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预防性苯巴比妥钠对足月缺氧缺血性大鼠治疗性低温的影响。

The effects of adding prophylactic phenobarbital to therapeutic hypothermia in the term-equivalent hypoxic-ischemic rat.

机构信息

Department of Pediatrics, Weill Cornell Medical College, New York, New York.

Citigroup Biomedical Imaging Center, Weill Cornell Medical College, New York, New York.

出版信息

Pediatr Res. 2018 Feb;83(2):506-513. doi: 10.1038/pr.2017.266. Epub 2017 Nov 22.

Abstract

BackgroundHypoxic-ischemic encephalopathy (HIE) is a major cause of neonatal morbidity and mortality. Therapeutic hypothermia (TH) is the only available intervention, but neuroprotection is incomplete and variable. Seizures are common in infants with HIE undergoing TH and may worsen outcome. Phenobarbital (PB) is sometimes added, although use of prophylactic PB is controversial in the neonate. We hypothesize that prophylactic PB will not reduce, and may enhance, the neuroprotective effects of TH on brain injury and motor outcomes in the postnatal day 10 (P10) hypoxic-ischemic (HI) rat.MethodsP10 rat pups were subjected to unilateral HI and 4 h recovery with: normothermia (N); hypothermia (TH); and hypothermia with phenobarbital (TH+PB). Brain damage was assessed longitudinally at 24 h and 2 weeks using brain magnetic resonance imaging and 12 weeks using histochemical analysis. Motor function was assessed with the beam walk and cylinder tests.ResultsTH and TH+PB induced neuroprotection, as measured by global brain damage score and improved motor function. Exploratory analyses suggest that TH+PB may confer enhanced protection, especially to the extent of damage.ConclusionProphylactic PB with TH is not deleterious and may provide additional long-term neuroprotection, including improvement of motor outcomes following HI in the term-equivalent, neonatal rat.

摘要

背景

缺氧缺血性脑病(HIE)是新生儿发病率和死亡率的主要原因。治疗性低温(TH)是唯一可用的干预措施,但神经保护不完全且存在差异。接受 TH 的 HIE 婴儿常发生癫痫发作,且可能使预后恶化。苯巴比妥(PB)有时会添加,但在新生儿中预防性使用 PB 存在争议。我们假设预防性 PB 不会降低,甚至可能增强 TH 对 P10 缺氧缺血(HI)大鼠脑损伤和运动结果的神经保护作用。

方法

P10 大鼠幼仔接受单侧 HI 和 4 小时恢复:正常体温(N);低温(TH);低温加苯巴比妥(TH+PB)。使用脑磁共振成像在 24 小时和 2 周以及使用组织化学分析在 12 周评估脑损伤。使用光束行走和圆筒测试评估运动功能。

结果

TH 和 TH+PB 诱导神经保护,表现为全脑损伤评分降低和运动功能改善。探索性分析表明,TH+PB 可能提供增强的保护作用,尤其是在损伤程度方面。

结论

TH 预防性使用 PB 不仅无害,而且可能提供额外的长期神经保护作用,包括改善足月新生儿 HI 后的运动结果。

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