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新型肌肽酰肼衍生物对短暂性脑缺血后海马 CA1 损伤的神经保护作用。

Neuroprotective effects of a novel carnosine-hydrazide derivative on hippocampal CA1 damage after transient cerebral ischemia.

机构信息

Department of Neurosurgery, Kurume University, School of Medicine, Fukuoka, Japan.

Department of Bioorganic and Medicinal Chemistry, Kumamoto University, Kumamoto, Japan; Department of Medicinal Chemistry, Faculty of Pharmacy, Minia University, Minia, Egypt.

出版信息

Eur J Med Chem. 2019 Feb 1;163:207-214. doi: 10.1016/j.ejmech.2018.11.060. Epub 2018 Nov 28.

Abstract

Ischemia-reperfusion injuries produce reactive oxygen species that promote the peroxide lipid oxidation process resulting in the production of an endogenic lipid peroxide, 4-hydroxy-trans-2-nonenal (4-HNE), a highly cytotoxic aldehyde that induces cell death. We synthesized a novel 4-HNE scavenger - a carnosine-hydrazide derivative, l-carnosine hydrazide (CNN) - and examined its neuroprotective effect in a model of transient ischemia. PC-12 cells were pre-incubated with various doses (0-50 mmol/L) of CNN for 30 min, followed by incubation with 4-HNE (250 μM). An MTT assay was performed 24 h later to examine cell survival. Transient ischemia was induced by bilateral common carotid artery occlusion (BCCO) in the Mongolian gerbil. Animals were assigned to sham-operated (n = 6), placebo-treated (n = 12), CNN pre-treated (20 mg/kg; n = 12), CNN post-treated (100 mg/kg; n = 11), and histidyl hydrazide (a previously known 4-HNE scavenger) post-treated (100 mg/kg; n = 7) groups. Heat shock protein 70 immunoreactivity in the hippocampal CA1 region was evaluated 24 h later, while delayed neuronal death using 4-HNE staining was evaluated 7 days later. Pre-incubation with 30 mmol/L CNN completely inhibited 4-HNE-induced cell toxicity. CNN prevented delayed neuronal death by >60% in the pre-treated group (p < 0.001) and by >40% in the post-treated group (p < 0.01). Histidyl hydrazide post-treatment elicited no protective effect. CNN pre-treatment resulted in high heat shock protein 70 and low 4-HNE immunoreactivity in CA1 pyramidal neurons. Higher 4-HNE immunoreactivity was also found in the placebo-treated animals than in the CNN pre-treated animals. Our novel compound, CNN, elicited highly effective 4-HNE scavenging activity in vitro. Furthermore, CNN administration both pre- and post-BCCO remarkably reduced delayed neuronal death in the hippocampal CA1 region via its induction of heat shock protein 70 and scavenging of 4-HNE.

摘要

缺血再灌注损伤产生活性氧,促进过氧化物脂质氧化过程,导致内源性脂质过氧化物 4-羟基-trans-2-壬烯醛(4-HNE)的产生,4-HNE 是一种高度细胞毒性的醛,可诱导细胞死亡。我们合成了一种新型的 4-HNE 清除剂——肌肽酰肼衍生物,L-肌肽酰肼(CNN),并在短暂性缺血模型中研究了其神经保护作用。PC-12 细胞用不同剂量(0-50mmol/L)的 CNN 预孵育 30min,然后用 4-HNE(250μM)孵育。24h 后进行 MTT 检测以检测细胞存活率。通过双侧颈总动脉闭塞(BCCO)在蒙古沙鼠中诱导短暂性缺血。动物被分为假手术组(n=6)、安慰剂组(n=12)、CNN 预处理组(20mg/kg;n=12)、CNN 后处理组(100mg/kg;n=11)和组氨酸酰肼(先前已知的 4-HNE 清除剂)后处理组(100mg/kg;n=7)。24h 后评估海马 CA1 区热休克蛋白 70 免疫反应性,7 天后用 4-HNE 染色评估迟发性神经元死亡。30mmol/L CNN 预孵育可完全抑制 4-HNE 诱导的细胞毒性。CNN 预处理组(p<0.001)和后处理组(p<0.01)可使迟发性神经元死亡分别减少>60%和>40%。组氨酸酰肼后处理无保护作用。CNN 预处理可使 CA1 锥体神经元中的热休克蛋白 70 高、4-HNE 免疫反应性低。与 CNN 预处理动物相比,安慰剂处理动物的 4-HNE 免疫反应性更高。我们的新型化合物 CNN 在体外具有高效的 4-HNE 清除活性。此外,BCCO 前后给予 CNN 可通过诱导热休克蛋白 70 和清除 4-HNE 来显著减少海马 CA1 区的迟发性神经元死亡。

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