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Role of granulocyte elastase in tissue injury in patients with septic shock complicated by multiple-organ failure.

机译:败血性休克并发多器官衰竭的患者中粒细胞弹性蛋白酶在组织损伤中的作用。

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摘要

To better understand the role of granulocyte elastase (GE) in mediating tissue injury during sepsis, GE levels were measured in plasma and bronchoalveolar lavage fluid (BALF) in patients with septic shock (n = 16) and hemorrhagic shock (n = 30). Granulocyte elastase levels were compared to levels of alpha 1-protease inhibitor (alpha 1-PI). Results show that although plasma GE-alpha 1-PI complex was initially elevated in patients with hemorrhagic and septic shock, elevations in plasma GE-alpha 1-PI complex (831 +/- 241 micrograms/L) persisted in septic shock patients. alpha 1-Protease inhibitor levels in serum were increased, resulting in an inhibition of serum GE activity. Granulocyte elastase activity in BALF, however, was significantly higher in those patients with septic, as compared to hemorrhagic shock (31.4 +/- 25.8 versus 3.7 +/- 4.0 U/L, respectively). In addition GE levels were compared to other parameters, including respiratory index, blood neutrophil count, and plasma levels of endotoxin, fibronectin, and coagulation factor XIII. Significant correlations were observed between GE-alpha 1-PI and increased endotoxin concentration and decreased fibronectin and coagulation factor XIII levels. Significant correlation was found also between GE activity in BALF and respiratory index. These findings suggest that severe tissue damage occurred in patients with septic shock complicated by multiple-organ failure. Although GE activity appeared to be adequately inhibited by alpha 1-PI in blood, increased GE activity in local tissues, such as lung alveoli, may be responsible for significant local tissue injury during septic shock.
机译:为了更好地了解粒细胞弹性蛋白酶(GE)在败血症过程中介导的组织损伤中的作用,对败血性休克(n = 16)和失血性休克(n = 30)患者的血浆和支气管肺泡灌洗液(BALF)中的GE水平进行了测量。将粒细胞弹性蛋白酶水平与α1-蛋白酶抑制剂(α1-P​​I)水平进行比较。结果表明,尽管出血性和败血性休克患者血浆GE-alpha 1-PI复合物最初升高,但脓毒症休克患者血浆GE-alpha 1-PI复合物持续升高(831 +/- 241微克/升)。血清中的α1-蛋白酶抑制剂水平增加,导致血清GE活性受到抑制。然而,败血性休克患者中BALF中的粒细胞弹性蛋白酶活性显着高于失血性休克(分别为31.4 +/- 25.8和3.7 +/- 4.0 U / L)。此外,将GE水平与其他参数进行了比较,包括呼吸指数,血液中性粒细胞计数以及内毒素,纤连蛋白和凝血因子XIII的血浆水平。 GE-alpha 1-PI与内毒素浓度增加,纤连蛋白和凝血因子XIII水平降低之间存在显着相关性。在BALF中的GE活性与呼吸指数之间也发现了显着相关性。这些发现表明,败血性休克并发多器官衰竭的患者发生了严重的组织损伤。尽管GE活性似乎被血液中的α1-PI充分抑制,但是在脓毒性休克期间局部组织(例如肺泡)中GE活性的增加可能是造成局部组织严重损伤的原因。

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