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狒狒模型中致死性低血压菌血症时接触系统的激活

Activation of the contact system in lethal hypotensive bacteremia in a baboon model.

作者信息

Pixley R A, DeLa Cadena R A, Page J D, Kaufman N, Wyshock E G, Colman R W, Chang A, Taylor F B

机构信息

Thrombosis Research Center, Temple University School of Medicine, Philadelphia, Pennsylvania 19140.

出版信息

Am J Pathol. 1992 Apr;140(4):897-906.

Abstract

The hypotension in septicemia is believed to be mediated by the combined action of many mediators including cytokines, prostaglandins, and complement components. To evaluate the contribution of the contact/kinin-forming system to hypotension, the authors used an established experimental baboon model of bacteremia in which two concentrations of Escherichia Coli (E. coli) were used to produce lethal and nonlethal hypotension. The lethal group (n = 5) developed irreversible hypotension that significantly correlated with the decline in levels of high molecular weight kininogen (HK) and an increase in alpha 2 macroglobulin-kallikrein complexes (alpha 2M-kal). The nonlethal group (n = 9) experienced reversible hypotension, a less striking decline in HK, and only slight elevation in alpha 2M-kal. No significant changes were found in levels of factor XII, prekallikrein, and factor XI in either group. A significant change in the contact system, which reflects the fatal outcome, is the rise in alpha 2M-kal. This study suggests that irreversible hypotension correlates with prolonged activation of the contact system.

摘要

败血症中的低血压被认为是由多种介质共同作用介导的,这些介质包括细胞因子、前列腺素和补体成分。为了评估接触/激肽形成系统对低血压的作用,作者使用了一种已建立的狒狒菌血症实验模型,其中使用两种浓度的大肠杆菌(E. coli)来产生致死性和非致死性低血压。致死组(n = 5)出现不可逆性低血压,这与高分子量激肽原(HK)水平下降以及α2巨球蛋白-激肽释放酶复合物(α2M-kal)增加显著相关。非致死组(n = 9)经历可逆性低血压,HK下降不太明显,α2M-kal仅略有升高。两组中因子 XII、前激肽释放酶和因子 XI 的水平均未发现显著变化。反映致命结局的接触系统的一个显著变化是α2M-kal的升高。这项研究表明,不可逆性低血压与接触系统的长期激活相关。

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