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暴露于高氧环境并经气管内给予聚乙二醇过氧化氢酶和超氧化物歧化酶处理的幼鼠的肺抗氧化酶及心肺反应

Lung antioxidant enzymes and cardiopulmonary responses in young rats exposed to hyperoxia and treated intratracheally with PEG catalase and superoxide dismutase.

作者信息

Thibeault D W, Rezaiekhaligh M, Mabry S

机构信息

University of Missouri-Kansas City School of Medicine, Children's Mercy Hospital 64108-9898.

出版信息

Exp Lung Res. 1993 Mar-Apr;19(2):137-51. doi: 10.3109/01902149309031716.

Abstract

The 27-day-old rat exposed to 100% oxygen (O2) for 8 days will have predictable lung vascular and parenchymal changes at 60 days of age. Using this model, the goals of this study are (1) to measure the lung antioxidant enzyme activities serially following intratracheal PEG antioxidant therapy during the 8-day O2 exposure; and (2) to assess chronic cardiopulmonary changes in the O2-exposed rats treated with PEG-CAT and/or PEG-CuZn SOD given intraperitoneally (IP) and/or intratracheally (IT). The study encompassed 202 male rats exposed to room air or oxygen. CuZn SOD doses were 300 U IT and 2000 U IP. The CAT dose was 500 or 4000 U IT and 10,000 U IP. At 60 days of age, the right ventricular systolic pressure (RVP), RV weight, % acinar wall arterial thickness, and parenchymal air space were significantly increased in O2-exposed rats compared to RA rats. The RVP, RV weight, and parenchymal changes were prevented by daily IT PEG-CAT 4000 U + CuZn SOD 300 U but the increased small artery muscularization was not. Three hours after the initial dose of IT PEG-CAT 4000 U, lung CAT activity was more than doubled and remained constant throughout the 8-day daily treatment course. This dose of CAT depressed the induction response to O2 of CuZn and MnSOD. It is concluded that daily intratracheal administration of PEG-CAT 4000 U + CuZn SOD 300 U can significantly ameliorate some of the chronic parenchymal and vascular lung O2 toxic changes. However, it appears that high-dose exogenous PEG-CAT suppresses the endogenous enzyme induction to hyperoxia of both CuZn and Mn-SOD.

摘要

27日龄的大鼠暴露于100%氧气(O₂)8天,在60日龄时会出现可预测的肺血管和实质变化。利用该模型,本研究的目标是:(1)在8天的氧气暴露期间,连续测量气管内给予聚乙二醇(PEG)抗氧化剂治疗后肺抗氧化酶活性;(2)评估经腹腔内(IP)和/或气管内(IT)给予聚乙二醇 - 过氧化氢酶(PEG - CAT)和/或聚乙二醇 - 铜锌超氧化物歧化酶(PEG - CuZn SOD)治疗的氧气暴露大鼠的慢性心肺变化。该研究纳入了202只暴露于室内空气或氧气的雄性大鼠。铜锌超氧化物歧化酶的剂量为气管内300 U和腹腔内2000 U。过氧化氢酶的剂量为气管内500或4000 U和腹腔内10,000 U。在60日龄时,与暴露于室内空气的大鼠相比,氧气暴露大鼠的右心室收缩压(RVP)、右心室重量、腺泡壁动脉厚度百分比和实质气腔显著增加。每日气管内给予4000 U聚乙二醇-过氧化氢酶+ 300 U铜锌超氧化物歧化酶可预防右心室收缩压、右心室重量和实质变化,但小动脉肌化增加未得到预防。在首次给予4000 U气管内聚乙二醇-过氧化氢酶3小时后,肺过氧化氢酶活性增加了一倍多,并在8天的每日治疗过程中保持恒定。该剂量的过氧化氢酶抑制了铜锌和锰超氧化物歧化酶对氧气的诱导反应。结论是,每日气管内给予4000 U聚乙二醇-过氧化氢酶+ 300 U铜锌超氧化物歧化酶可显著改善一些慢性肺实质和血管性氧气毒性变化。然而,高剂量外源性聚乙二醇-过氧化氢酶似乎抑制了铜锌和锰超氧化物歧化酶对高氧的内源性酶诱导。

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