Low-dose nitroglycerine improves outcome after cardiac arrest in rats

被引:3
|
作者
Ebmeyer, Uwe [1 ]
Esser, Torben [1 ]
Keilhoff, Gerburg [2 ]
机构
[1] Univ Magdeburg, Dept Anaesthesiol, D-39106 Magdeburg, Germany
[2] Univ Magdeburg, Inst Biochem & Cell Biol, D-39106 Magdeburg, Germany
关键词
Cardiac arrest; Hippocampus; Neurodegeneration; Nitroglycerine; Functional outcome; Resuscitation; GLOBAL CEREBRAL-ISCHEMIA; CARDIOPULMONARY-RESUSCITATION; NITRIC-OXIDE; BRAIN; MODEL; EPINEPHRINE; NITRATES; INJURY; REPERFUSION; VASOPRESSIN;
D O I
10.1016/j.resuscitation.2013.10.009
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objective: The aim of this study was to evaluate the outcome of intravenously applied nitroglycerine (NTG, 1 mu g kg (1) min (1) for 1 h) after resuscitation from an asphyxia cardiac arrest (ACA) insult. We hypothesized that NTG infused for 1 h after the return of spontaneous circulation (ROSC) would improve functional and neuro-morphological outcomes. Methods: Adult rats were subjected to 8 min of ACA followed by resuscitation. There were three treatment groups: ACA, ACA + NTG and sham operated. Vital and blood parameters were monitored during the 1 h post-resuscitation intensive care phase. After survival times of 3, 6, 12, 24, 72 h and 7 days, the neurological deficit score (NDS) was measured. Histological evaluation of the hippocampus, cortex, the thalamic reticular nucleus and the caudate-putamen was performed 7 days post insult. Results: We found that NTG (i) induced significantly higher initial MAP peaks; (ii) resulted in a less-pronounced elevation of heart rates after ROSC with significantly faster normalization to baseline levels; and (iii) influenced glucose metabolism, temporarily elevating blood glucose to non-physiological levels. Even so, NTG (iv) improved the neurological outcome and (v) reduced neurodegeneration, mainly in the hippocampal CA1 region. A significant NTG-associated decrease in blood pressure did not occur. Conclusion: The effect of low-dosed NTG applied post-resuscitation appears to be neuroprotective, demonstrated by reduced hippocampal damage and a better NDS, even with temporarily elevated blood glucose to non-physiological levels. Thus, additional studies are needed to evaluate NTG-triggered mechanisms and optimized dosages before clinical translation should be considered. Animal study institutional protocol number: 42502-2-2-947-Uni-MD. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:276 / 283
页数:8
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