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首页> 外文期刊>Toxicology and Industrial Health >Neuroprotective effect of ebselen against intracerebroventricular streptozotocin-induced neuronal apoptosis and oxidative stress in rats
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Neuroprotective effect of ebselen against intracerebroventricular streptozotocin-induced neuronal apoptosis and oxidative stress in rats

机译:依布硒啉对大鼠脑室内链脲佐菌素诱导的神经元凋亡和氧化应激的神经保护作用

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The goal of this study was to examine the neuroprotective effect of ebselen against intracerebroventricular streptozotocin (ICV-STZ)-induced oxidative stress and neuronal apoptosis in rat brain. A total of 30 adult male Sprague-Dawley rats were randomly divided into 3 groups of 10 animals each: control, ICV-STZ, and ICV-STZ treated with ebselen. The ICV-STZ group rats were injected bilaterally with ICV-STZ (3 mg/kg) on days 1 and 3, and ebselen (10 mg/kg/day) was administered for 14 days starting from 1st day of ICV-STZ injection to day 14. Rats were killed at the end of the study and brain tissues were removed for biochemical and histopathological investigation. Our results demonstrated, for the first time, the neuroprotective effect of ebselen on Alzheimer's disease (AD) model in rats. Our present study, in ICV-STZ group, showed significant increase in tissue malondialdehyde levels and significant decrease in enzymatic antioxidants superoxide dismutase and glutathione peroxidase in the frontal cortex tissue. The histopathological studies in the brain of rats also supported that ebselen markedly reduced the ICV-STZ-induced histopathological changes and well preserved the normal histological architecture of the frontal cortex tissue. The number of apoptotic neurons was increased in frontal cortex tissue after ICV-STZ administration. Treatment of ebselen markedly reduced the number of degenerating apoptotic neurons. The study demonstrates the effectiveness of ebselen, as a powerful antioxidant, in preventing the oxidative damage and morphological changes caused by ICV-STZ in rats. Thus, ebselen may have a therapeutic value for the treatment of AD.
机译:这项研究的目的是检查依布硒啉对大鼠脑室内脑室链脲佐菌素(ICV-STZ)诱导的氧化应激和神经元凋亡的神经保护作用。将总共​​30只成年雄性Sprague-Dawley大鼠随机分为3组,每组10只动物:对照,ICV-STZ和用依布硒仑处理的ICV-STZ。从第1天和第3天开始,向ICV-STZ组大鼠双侧注射ICV-STZ(3 mg / kg),并从注射ICV-STZ的第一天起,依伯硒仑(10 mg / kg / day)给药14天。第14天。在研究结束时处死大鼠,取出脑组织进行生化和组织病理学研究。我们的结果首次证明依布硒仑对大鼠阿尔茨海默氏病(AD)模型的神经保护作用。我们目前在ICV-STZ组的研究显示额叶皮层组织中丙二醛水平显着增加,酶促抗氧化剂超氧化物歧化酶和谷胱甘肽过氧化物酶显着降低。在大鼠脑中的组织病理学研究还支持依伯硒仑显着减少了ICV-STZ诱导的组织病理学变化,并很好地保留了额叶皮层组织的正常组织学结构。给予ICV-STZ后,额叶皮层组织中凋亡神经元的数量增加。依卜硒仑的治疗显着减少了退化性凋亡神经元的数量。这项研究表明依布硒啉是一种强大的抗氧化剂,可有效预防ICV-STZ引起的大鼠氧化损伤和形态变化。因此,依布硒仑对AD的治疗可能具有治疗价值。

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