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李晓红, 贺圣文, 谭金峰, 王飞, 李万伟. PM2.5致大鼠肺氧化应激损伤及硫辛酸保护作用[J]. 中国公共卫生, 2018, 34(12): 1646-1649. DOI: 10.11847/zgggws1119847
引用本文: 李晓红, 贺圣文, 谭金峰, 王飞, 李万伟. PM2.5致大鼠肺氧化应激损伤及硫辛酸保护作用[J]. 中国公共卫生, 2018, 34(12): 1646-1649. DOI: 10.11847/zgggws1119847
Xiao-hong LI, Sheng-wen HE, Jin-feng TAN, . PM2.5 induced lung oxidative stress injury and protective effect of lipoic acid against the injury in rats[J]. Chinese Journal of Public Health, 2018, 34(12): 1646-1649. DOI: 10.11847/zgggws1119847
Citation: Xiao-hong LI, Sheng-wen HE, Jin-feng TAN, . PM2.5 induced lung oxidative stress injury and protective effect of lipoic acid against the injury in rats[J]. Chinese Journal of Public Health, 2018, 34(12): 1646-1649. DOI: 10.11847/zgggws1119847

PM2.5致大鼠肺氧化应激损伤及硫辛酸保护作用

PM2.5 induced lung oxidative stress injury and protective effect of lipoic acid against the injury in rats

  • 摘要:
      目的  探讨PM2.5对大鼠肺氧化应激损伤及不同剂量硫辛酸(ALA)的保护作用。
      方法  SPF级雄性SD大鼠48只随机分为对照组、PM2.5组、低、中、高剂量硫辛酸组。不同剂量硫辛酸预处理大鼠24 h后,气管滴注PM2.5连续3 d,禁食8 h后处死,取肺泡灌洗液及肺组织,试剂盒法检测超氧化物歧化酶(SOD)、谷胱甘肽(GSH)、谷胱甘肽过氧化物酶(GSH-Px)和丙二醛(MDA)等指标。
      结果  与对照组比较,PM2.5组大鼠体重增重(63.5 ± 3.69)g下降;与PM2.5组比较,高剂量硫辛酸组大鼠体重增重(93.56 ± 4.31)g明显增加。与对照组比较,PM2.5组大鼠血清SOD、GSH水平显著降低(P < 0.05);与PM2.5组比较,中、高剂量硫辛酸组大鼠血清SOD、GSH-Px、GSH水平升高,差异有统计学意义(P < 0.05)。与对照组比较,PM2.5组大鼠肺泡灌洗液中GSH-Px、GSH水平显著降低,MDA含量、GSSG/GSH比值增加(P < 0.05);与PM2.5组比较,中、高剂量硫辛酸组大鼠肺泡灌洗液中GSH-Px、GSH升高,GSSG/GSH比值降低(P < 0.05)。与对照组比较,PM2.5组大鼠肺组织中SOD、GSH-Px、GSH水平显著降低,MDA含量、GSSG/GSH比值增加(P < 0.05);与PM2.5组比较,高剂量硫辛酸组大鼠肺组织中SOD、GSH水平升高,GSSG/GSH比值明显降低(P < 0.05)。
      结论  一定剂量PM2.5可导致大鼠肺氧化损伤,硫辛酸对PM2.5导致的肺氧化损伤具有一定程度的保护作用。

     

    Abstract:
      Objective  To observe lung oxidative stress injury induced by particulate matter ≤ 2.5 μm in aerodynamic diameter (PM2.5) and the effect of different dose alpha lipoic acid (ALA) against the injury in rats.
      Methods  Totally 48 male specific pathogen free Sprague-Dawley rats were randomly assigned into a PM2.5 group with intratracheal instillation of suspension (2 ml/kg) of PM2.5 sampled from ambient air in Weifang city once a day for three days, and three groups of PM2.5 plus low, moderate and high dose ALA (intraperitoneal injection at dosages of 20, 40, 80 μg/kg 24 hours before the PM2.5 treatment), and a control group with intratracheal instillation and intraperitoneal injection of saline. By the end of the treatments, all the rats were sacrificed after 8 hours of fasting; then, bronchoalveolar lavage fluid (BALF) and lung tissue specimens were collected for detections of superoxide dismutase (SOD), glutathione (GSH), glutathione peroxidase (GSH-Px), and malondialdehyde (MDA) using kit assays.
      Results  The body weight gain of PM2.5 group was significantly lower than that of control group (63.5 ± 3.69 g vs. 96.35 ± 4.32 g); while the body weight gain (93.56 ± 4.31 g) of PM2.5 plus high-dose ALA pretreatment group was significantly higher than that of PM2.5 group. Compared to those of the control group, the serum SOD and GSH of PM2.5 group decreased significantly (both P < 0.05) and compared to those of the PM2.5 group, the serum SOD, GSH-Px, and GSH of the PM2.5 plus moderate and high ALA pretreatment group increased significantly (P < 0.05 for all). The GSH-Px and GSH decreased significantly but the MDA and glutathione disulfide (GSSG)/GSH ratio increased significantly in BALF of the PM2.5 group in comparison to those of the control group (P < 0.05 for all); while, the GSH-Px and GSH increased but the GSSG/GSH ratio in BALF of the PM2.5 plus moderate and high ALA pretreatment group decreased significantly in contrast to those of the PM2.5 group (P < 0.05 for all). Significantly decreased SOD, GSH-Px, and GSH and increased MDA and GSSG/GSH ratio were observed in lung tissues of the PM2.5 group compared to those of the control group (P < 0.05 for all); whereas, the PM2.5 plus high ALA pretreatment group demonstrated significantly increased SOD and GSH and decreased GSSG/GSH ratio compared to the PM2.5 group (P < 0.05 for all).
      Conclusion  PM2.5 at certain dosages could induce lung oxidative damage and pretreatment with different dose of alpha lipoic acid is of protective effect against the injury in rats.

     

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