Ultrafast Cooling With Total Liquid Ventilation Mitigates Early Inflammatory Response and Offers Neuroprotection in a Porcine Model of Cardiac Arrest

• Published in: Journal of the American Heart Association Vol. 13; no. 16; p. e035617
• Main Authors: Abi Zeid Daou, Yara, Watanabe, Naoto, Lidouren, Fanny, Bois, Antoine, Faucher, Estelle, Huet, Hélène, Hutin, Alice, Jendoubi, Ali, Surenaud, Mathieu, Hue, Sophie, Nadeau, Mathieu, Perrotto, Sandrine, Libardi, Mickaël, Ghaleh, Bijan, Micheau, Philippe, Bruneval, Patrick, Cariou, Alain, Kohlhauer, Matthias, Tissier, Renaud
• Format: Journal Article
• Language: English
• Published: England Wiley-Blackwell 20.08.2024; Wiley
• Subjects: Animals; Brain - metabolism; Brain - pathology; cardiac arrest; Cardiopulmonary Resuscitation - methods; Cytokines - blood; Cytokines - metabolism; Disease Models, Animal; Heart Arrest - therapy; hypothermia; Hypothermia, Induced - methods; inflammation; Inflammation Mediators - blood; Inflammation Mediators - metabolism; Life Sciences; liquid ventilation; Liquid Ventilation - methods; Neuroprotection; Swine; Time Factors; hypothermia; inflammation; cardiac arrest; liquid ventilation; Liquid ventilation; Inflammation; Cardiac arrest; Hypothermia
• ISSN: 2047-9980; 2047-9980
• DOI: 10.1161/JAHA.124.035617

Brain injury is one of the most serious complications after cardiac arrest (CA). To prevent this phenomenon, rapid cooling with total liquid ventilation (TLV) has been proposed in small animal models of CA (rabbits and piglets). Here, we aimed to determine whether hypothermic TLV can also offer neuroprotection and mitigate cerebral inflammatory response in large animals. Anesthetized pigs were subjected to 14 minutes of ventricular fibrillation followed by cardiopulmonary resuscitation. After return of spontaneous circulation, animals were randomly subjected to normothermia (control group, n=8) or ultrafast cooling with TLV (TLV group, n=8). In the latter group, TLV was initiated within a window of 15 minutes after return of spontaneous circulation and allowed to reduce tympanic, esophageal, and bladder temperature to the 32 to 34 °C range within 30 minutes. After 45 minutes of TLV, gas ventilation was resumed, and hypothermia was maintained externally until 3 hours after CA, before rewarming using heat pads (0.5 °C-1 °C/h). After an additional period of progressive rewarming for 3 hours, animals were euthanized for brain withdrawal and histological analysis. At the end of the follow-up (ie, 6 hours after CA), histology showed reduced brain injury as witnessed by the reduced number of Fluroro-Jade C-positive cerebral degenerating neurons in TLV versus control. IL (interleukin)-1ra and IL-8 levels were also significantly reduced in the cerebrospinal fluid in TLV versus control along with cerebral infiltration by CD3+ cells. Conversely, circulating levels of cytokines were not different among groups, suggesting a discrepancy between local and systemic inflammatory levels. Ultrafast cooling with TLV mitigates neuroinflammation and attenuates acute brain lesions in the early phase following resuscitation in large animals subjected to CA.