Johnson D A, Winters R S, Lee K R, Smith C E
Department of Biochemistry, James H. Quillen College of Medicine, East Tennessee State University, Johnson City 37614-0002.
Res Rep Health Eff Inst. 1990 Dec(37):1-39.
This project tested the hypothesis that inhaled oxidants could cause lung damage by inactivating the proteinase inhibitors that normally protect the lung from proteolysis. Rat alpha-1-proteinase inhibitor (alpha 1-PI)2 was purified from blood plasma, and antibodies to this inhibitor were prepared. The activity of alpha 1-PI in lung lavage fluids from rats was measured by elastase inhibition, and the immunological concentration of alpha 1-PI was quantified in an enzyme-linked immunoassay. The ratio of the amount of active alpha 1-PI relative to its immunological concentration was examined as a measure of the inhibitor's functional activity. This ratio and the ratio of the immunological concentration of alpha 1-PI to the total protein concentration were determined in lung lavage fluids from rats exposed to air, 10 parts per million (ppm) nitrogen dioxide, and diesel emissions (3.5 mg/m3 particulates) for 12, 18, and 24 months. Only diesel exposures resulted in a statistically significant reduction in the functional activity of alpha 1-PI of 30 percent (p less than 0.05). Similar studies were performed on rats exposed to nitrogen dioxide (0.5 ppm background with peaks of 1.5 ppm) and ozone (0.06 ppm background with peaks of 0.25 ppm) for 12 and 18 months. No statistically significant effects were observed in the functional activity of alpha 1-PI or its immunological concentration. In other protocols, rats were acutely exposed to 0.8 ppm or 1.2 ppm ozone for two, four, or eight hours, and to 0.5 ppm or 0.8 ppm ozone in conjunction with 8 percent carbon dioxide for two or seven hours. Although these acute exposure conditions did not reduce the functional activity of alpha 1-PI, the immunological concentration of alpha 1-PI and the elastase inhibitory activity, relative to other proteins, were significantly increased in relation to the total amount of ozone inhaled. The functional activity of alpha 1-PI also was measured in the bronchoalveolar lavage fluids of human subjects exposed to nitrogen dioxide (0.05 ppm with 2 ppm peaks, or to 1.5 ppm continuously) for three hours and to ozone (0.4 ppm) for two hours during exercise. These exposures did not result in significant changes in the functional activity of alpha 1-PI or its immunological concentration.(ABSTRACT TRUNCATED AT 400 WORDS)
吸入性氧化剂可通过使正常情况下保护肺部免受蛋白水解的蛋白酶抑制剂失活,从而导致肺损伤。从大鼠血浆中纯化出大鼠α-1-蛋白酶抑制剂(α1-PI),并制备了针对该抑制剂的抗体。通过弹性蛋白酶抑制法测定大鼠肺灌洗液中α1-PI的活性,并在酶联免疫分析中对α1-PI的免疫浓度进行定量。检测活性α1-PI的量与其免疫浓度的比值,作为抑制剂功能活性的指标。在暴露于空气、百万分之十(ppm)二氧化氮和柴油废气(3.5毫克/立方米颗粒物)12、18和24个月的大鼠肺灌洗液中,测定该比值以及α1-PI免疫浓度与总蛋白浓度的比值。只有柴油暴露导致α1-PI的功能活性在统计学上显著降低30%(p小于0.05)。对暴露于二氧化氮(背景浓度0.5 ppm,峰值浓度1.5 ppm)和臭氧(背景浓度0.06 ppm,峰值浓度0.25 ppm)12和18个月的大鼠进行了类似研究。未观察到α1-PI的功能活性或其免疫浓度有统计学上的显著影响。在其他实验方案中,大鼠急性暴露于0.8 ppm或1.2 ppm的臭氧中2、4或8小时,以及暴露于0.5 ppm或0.8 ppm的臭氧与8%二氧化碳的混合气体中2或7小时。尽管这些急性暴露条件并未降低α1-PI的功能活性,但相对于吸入臭氧的总量,α1-PI的免疫浓度和弹性蛋白酶抑制活性相对于其他蛋白质显著增加。还在运动期间暴露于二氧化氮(0.05 ppm,峰值浓度2 ppm,或持续暴露于1.5 ppm)3小时和臭氧(0.4 ppm)2小时的人类受试者的支气管肺泡灌洗液中测量了α1-PI的功能活性。这些暴露并未导致α1-PI的功能活性或其免疫浓度发生显著变化。(摘要截选至400字)