Mortaza Satar, Martinez M Carmen, Baron-Menguy Céline, Burban Mélanie, de la Bourdonnaye Mathilde, Fizanne Lionel, Pierrot Marc, Calès Paul, Henrion Daniel, Andriantsitohaina Ramaroson, Mercat Alain, Asfar Pierre, Meziani Ferhat
Laboratoire HIFIH UPRES EA 3859 , Université d'Angers, Angers, France.
Crit Care Med. 2009 Jun;37(6):2045-50. doi: 10.1097/CCM.0b013e3181a00629.
Microparticles (MPs) are membrane vesicles with procoagulant and proinflammatory properties released during cell activation and might be potentially involved in the pathophysiology of septic shock. This study was designed to assess the effects of MPs from septic origin on the systemic hemodynamics as well as on the inflammatory, oxidative, and nitrosative stresses.
A prospective, randomized, controlled experimental study with repeated measurements.
Investigational animal laboratory.
Forty healthy rats were randomly allocated to three groups: 10 animals inoculated with MPs isolated from control rats (cMPs), 15 animals inoculated with MPs isolated from sham rats (shMPs), and 15 animals inoculated with MPs isolated from rats with peritonitis (sMPs).
Rats were anesthetized, mechanically ventilated, and infused with the same amount of cMPs, shMPs, or sMPs. We measured the heart rate, mean arterial pressure, carotid artery, and portal vein blood flows. Hemodynamic parameters were recorded during 7 hours, and then animals were killed. Aorta and heart were harvested for further in vitro tissue analyses.
Rats with sepsis induced by peritonitis exhibited a specific phenotype of MPs. Inoculation of sMPs in healthy rats reproduced hemodynamic, septic inflammatory patterns, associated with oxidative and nitrosative stresses.
微粒(MPs)是细胞活化过程中释放的具有促凝和促炎特性的膜泡,可能参与脓毒性休克的病理生理过程。本研究旨在评估源自脓毒症的微粒对全身血流动力学以及炎症、氧化和亚硝化应激的影响。
一项重复测量的前瞻性、随机、对照实验研究。
实验动物实验室。
40只健康大鼠随机分为三组:10只接种从对照大鼠分离的微粒(cMPs),15只接种从假手术大鼠分离的微粒(shMPs),15只接种从腹膜炎大鼠分离的微粒(sMPs)。
大鼠麻醉后进行机械通气,并输注等量的cMPs、shMPs或sMPs。我们测量心率、平均动脉压、颈动脉和门静脉血流量。在7小时内记录血流动力学参数,然后处死动物。采集主动脉和心脏进行进一步的体外组织分析。
1)脓毒症大鼠微粒的细胞来源(表型)而非循环浓度不同,其特征是白细胞来源的微粒显著增加。2)sMPs而非cMPs或shMPs降低了平均动脉压,对颈动脉和门静脉血流量无影响。3)接种sMPs的大鼠超氧阴离子生成增加、核因子κB活性增加、诱导型一氧化氮合酶过度表达,随后一氧化氮过度生成,内皮型一氧化氮合酶活化降低。
腹膜炎诱导的脓毒症大鼠表现出特定的微粒表型。在健康大鼠中接种sMPs可重现与氧化和亚硝化应激相关的血流动力学、脓毒症炎症模式。