Analysis of cerebral Interleukin-6 and tumor necrosis factor alpha patterns following different ventilation strategies during cardiac arrest in pigs
- PMID: 37790622
- PMCID: PMC10544304
- DOI: 10.7717/peerj.16062
Analysis of cerebral Interleukin-6 and tumor necrosis factor alpha patterns following different ventilation strategies during cardiac arrest in pigs
Abstract
Hypoxia-induced neuroinflammation after cardiac arrest has been shown to be mitigated by different ventilation methods. In this prospective randomized animal trial, 35 landrace pigs were randomly divided into four groups: intermittent positive pressure ventilation (IPPV), synchronized ventilation 20 mbar (SV 20 mbar), chest compression synchronized ventilation 40 mbar (CCSV 40 mbar) and a control group (Sham). After inducing ventricular fibrillation, basic life support (BLS) and advanced life support (ALS) were performed, followed by post-resuscitation monitoring. After 6 hours, the animals were euthanized, and direct postmortem brain tissue samples were taken from the hippocampus (HC) and cortex (Cor) for molecular biological investigation of cytokine mRNA levels of Interleukin-6 (IL-6) and tumor necrosis factor alpha (TNFα). The data analysis showed that CCSV 40 mbar displayed low TNFα mRNA-levels, especially in the HC, while the highest TNFα mRNA-levels were detected in SV 20 mbar. The results indicate that chest compression synchronized ventilation may have a potential positive impact on the cytokine expression levels post-resuscitation. Further studies are needed to derive potential therapeutic algorithms from these findings.
Keywords: Chest-compressions; Interleukines; Neuroinflammation; Porcine; Resuscitation; Synchronized-ventilation.
©2023 Renz et al.
Conflict of interest statement
The synchronized ventilation devices were provided by Weinmann Medical unconditionally and for research purposes only. The authors declare there are no competing interests.
Figures



Similar articles
-
Chest Compression Synchronized Ventilation versus Intermitted Positive Pressure Ventilation during Cardiopulmonary Resuscitation in a Pig Model.PLoS One. 2015 May 26;10(5):e0127759. doi: 10.1371/journal.pone.0127759. eCollection 2015. PLoS One. 2015. PMID: 26011525 Free PMC article.
-
Mechanical ventilation during cardiopulmonary resuscitation with intermittent positive-pressure ventilation, bilevel ventilation, or chest compression synchronized ventilation in a pig model.Crit Care Med. 2014 Feb;42(2):e89-95. doi: 10.1097/CCM.0b013e3182a63fa0. Crit Care Med. 2014. PMID: 24158168
-
The combination of chest compression synchronized ventilation and aortic balloon occlusion improve the outcomes of cardiopulmonary resuscitation in swine.Front Med (Lausanne). 2022 Dec 21;9:1057000. doi: 10.3389/fmed.2022.1057000. eCollection 2022. Front Med (Lausanne). 2022. PMID: 36619612 Free PMC article.
-
Cardiopulmonary resuscitation without ventilation.Crit Care Med. 2000 Nov;28(11 Suppl):N186-9. doi: 10.1097/00003246-200011001-00003. Crit Care Med. 2000. PMID: 11098942 Review.
-
[Ventilation during cardiopulmonary resuscitation (CPR). A literature study and analysis of ventilation strategies].Anaesthesist. 1997 Feb;46(2):133-41. doi: 10.1007/s001010050383. Anaesthesist. 1997. PMID: 9133175 Review. German.
Cited by
-
Chest compression synchronized ventilation during prolonged experimental cardiopulmonary resuscitation improves oxygenation but may cause pneumothoraces.Resusc Plus. 2025 Feb 28;22:100918. doi: 10.1016/j.resplu.2025.100918. eCollection 2025 Mar. Resusc Plus. 2025. PMID: 40161292 Free PMC article.
-
Airway management and ventilation techniques in resuscitation during advanced life support: an update.J Anesth Analg Crit Care. 2024 Aug 24;4(1):58. doi: 10.1186/s44158-024-00195-x. J Anesth Analg Crit Care. 2024. PMID: 39182146 Free PMC article. Review.
References
-
- Armstead WM, Hekierski H, Pastor P, Yarovoi S, Higazi AA, Cines DB. Release of IL-6 after stroke contributes to impaired cerebral autoregulation and hippocampal neuronal necrosis through NMDA receptor activation and upregulation of ET-1 and JNK. Translational Stroke Research. 2019;10(1):104–111. doi: 10.1007/s12975-018-0617-z. - DOI - PubMed
-
- Björklund E, Lindberg E, Rundgren M, Cronberg T, Friberg H, Englund E. Ischaemic brain damage after cardiac arrest and induced hypothermia–a systematic description of selective eosinophilic neuronal death. A neuropathologic study of 23 patients. Resuscitation. 2014;85(4):527–532. doi: 10.1016/j.resuscitation.2013.11.022. - DOI - PubMed
-
- Bro-Jeppesen JKJ, Wanscher M, Nielsen N, Friberg H, Bjerre M, Hassager C. Systemic inflammatory response and potential prognostic implications after out-of-hospital cardiac arrest: a substudy of the target temperature management trial. Critical Care Medicine. 2015;43(6):1223–1232. doi: 10.1097/CCM.0000000000000937. - DOI - PubMed
-
- Brower RG, Lanken PN, MacIntyre N, Matthay MA, Morris A, Ancukiewicz M, Schoenfeld D, Thompson BT. National Heart, Lung, and Blood Institute ARDS Clinical Trials Network Higher versus lower positive end-expiratory pressures in patients with the acute respiratory distress syndrome. The New England Journal of Medicine. 2004;351(4):327–336. doi: 10.1056/NEJMoa032193. - DOI - PubMed
-
- Brower RG, Matthay MA, Morris A, Schoenfeld D, Thompson BT, Wheeler A. Ventilation with lower tidal volumes as compared with traditional tidal volumes for acute lung injury and the acute respiratory distress syndrome. The New England Journal of Medicine. 2000;342(18):1301–1308. doi: 10.1056/NEJM200005043421801. - DOI - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous