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抗炎化合物坎地沙坦西立酯可改善新生鼠缺氧模型的神经结局。

The Anti-inflammatory Compound Candesartan Cilexetil Improves Neurological Outcomes in a Mouse Model of Neonatal Hypoxia.

机构信息

Department of Physiology and Medical Physics, Royal College of Surgeons in Ireland, Dublin, Ireland.

Division for Neurogeriatrics, Department of Neurobiology Care Sciences and Society, Center for Alzheimer Research, Karolinska Institutet, Stockholm, Sweden.

出版信息

Front Immunol. 2019 Jul 24;10:1752. doi: 10.3389/fimmu.2019.01752. eCollection 2019.

Abstract

Recent studies suggest that mild hypoxia-induced neonatal seizures can trigger an acute neuroinflammatory response leading to long-lasting changes in brain excitability along with associated cognitive and behavioral deficits. The cellular elements and signaling pathways underlying neuroinflammation in this setting remain incompletely understood but could yield novel therapeutic targets. Here we show that brief global hypoxia-induced neonatal seizures in mice result in transient cytokine production, a selective expansion of microglia and long-lasting changes to the neuronal structure of pyramidal neurons in the hippocampus. Treatment of neonatal mice after hypoxia-seizures with the novel anti-inflammatory compound candesartan cilexetil suppressed acute seizure-damage and mitigated later-life aggravated seizure responses and hippocampus-dependent learning deficits. Together, these findings improve our understanding of the effects of neonatal seizures and identify potentially novel treatments to protect against short and long-lasting harmful effects.

摘要

最近的研究表明,轻度缺氧诱导的新生儿癫痫发作可引发急性神经炎症反应,导致大脑兴奋性的持久变化,以及相关的认知和行为缺陷。在这种情况下,神经炎症的细胞成分和信号通路仍不完全清楚,但可能产生新的治疗靶点。在这里,我们表明,在小鼠中短暂的全脑缺氧诱导的新生儿癫痫发作导致细胞因子的短暂产生,小胶质细胞的选择性扩增以及海马锥体神经元的结构发生持久变化。在缺氧-癫痫发作后用新型抗炎化合物坎地沙坦西酯治疗新生小鼠,可抑制急性发作损伤,并减轻后期生活中加重的发作反应和海马依赖性学习缺陷。总的来说,这些发现提高了我们对新生儿癫痫发作影响的认识,并确定了潜在的新的治疗方法来预防短期和长期的有害影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4200/6667988/86d6813d72c4/fimmu-10-01752-g0001.jpg

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