Dwenger A, Schweitzer G, Regel G
J Clin Chem Clin Biochem. 1986 Jan;24(1):73-88. doi: 10.1515/cclm.1986.24.1.73.
The technique of bronchoalveolar lavage was used to obtain serial samples of lavage every two days from non-contused lung areas of seven traumatized patients and four normals; blood was drawn simultaneously. Urea, total protein, albumin, alpha 1-proteinase inhibitor, alpha 2-macroglobulin, lactate dehydrogenase, beta-N-acetyl-glucosaminidase, myeloperoxidase, and elastase enzyme activity, as well as complexed and total elastase concentrations were determined in bronchoalveolar lavage fluids and plasma samples. Lavage fluid cell pattern was counted. Polymorphonuclear leukocytes were isolated from lavage fluids and blood samples. Granulocyte contents of elastase enzyme activity, complexed and total elastase concentrations, and myeloperoxidase and lactate dehydrogenase activity were determined. Polymorphonuclear leukocyte stimulatory functions were measured by luminol-enhanced chemiluminescence. The following results were obtained for the patient group: Patterns of lavage fluid cells were shifted in favour of polymorphonuclear leukocytes and lymphocytes. The protein determinations of bronchoalveolar lavage fluids and plasma samples gave information about the extent of alterations of permeability of the capillary-interstitial-alveolar space (albumin/urea and alpha 1-proteinase inhibitor/urea ratios) as well as about the amounts of cytoplasmic and lysosomal enzymes released by phagocytes (lactate dehydrogenase/urea, beta-N-acetylglucosaminidase/urea, elastase/urea ratios). Polymorphonuclear leukocytes isolated from bronchoalveolar lavage fluids contained a decreased content of myeloperoxidase and elastase enzyme activities and total elastase concentration; the content of complexed elastase was found to be increased more than 100 fold. From chemiluminescence measurements there was evidence for decreased zymosan-induced stimulatory function, while the photon emission rate of polymorphonuclear leukocytes after passage into the alveolar space was increased.
采用支气管肺泡灌洗技术,每两天从7名创伤患者和4名正常人未受挫伤的肺区域获取系列灌洗样本;同时采集血液。测定支气管肺泡灌洗液和血浆样本中的尿素、总蛋白、白蛋白、α1-蛋白酶抑制剂、α2-巨球蛋白、乳酸脱氢酶、β-N-乙酰氨基葡萄糖苷酶、髓过氧化物酶和弹性蛋白酶活性,以及结合型和总弹性蛋白酶浓度。对灌洗液细胞模式进行计数。从灌洗液和血液样本中分离出多形核白细胞。测定粒细胞中弹性蛋白酶活性、结合型和总弹性蛋白酶浓度以及髓过氧化物酶和乳酸脱氢酶活性。通过鲁米诺增强化学发光法测定多形核白细胞的刺激功能。患者组获得以下结果:灌洗液细胞模式向多形核白细胞和淋巴细胞偏移。支气管肺泡灌洗液和血浆样本的蛋白质测定提供了有关毛细血管-间质-肺泡空间通透性改变程度(白蛋白/尿素和α1-蛋白酶抑制剂/尿素比值)以及吞噬细胞释放的细胞质和溶酶体酶量(乳酸脱氢酶/尿素、β-N-乙酰氨基葡萄糖苷酶/尿素、弹性蛋白酶/尿素比值)的信息。从支气管肺泡灌洗液中分离出的多形核白细胞中髓过氧化物酶和弹性蛋白酶活性以及总弹性蛋白酶浓度降低;发现结合型弹性蛋白酶含量增加超过100倍。化学发光测量结果表明,酵母聚糖诱导的刺激功能降低,而多形核白细胞进入肺泡空间后的光子发射率增加。