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首页> 外文期刊>Pediatric Research >Partial Neuroprotective Effect of Pretreatment with Tanshinone IIA on Neonatal Hypoxia-Ischemia Brain Damage
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Partial Neuroprotective Effect of Pretreatment with Tanshinone IIA on Neonatal Hypoxia-Ischemia Brain Damage

机译:丹参酮IIA预处理对新生儿缺氧缺血性脑损伤的部分神经保护作用

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Tanshinone IIA is a compound purified from the Chinese herb Danshen (Radix Salviae Miltiorrhiza Bge). The neuroprotective effect of tanshinone IIA was investigated in a neonatal rat model of hypoxia-ischemia brain damage. Hypoxia-ischemia encephalopathy was induced in rats at day 7 of postnatal age by ligation of the right common carotid artery, followed by 2 h of hypoxia. Tanshinone IIA (10 mg/kg, i.p.) was injected daily from day 2 before surgery for 9 or 16 d. Our results demonstrated significant and sustained brain damage in the hypoxia-ischemia– and vehicle-treated groups at 1 and 3 wk after surgery. Treatment with tanshinone IIA significantly reduced the severity of brain injury, as indicated by the increase in ipsilateral brain weight and neuron density, compared with those of sham-operated animals. The recovery of sensorimotor function and histology was observed in animals that received tanshinone IIA. The plasma of tanshinone IIA–treated rats exhibited higher antioxidant activities, as reflected by the oxygen radical absorbance capacity assay, compared with the vehicle-treated rats. In the neural progenitor cell line C17.2 that was subjected to 2,2′-azobis (2-amidino propane hydrochloride)–induced oxidative stress, tanshinone IIA increased cell viability and protected against mitochondrial damage (JC-1 assay). Our results suggest that tanshinone IIA has antioxidative activities and that treatment that is started before a hypoxic-ischemic insult is partially neuroprotective. Further studies are required to elucidate whether rescue treatment with tanshinone IIA is effective and to determine whether its protective effect is also associated with secondary cooling of the brain.Abbreviations: AAPH, 2,2′-azobis (2-amidino propane hydrochloride); AchE, acetylcholinesterase; HIE, hypoxia-ischemia encephalopathy; MTT, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide; NSE, neuron-specific enolase; ORAC, oxygen radical absorbance capacity
机译:丹参酮IIA是从中药丹参(Radis Salviae Miltiorrhiza Bge)中纯化得到的化合物。在新生鼠缺氧缺血性脑损伤模型中研究了丹参酮IIA的神经保护作用。结扎右颈总动脉,然后缺氧2 h,在出生后第7天诱导大鼠缺氧缺血性脑病。从手术前第二天开始每天注射丹参酮IIA(10 mg / kg,腹腔注射),持续9或16天。我们的研究结果表明,缺氧缺血和溶媒治疗组在术后1周和3周出现了明显且持续的脑损伤。与假手术动物相比,丹参酮IIA治疗可显着降低脑损伤的严重程度,同侧大脑重量和神经元密度增加表明。在接受丹参酮IIA的动物中观察到感觉运动功能和组织学的恢复。丹参酮IIA处理的大鼠的血浆显示出比溶媒治疗的大鼠更高的抗氧化活性,这通过氧自由基吸收能力测定法得以反映。在受到2,2'-偶氮双(2-2-基丙烷盐酸盐)诱导的氧化应激的神经祖细胞系C17.2中,丹参酮IIA可提高细胞活力并保护其免受线粒体损害(JC-1分析)。我们的结果表明,丹参酮IIA具有抗氧化活性,在缺氧缺血性损伤之前开始的治疗具有部分神经保护作用。需要进一步的研究以阐明丹参酮IIA的抢救治疗是否有效,并确定其保护作用是否还与大脑的继发性冷却有关。 AchE,乙酰胆碱酯酶; HIE,缺氧缺血性脑病; MTT,3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四唑; NSE,神经元特异性烯醇化酶; ORAC,氧自由基吸收能力

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