Multi-organ protection of ulinastatin in traumatic cardiac arrest model

Abstract Background Post-cardiac arrest syndrome, which has no specific curative treatment, contributes to the high mortality rate of victims who suffer traumatic cardiac arrest (TCA) and initially can be resuscitated. In the present study, we investigated the potential of ulinastatin to mitigate mu...

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Main Authors: Shaoyun Liu, Jiefeng Xu, Yuzhi Gao, Peng Shen, Senlin Xia, Zilong Li, Mao Zhang
Format: Article
Language:English
Published: BMC 2018-11-01
Series:World Journal of Emergency Surgery
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13017-018-0212-3
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spelling doaj-f1e8e909c2694d6ca0454c712400d81e2020-11-25T02:15:41ZengBMCWorld Journal of Emergency Surgery1749-79222018-11-011311810.1186/s13017-018-0212-3Multi-organ protection of ulinastatin in traumatic cardiac arrest modelShaoyun Liu0Jiefeng Xu1Yuzhi Gao2Peng Shen3Senlin Xia4Zilong Li5Mao Zhang6Department of Emergency Medicine, Second Affiliated Hospital, Zhejiang University School of MedicineDepartment of Emergency Medicine, Second Affiliated Hospital, Zhejiang University School of MedicineDepartment of Emergency Medicine, Second Affiliated Hospital, Zhejiang University School of MedicineDepartment of Emergency Medicine, Second Affiliated Hospital, Zhejiang University School of MedicineDepartment of Emergency Medicine, Second Affiliated Hospital, Zhejiang University School of MedicineDepartment of Emergency Medicine, Yuyao People’s Hospital, Medical School of Ningbo UniversityDepartment of Emergency Medicine, Second Affiliated Hospital, Zhejiang University School of MedicineAbstract Background Post-cardiac arrest syndrome, which has no specific curative treatment, contributes to the high mortality rate of victims who suffer traumatic cardiac arrest (TCA) and initially can be resuscitated. In the present study, we investigated the potential of ulinastatin to mitigate multiple organ injury after resuscitation in a swine TCA model. Methods Twenty-one male pigs were subjected to hemodynamic shock (40% estimated blood loss in 20 min) followed by cardiac arrest (electrically induced ventricular fibrillation) and respiratory suspension for 5 min, and finally manual resuscitation. At 5 min after resuscitation, pigs were randomized to receive 80,000 U/kg ulinastatin (n = 7) or the same volume of saline (n = 9) in the TCA group. Pigs in the sham group (n = 5) were not exposed to bleeding or cardiac arrest. At baseline and at 1, 3, and 6 h after the return of spontaneous circulation, blood samples were collected and assayed for tumor necrosis factor-alpha, interleukin 6, and other indicators of organ injury. At 24 h after resuscitation, pigs were sacrificed and apoptosis levels were assessed in samples of heart, brain, kidney, and intestine. Results One pig died in the ulinastatin group and one pig died in the TCA group; the remaining animals were included in the final analysis. TCA and resuscitation caused significant increases in multiple organ function biomarkers in serum, increases in tumor necrosis factor-alpha, and interleukin 6 in serum and increases in the extent of apoptosis in key organs. All these increases were lower in the ulinastatin group. Conclusion Ulinastatin may attenuate multiple organ injury after TCA, which should be explored in clinical studies.http://link.springer.com/article/10.1186/s13017-018-0212-3UlinastatinTraumatic cardiac arrestOrgan protectionCardiopulmonary resuscitationPost-resuscitationIschemia-reperfusion injury
collection DOAJ
language English
format Article
sources DOAJ
author Shaoyun Liu
Jiefeng Xu
Yuzhi Gao
Peng Shen
Senlin Xia
Zilong Li
Mao Zhang
spellingShingle Shaoyun Liu
Jiefeng Xu
Yuzhi Gao
Peng Shen
Senlin Xia
Zilong Li
Mao Zhang
Multi-organ protection of ulinastatin in traumatic cardiac arrest model
World Journal of Emergency Surgery
Ulinastatin
Traumatic cardiac arrest
Organ protection
Cardiopulmonary resuscitation
Post-resuscitation
Ischemia-reperfusion injury
author_facet Shaoyun Liu
Jiefeng Xu
Yuzhi Gao
Peng Shen
Senlin Xia
Zilong Li
Mao Zhang
author_sort Shaoyun Liu
title Multi-organ protection of ulinastatin in traumatic cardiac arrest model
title_short Multi-organ protection of ulinastatin in traumatic cardiac arrest model
title_full Multi-organ protection of ulinastatin in traumatic cardiac arrest model
title_fullStr Multi-organ protection of ulinastatin in traumatic cardiac arrest model
title_full_unstemmed Multi-organ protection of ulinastatin in traumatic cardiac arrest model
title_sort multi-organ protection of ulinastatin in traumatic cardiac arrest model
publisher BMC
series World Journal of Emergency Surgery
issn 1749-7922
publishDate 2018-11-01
description Abstract Background Post-cardiac arrest syndrome, which has no specific curative treatment, contributes to the high mortality rate of victims who suffer traumatic cardiac arrest (TCA) and initially can be resuscitated. In the present study, we investigated the potential of ulinastatin to mitigate multiple organ injury after resuscitation in a swine TCA model. Methods Twenty-one male pigs were subjected to hemodynamic shock (40% estimated blood loss in 20 min) followed by cardiac arrest (electrically induced ventricular fibrillation) and respiratory suspension for 5 min, and finally manual resuscitation. At 5 min after resuscitation, pigs were randomized to receive 80,000 U/kg ulinastatin (n = 7) or the same volume of saline (n = 9) in the TCA group. Pigs in the sham group (n = 5) were not exposed to bleeding or cardiac arrest. At baseline and at 1, 3, and 6 h after the return of spontaneous circulation, blood samples were collected and assayed for tumor necrosis factor-alpha, interleukin 6, and other indicators of organ injury. At 24 h after resuscitation, pigs were sacrificed and apoptosis levels were assessed in samples of heart, brain, kidney, and intestine. Results One pig died in the ulinastatin group and one pig died in the TCA group; the remaining animals were included in the final analysis. TCA and resuscitation caused significant increases in multiple organ function biomarkers in serum, increases in tumor necrosis factor-alpha, and interleukin 6 in serum and increases in the extent of apoptosis in key organs. All these increases were lower in the ulinastatin group. Conclusion Ulinastatin may attenuate multiple organ injury after TCA, which should be explored in clinical studies.
topic Ulinastatin
Traumatic cardiac arrest
Organ protection
Cardiopulmonary resuscitation
Post-resuscitation
Ischemia-reperfusion injury
url http://link.springer.com/article/10.1186/s13017-018-0212-3
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