4.6 Article

Ultrafast Hypothermia Selectively Mitigates the Early Humoral Response After Cardiac Arrest

期刊

出版社

WILEY
DOI: 10.1161/JAHA.120.017413

关键词

critical care; liquid ventilation; therapeutic hypothermia

资金

  1. Agence Nationale pour la Recherche (COOLIVENT Grant)

向作者/读者索取更多资源

BACKGROUND: Total liquid ventilation (TLV) has been shown to prevent neurological damage though ultrafast cooling in animal models of cardiac arrest. We investigated whether its neuroprotective effect could be explained by mitigation of early inflammatory events. Methods and Results: Rabbits were submitted to 10 minutes of ventricular fibrillation. After resuscitation, they underwent normothermic follow-up (control) or ultrafast cooling by TLV and hypothermia maintenance for 3 hours (TLV). Immune response, survival, and neurological dysfunction were assessed for 3 days. TLV improved neurological recovery and reduced cerebral lesions and leukocyte infiltration as compared with control (eg, neurological dysfunction score=34 +/- 6 versus 66 +/- 6% at day 1, respectively). TLV also significantly reduced interleukin-6 blood levels during the hypothermic episode (298 +/- 303 versus 991 +/- 471 pg/mL in TLV versus control at 3 hours after resuscitation, respectively), but not after rewarming (752 +/- 563 versus 741 +/- 219 pg/mL in TLV versus control at 6 hours after resuscitation, respectively). In vitro assays confirmed the high temperature sensitivity of interleukin-6 secretion. Conversely, TLV did not modify circulating high-mobility group box 1 levels or immune cell recruitment into the peripheral circulation. The link between interleukin-6 early transcripts (<8 hours) and neurological outcome in a subpopulation of the previously described Epo-ACR-02 (High Dose of Erythropoietin Analogue After Cardiac Arrest) trial confirmed the importance of this cytokine at the early stages as compared with delayed stages (>8 hours). Conclusions: The neuroprotective effect of hypothermic TLV was associated with a mitigation of humoral interleukin-6 response. A temperature-dependent attenuation of immune cell reactivity during the early phase of the post-cardiac arrest syndrome could explain the potent effect of rapid hypothermia. REGISTRATION: URL: https://www.clinicaltrials.gov; Unique identifier: NCT00999583.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据