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雾化吸入的中性内肽酶可逆转臭氧诱导的气道对P物质的高反应性。

Aerosolized neutral endopeptidase reverses ozone-induced airway hyperreactivity to substance P.

作者信息

Murlas C G, Lang Z, Williams G J, Chodimella V

机构信息

Department of Medicine, Rush University, Chicago, Illinois 60612.

出版信息

J Appl Physiol (1985). 1992 Mar;72(3):1133-41. doi: 10.1152/jappl.1992.72.3.1133.

Abstract

We investigated the effects of ozone exposure (3.0 ppm, 2 h) on airway neutral endopeptidase (NEP) activity and bronchial reactivity to substance P in guinea pigs. Reactivity after ozone or air exposure was determined by measuring specific airway resistance in intact unanesthetized spontaneously breathing animals in response to increasing doses of intravenous substance P boluses. The effective dose of substance P (in micrograms) that produced a doubling of baseline specific airway resistance (ED200SP) was determined by interpolation of cumulative substance P dose-response curves. NEP activity was measured in tracheal homogenates made from each animal of other groups exposed to either ozone or room air. By reverse-phase high-pressure liquid chromatography, this activity was characterized by the phosphoramidon-inhibitable cleavage of alanine-p-nitroaniline from succinyl-(Ala)3-p-nitroaniline in the presence of 100 microM amastatin. Mean values of the changes in log ED200SP were 0.27 +/- 0.07 (SE) for the ozone-exposed group and 0.08 +/- 0.04 for the air-exposed group. We found that phosphoramidon significantly increased substance P reactivity in the air-exposed animals (P less than 0.01), but it had no effect in the ozone-exposed group. This finding was associated with a significant reduction in tracheal homogenate NEP activity of ozone-exposed animals compared with controls: mean values were 18.1 +/- 1.9 nmol.min-1.mg protein-1 for the ozone-exposed group and 25.1 +/- 2.4 nmol.min-1.mg protein-1 for air-exposed animals (P less than 0.05). Inhalation of an aerosolized NEP preparation, partially purified from guinea pig kidney, reversed the substance P hyperreactivity produced by ozone exposure.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们研究了臭氧暴露(3.0 ppm,2小时)对豚鼠气道中性内肽酶(NEP)活性以及支气管对P物质反应性的影响。通过测量完整、未麻醉、自主呼吸动物静脉注射递增剂量P物质推注后特定气道阻力,来确定臭氧或空气暴露后的反应性。通过对累积P物质剂量 - 反应曲线进行插值,确定使基线特定气道阻力加倍的P物质有效剂量(以微克计,ED200SP)。在暴露于臭氧或室内空气的其他组的每只动物的气管匀浆中测量NEP活性。通过反相高压液相色谱法,在100 microM抑氨肽酶存在的情况下,该活性以磷酰胺脒可抑制的琥珀酰 - (丙氨酸)3 - 对硝基苯胺中丙氨酸 - 对硝基苯胺的裂解为特征。臭氧暴露组log ED200SP变化的平均值为0.27±0.07(SE),空气暴露组为0.08±0.04。我们发现磷酰胺脒显著增加了空气暴露动物对P物质的反应性(P <0.01),但对臭氧暴露组没有影响。这一发现与臭氧暴露动物的气管匀浆NEP活性与对照组相比显著降低有关:臭氧暴露组的平均值为18.1±1.9 nmol·min-1·mg蛋白-1,空气暴露动物为25.1±2.4 nmol·min-1·mg蛋白-1(P <0.05)。吸入从豚鼠肾脏部分纯化的雾化NEP制剂,可逆转臭氧暴露引起的P物质高反应性。(摘要截短于250字)

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