Antonova Viktoriya V, Silachev Denis N, Plotnikov Egor Y, Pevzner Irina B, Yakupova Elmira I, Pisarev Mikhail V, Boeva Ekaterina A, Tsokolaeva Zoya I, Lyubomudrov Maxim A, Shumov Igor V, Grechko Andrey V, Grebenchikov Oleg A
Federal Research and Clinical Center of Intensive Care Medicine and Rehabilitology, Moscow 107031, Russia.
A.N. Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow 119992, Russia.
Biomedicines. 2024 Mar 13;12(3):635. doi: 10.3390/biomedicines12030635.
This is the first in vivo study to investigate the neuroprotective effects of krypton on focal cerebral ischemia. The aim of the study was to analyze the effect of 2 h of inhalation of a krypton-oxygen mixture (Kr 70%/O 30%) on the recovery of neurological functions and the degree of brain damage in rats after photoinduced ischemic stroke (PIS) and to investigate the possible mechanisms responsible for this neuroprotection. Experiments were performed on male Wistar rats weighing 250-300 g (n = 32). Animals were randomized into four groups. Two groups (n = 20) underwent photoinduced ischemic stroke, followed by 2 h of inhalation of krypton-oxygen mixture consisting of Kr 70%/O 30% or a nitrogen-oxygen breathing mixture consisting of N 70%/O 30%, followed by neurological examinations on days 3 and 7. The other two groups (n = 12) received only gas mixtures of the same concentration and exposure duration as in those in the PIS groups, then Western blot analysis of the potential molecular mechanisms was performed. The results of the study show that treatment with the krypton-oxygen mixture consisting of Kr 70%/O 30% improves the neurological status on day 7 of observation, reduces the lesion volume according to the MRI examination and the number of Iba-1- and caspase-3-positive cells in the damaged area, promotes the activation of neoangiogenesis (an increase in the von Willebrand factor), and reduces the penumbra area and the number of NeuN-positive cells in it on day 14 of observation. Inhalation of the krypton-oxygen mixture also significantly increases the levels of phosphorylated AKT kinase (protein kinase B) and glycogen synthase kinase 3b (pGSK3b) and promotes the expression of transcription factor Nrf2, which was accompanied by the lowered expression of transcription factor NFkB (p50). Thus, we showed pronounced neuroprotection induced by krypton inhalation after stroke and identified the signaling pathways that may be responsible for restoring neurological functions and reducing damage.
这是第一项研究氪对局灶性脑缺血神经保护作用的体内研究。该研究的目的是分析吸入氪 - 氧混合物(Kr 70%/O 30%)2小时对光诱导缺血性卒中(PIS)后大鼠神经功能恢复和脑损伤程度的影响,并研究这种神经保护作用的可能机制。实验在体重250 - 300克的雄性Wistar大鼠(n = 32)身上进行。动物被随机分为四组。两组(n = 20)接受光诱导缺血性卒中,随后吸入由Kr 70%/O 30%组成的氪 - 氧混合物或由N 70%/O 30%组成的氮 - 氧呼吸混合物2小时,然后在第3天和第7天进行神经学检查。另外两组(n = 12)仅接受与PIS组相同浓度和暴露时间的气体混合物,然后进行潜在分子机制的蛋白质印迹分析。研究结果表明,用Kr 70%/O 30%组成的氪 - 氧混合物治疗可改善观察第7天的神经状态,根据MRI检查减少病变体积以及受损区域中Iba - 1和caspase - 3阳性细胞的数量,促进新生血管生成的激活(血管性血友病因子增加),并减少观察第14天的半暗带区域及其内NeuN阳性细胞的数量。吸入氪 - 氧混合物还显著增加磷酸化AKT激酶(蛋白激酶B)和糖原合酶激酶3b(pGSK3b)的水平,并促进转录因子Nrf2的表达,同时伴随着转录因子NFkB(p50)表达的降低。因此,我们显示了卒中后吸入氪诱导的明显神经保护作用,并确定了可能负责恢复神经功能和减少损伤的信号通路。