DMH治疗的大鼠肝脏中的抗酶和非酶性抗氧化剂水平降低,脂质过氧化(LPO)产物(如组织硫代巴比妥酸酸物质(TBARS),脂质氢过氧化物(LOOH)和共轭二烯(CD))水平升高。补充大麦菊粉后显着(P <0.05)逆转。此外,肠道,结肠和盲肠的TBARS,LOOH,CD以及抗氧化剂超氧化物歧化酶(SOD),过氧化氢酶(CAT),谷胱甘肽S-转移酶(GST),谷胱甘肽过氧化物酶(GPx),谷胱甘肽还原酶(GR)和还原型谷胱甘肽( GSH)在DMH处理的大鼠中显着降低,在同时补充morin时显着(P <0.05)升高。此外,在单独用DMH处理的大鼠中,还观察到肠道,结肠和盲肠抗坏血酸的活性增强,α-生育酚水平升高,在补充mo草素后显着(P <0.05)降低。这些结果表明,morin对DMH诱导的结肠癌发生具有重要的化学预防作用。

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