PMID- 32902742 OWN - NLM STAT- MEDLINE DCOM- 20210602 LR - 20220119 IS - 1573-6903 (Electronic) IS - 0364-3190 (Linking) VI - 45 IP - 11 DP - 2020 Nov TI - Effect of Early Normobaric Hyperoxia on Blast-Induced Traumatic Brain Injury in Rats. PG - 2723-2731 LID - 10.1007/s11064-020-03123-x [doi] AB - Blast-induced traumatic brain injury (bTBI) is a leading cause of disability and mortality in soldiers during the conflicts in Iraq and Afghanistan. Although substantial clinical and animal studies have investigated the pathophysiology and treatments of bTBI, few effective therapies have been found, especially for the early rescue in the battlefield. The aim of this study is to evaluate neuroprotective effects of early normobaric hyperoxia (NBO) on bTBI. We established a rat model of bTBI caused by explosion in the cabin. It exhibited typical changes of mild bTBI, like impaired neurological function, brain edema, minor intracranial hemorrhage and neuron necrosis. The rats were divided into 4 groups (n = 12): Sham, Vehicle, hyperbaric oxygen (HBO) and NBO. Neurological function of the rats was assessed by the Neurological Severity Scores (NSS) at 24 h and 72 h after explosion. Serum interleukin-6 (IL-6), neuron specific enolase (NSE) and tau protein were measured at 24 h and 72 h after explosion. Brain water content was measured and Aquaporin-4 (AQP4) immunostaining was performed. Neuronal apoptosis was analyzed by TUNEL staining. NBO demonstrated curative effects on protecting the neurological function. Serum levels of NSE and tau protein were reduced at 24 h and 72 h after explosion. But the levels of IL-6 were not reduced significantly at both time points. Cerebral edema was alleviated. Simultaneously, AQP4 immunostaining of the hippocampus showed remarkably decreased expression after treatment. The number of apoptotic cells in hippocampus was also decreased. Compared with HBO, NBO is simple and convenient, and can be administered in remote areas. It may be a promising therapy for early rescue of bTBI in the battlefield. FAU - Li, Yanteng AU - Li Y AD - Department of Neurosurgery, Sixth Medical Center, Chinese PLA General Hospital, No. 6, Fucheng Road, Haidian District, Beijing, 100048, China. FAU - Lv, Wenying AU - Lv W AD - Department of Neurosurgery, Sixth Medical Center, Chinese PLA General Hospital, No. 6, Fucheng Road, Haidian District, Beijing, 100048, China. FAU - Cheng, Gang AU - Cheng G AD - Department of Neurosurgery, Sixth Medical Center, Chinese PLA General Hospital, No. 6, Fucheng Road, Haidian District, Beijing, 100048, China. FAU - Wang, Shuwei AU - Wang S AD - Department of Neurosurgery, Sixth Medical Center, Chinese PLA General Hospital, No. 6, Fucheng Road, Haidian District, Beijing, 100048, China. FAU - Liu, Bangxin AU - Liu B AD - Department of Neurosurgery, Central War Zone General Hospital of PLA, Wuhan, 430070, China. FAU - Zhao, Hulin AU - Zhao H AD - Department of Neurosurgery, Sixth Medical Center, Chinese PLA General Hospital, No. 6, Fucheng Road, Haidian District, Beijing, 100048, China. FAU - Wang, Hongwei AU - Wang H AD - Department of Neurosurgery, Sixth Medical Center, Chinese PLA General Hospital, No. 6, Fucheng Road, Haidian District, Beijing, 100048, China. FAU - Zhang, Leiming AU - Zhang L AD - Department of Neurosurgery, Sixth Medical Center, Chinese PLA General Hospital, No. 6, Fucheng Road, Haidian District, Beijing, 100048, China. FAU - Dong, Chao AU - Dong C AD - Department of Neurosurgery, Sixth Medical Center, Chinese PLA General Hospital, No. 6, Fucheng Road, Haidian District, Beijing, 100048, China. FAU - Zhang, Jianning AU - Zhang J AUID- ORCID: 0000-0002-1784-802X AD - Department of Neurosurgery, Sixth Medical Center, Chinese PLA General Hospital, No. 6, Fucheng Road, Haidian District, Beijing, 100048, China. jianningzhang2008@163.com. LA - eng GR - AHJ14J001/Major Projects of PLA Logistics/ GR - 81372128/Natural Science Foundation of China/ PT - Journal Article DEP - 20200909 PL - United States TA - Neurochem Res JT - Neurochemical research JID - 7613461 RN - 0 (Aqp4 protein, rat) RN - 0 (Aquaporin 4) RN - 0 (Il6 protein, rat) RN - 0 (Interleukin-6) RN - 0 (Mapt protein, rat) RN - 0 (tau Proteins) RN - EC 4.2.1.11 (Phosphopyruvate Hydratase) RN - S88TT14065 (Oxygen) SB - IM MH - Animals MH - Apoptosis/physiology MH - Aquaporin 4/metabolism MH - Blast Injuries/*therapy MH - Brain Injuries, Traumatic/*therapy MH - Explosions MH - Hippocampus/metabolism MH - Interleukin-6/metabolism MH - Male MH - Neuroprotection/*physiology MH - Oxygen/*therapeutic use MH - *Oxygen Inhalation Therapy MH - Phosphopyruvate Hydratase/metabolism MH - Rats, Sprague-Dawley MH - tau Proteins/metabolism OTO - NOTNLM OT - Blast injuries OT - Brain edema OT - Brain injuries OT - Normobaric hyperoxia OT - Rat EDAT- 2020/09/10 06:00 MHDA- 2021/06/03 06:00 CRDT- 2020/09/09 12:33 PHST- 2020/04/16 00:00 [received] PHST- 2020/09/03 00:00 [accepted] PHST- 2020/07/28 00:00 [revised] PHST- 2020/09/10 06:00 [pubmed] PHST- 2021/06/03 06:00 [medline] PHST- 2020/09/09 12:33 [entrez] AID - 10.1007/s11064-020-03123-x [pii] AID - 10.1007/s11064-020-03123-x [doi] PST - ppublish SO - Neurochem Res. 2020 Nov;45(11):2723-2731. doi: 10.1007/s11064-020-03123-x. Epub 2020 Sep 9.