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过氧化物酶体增殖物激活受体6基因靶向小鼠在百草枯诱导的氧化应激下肺损伤增加。

Peroxiredoxin 6 gene-targeted mice show increased lung injury with paraquat-induced oxidative stress.

作者信息

Wang Yan, Feinstein Sheldon I, Manevich Yefim, Ho Ye-Shih, Fisher Aron B

机构信息

Institute for Environmental Medicine, University of Pennsylvania Medical Center, Philadelphia, Pennsylvania 19104-6068, USA.

出版信息

Antioxid Redox Signal. 2006 Jan-Feb;8(1-2):229-37. doi: 10.1089/ars.2006.8.229.

Abstract

Mice with knock-out of peroxiredoxin 6 (Prdx6), a recently described antioxidant enzyme, were evaluated for susceptibility to lung injury with paraquat (PQ) administration. With high dose PQ (30 mg/kg i.p.), all Prdx6-/- mice died (LT50 54 +/- 2.05 h, mean +/- SE) by 4 days, whereas 86% of the wild-type (WT) mice (C57BL/6) survived (n = 14). At 2 days after PQ, lung wet/dry weight ratio increased significantly (p < 0.05) to 7.57 +/- 0.37 in Prdx6-/- mice vs. 5.42 +/- 0.25 in WT mice. Total protein and nucleated cells in bronchoalveolar lavage fluid and TBARS and protein carbonyls in lung homogenate also showed more marked increases in Prdx6-/- mice. At 2.5 days after PQ, light microscopy of WT lungs showed mild injury while Prdx6-/- lungs showed epithelial cell necrosis, perivascular edema, and inflammatory cells. With low dose PQ (12.5 mg/kg), mortality and lung injury were less marked but were significantly greater with Prdx6-/- compared to WT mice. These results show that Prdx6-/- mice have increased susceptibility to lung injury with PQ administration. Thus, Prdx6 protects lungs against PQ toxicity as shown previously for hyperoxia, indicating that it functions as an important lung antioxidant enzyme.

摘要

对敲除最近发现的抗氧化酶过氧化物酶6(Prdx6)的小鼠进行百草枯(PQ)给药,评估其对肺损伤的易感性。给予高剂量PQ(30 mg/kg腹腔注射)后,所有Prdx6基因敲除小鼠在4天内死亡(半数致死时间54±2.05小时,平均值±标准误),而86%的野生型(WT)小鼠(C57BL/6)存活(n = 14)。PQ给药2天后,Prdx6基因敲除小鼠的肺湿/干重比显著增加(p < 0.05),达到7.57±0.37,而WT小鼠为5.42±0.25。支气管肺泡灌洗液中的总蛋白和有核细胞以及肺匀浆中的硫代巴比妥酸反应物(TBARS)和蛋白质羰基也显示Prdx6基因敲除小鼠的增加更为明显。PQ给药2.5天后,WT小鼠肺的光学显微镜检查显示轻度损伤,而Prdx6基因敲除小鼠的肺显示上皮细胞坏死、血管周围水肿和炎症细胞。给予低剂量PQ(12.5 mg/kg)时,死亡率和肺损伤不太明显,但Prdx6基因敲除小鼠比WT小鼠明显更严重。这些结果表明,Prdx6基因敲除小鼠对PQ给药引起的肺损伤易感性增加。因此,如先前在高氧环境中所显示的,Prdx6可保护肺免受PQ毒性,表明它作为一种重要的肺抗氧化酶发挥作用。

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