首页> 外文期刊>Neurological Research: An Interdisciplinary Quarterly Journal >Reduced Nrf2 and Phase II enzymes expression in immune-mediated spinal cord motor neuron injury.
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Reduced Nrf2 and Phase II enzymes expression in immune-mediated spinal cord motor neuron injury.

机译:在免疫介导的脊髓运动神经元损伤中Nrf2和II期酶表达降低。

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摘要

The transcription factor nuclear factor erythroid 2 p45-related factor 2 (Nrf2), a major regulator of genes encoding Phase II detoxifying enzymes and antioxidant proteins, is important for protecting cells against oxidative damage. In this work, we report that in the immune-mediated motor neuron injury animal model, expression of Nrf2 and antioxidative enzymes including glutathione S-transferase, nicotinamide adenine dinucleotide phosphate (reduced)-quinone oxidoreductase 1 and heme oxygenase 1 were greatly reduced in motor neurons of spinal cord anterior horn in paralyzed guinea pigs, whereas the antioxidant enzymes in the dorsal horn of paralyzed guinea pigs were generally preserved. Our findings suggest that declined antioxidative capacity may contribute to the damage to motor neurons in the process of immune-mediated motor neuron injury. Although the exact mechanism of immune reactivity and Nrf2-antioxidant response element pathway inactivation remains to be elucidated, inducers of Phase II detoxification enzymes may be an attractive therapeutic target for immune-mediated motor neuron degeneration.
机译:转录因子核因子红系2 p45相关因子2(Nrf2)是编码II期解毒酶和抗氧化剂蛋白的基因的主要调节剂,对于保护细胞免受氧化损伤非常重要。在这项工作中,我们报告说,在免疫介导的运动神经元损伤动物模型中,Nrf2和抗氧化酶(包括谷胱甘肽S-转移酶,烟酰胺腺嘌呤二核苷酸磷酸(还原)-醌氧化还原酶1和血红素加氧酶1)的表达大大降低瘫痪的豚鼠的脊髓前角神经元,而瘫痪的豚鼠的背角的抗氧化酶通常被保留。我们的发现表明,抗氧化能力下降可能在免疫介导的运动神经元损伤过程中导致运动神经元损伤。尽管仍需要阐明免疫反应性和Nrf2-抗氧化剂反应元件途径失活的确切机制,但II期解毒酶的诱导剂可能是免疫介导的运动神经元变性的诱人治疗靶标。

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