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中国精品科技期刊2020
马蕾, 郝红伟, 李慧玲, 刘敏, 赵文. 蔷薇红景天低聚原花青素对D-半乳糖诱导小鼠过氧化损伤的拮抗作用[J]. 食品工业科技, 2014, (11): 341-345. DOI: 10.13386/j.issn1002-0306.2014.11.067
引用本文: 马蕾, 郝红伟, 李慧玲, 刘敏, 赵文. 蔷薇红景天低聚原花青素对D-半乳糖诱导小鼠过氧化损伤的拮抗作用[J]. 食品工业科技, 2014, (11): 341-345. DOI: 10.13386/j.issn1002-0306.2014.11.067
MA Lei, HAO Hong-wei, LI Hui-ling, LIU Min, ZHAO Wen. Study on antagonism of antioxidant effect of Rhodiola rosca oligomeric proanthocyanidns in deoxidization on mice induced by D-galactose[J]. Science and Technology of Food Industry, 2014, (11): 341-345. DOI: 10.13386/j.issn1002-0306.2014.11.067
Citation: MA Lei, HAO Hong-wei, LI Hui-ling, LIU Min, ZHAO Wen. Study on antagonism of antioxidant effect of Rhodiola rosca oligomeric proanthocyanidns in deoxidization on mice induced by D-galactose[J]. Science and Technology of Food Industry, 2014, (11): 341-345. DOI: 10.13386/j.issn1002-0306.2014.11.067

蔷薇红景天低聚原花青素对D-半乳糖诱导小鼠过氧化损伤的拮抗作用

Study on antagonism of antioxidant effect of Rhodiola rosca oligomeric proanthocyanidns in deoxidization on mice induced by D-galactose

  • 摘要: 目的:探讨蔷薇红景天低聚原花青素(OPCRR)对D-半乳糖(D-gal)诱导小鼠过氧化损伤的拮抗作用。方法:采用D-半乳糖建立ICR小鼠过氧化模型中灌胃给予受试物连续49d,高、中、低剂量组分别添加蔷薇红景天原花青素320、160、80mg/kg·bw,考察血清和心、肝、脑组织中SOD、GSH、GSH-Px、MDA指标及肝、脑组织中的MAO指标。结果:与模型对照组相比,一定剂量的OPCRR可显著提高小鼠血清、心、肝、脑组织中SOD、GSH-Px活性,并显著降低MDA含量,且在高剂量组表现最突出;高剂量组血清、心、肝和脑组织中SOD活力分别增加了29.5%、28.1%、62.7%和90.8%,GSH-Px活性分别增加了67.8%、58.4%、32.1%和50.3%,MDA含量分别降低了19.2%、30.0%、33.3%和19.2%。此外,中、高剂量组极显著降低脑组织MAO活力(p<0.01),分别降低了22.3%和28.6%;高剂量组显著降低肝脏MAO活力(p<0.05),降低了36.5%。结论:OPCRR可一定程度地保护机体,拮抗D-gal的过氧化损伤,预防衰老。 

     

    Abstract: Objective: To investigate the antioxidant effect of Rhodiola rosca oligomeric proantho cyanidns ( OPCRR) in the aged mice induced by D-galactoseactose.Method: Via the process of establishing oxidative damage model by hypodermic injection of D- galactose, OPCRR of different doses ( high dose: 320mg /kg·bw、middle dose: 160mg /kg·bw、low dose: 80 mg /kg·bw) were orally given to mice at the same time for consecutive 49d.The level of SOD, GSH-Px, MDA in mouse serum and organs, and senescent-related enzyme ( MAO) in mouse brain and liver were investigated in peroxide damaged mice in the experiment of the antioxidant activity in vivo.Results: Compared with model control group, a dose of OPCRR could significantly increase SOD, GSH-Px activity of serum, heart, liver and brain, and significantly decrease MDA level, while highest dose had superior effert; high dose group had increased SOD level of serum, heart, liver and brain by 29.5%, 29.5%, 62.7% and 90.8%, while GSH-Px activity had increased 67.8%, 58.4%, 32.1% and 50.3%, and the MDA content was decreased by 19.2%, 30.0%, 33.3% and19.2%. In addition, the middle and high dose group significantly decreased MAO activity of brain ( p < 0.01) by22.3% and 28.6%; High dose group was significantly decreased MAO level of liver ( p < 0.05) by 36.5%.Conclusion:OPCRR's effect on antagonizing D- galactoseactose- induced peroxidative damage was confirmed, and had a degree of ability of preventing oxidation and senescence.

     

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