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