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刘重斌, 肖敏, 吴博. 硝苯地平对铁负荷大鼠营养代谢影响[J]. 中国公共卫生, 2010, 26(11): 1402-1404. DOI: 10.11847/zgggws2010-26-11-29
引用本文: 刘重斌, 肖敏, 吴博. 硝苯地平对铁负荷大鼠营养代谢影响[J]. 中国公共卫生, 2010, 26(11): 1402-1404. DOI: 10.11847/zgggws2010-26-11-29
LIU Chong-bin, XIAO Min, WU Bo. Effects of nifedipine on nutritional metabolism of iron overload rats[J]. Chinese Journal of Public Health, 2010, 26(11): 1402-1404. DOI: 10.11847/zgggws2010-26-11-29
Citation: LIU Chong-bin, XIAO Min, WU Bo. Effects of nifedipine on nutritional metabolism of iron overload rats[J]. Chinese Journal of Public Health, 2010, 26(11): 1402-1404. DOI: 10.11847/zgggws2010-26-11-29

硝苯地平对铁负荷大鼠营养代谢影响

Effects of nifedipine on nutritional metabolism of iron overload rats

  • 摘要: 目的探讨硝苯地平对铁负荷大鼠营养代谢的影响。方法 30只SD大鼠随机分为对照组、铁负荷组、硝苯地平组(连续7 d腹腔注射硝苯地平),测定血脂、脂质过氧化指标、血清中铁、钙、锌,以及铁蛋白和维生素E含量。结果硝苯地平组大鼠总胆固醇(TC)、低密度脂蛋白(LDL)分别为1.65、0.96 mmol/L,明显低于铁负荷组1.91,1.14 mmol/L,(P<0.05);血清中铁、铁蛋白分别为(1.321±0.148)mg/L,明显低于铁负荷组(1.573±0.253)mg/L(P<0.01),硒含量为(0.087±0.017)mg/L,高于铁负荷组(0.074±0.012)mg/L(P<0.05)。结论硝苯地平影响铁负荷大鼠的营养代谢,降低铁负荷对机体的损害。

     

    Abstract: ObjectiveTo study the effects of nifedipine on nutritional metabolism of iron overload rats.MethodsThirty male SD rats were randomly divided into 3 groups according to their weight(control,iron overload and nifedipine group).Rats in nifedipine group were treated with peritoneal injection of nifedipine for 7 days continuously.The levels of blood lipid,lipid peroxidation indexes,activities of antioxidant enzymes and contents of serum Fe,ferritin,VE,Fe,Se,and Ca were determined.ResultsThe total cholesterol and low-density lipopotein in rats of nifedipine group were 1.65 and 0.96 mmol/L,and significantly lower than those of rats of iron overload(P<0.05).And at the same time,the contents of serum Fe and ferritin were 1.321±0.148 and 1.386±0.162 mg/L,and significantly lower than those of to the iron overload group.But the contents of serum Se in rats of nifedipine group was 0.087±0.017 mg/L and significantly higher than that of the iron overload group.ConclusionNifedipine can alter the nutritional metabolism and decrease the impact of iron overload in rats.

     

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