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首页> 外文期刊>Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research >Ginsenoside Re protects against phencyclidine-induced behavioral changes and mitochondrial dysfunction via interactive modulation of glutathione peroxidase-1 and NADPH oxidase in the dorsolateral cortex of mice
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Ginsenoside Re protects against phencyclidine-induced behavioral changes and mitochondrial dysfunction via interactive modulation of glutathione peroxidase-1 and NADPH oxidase in the dorsolateral cortex of mice

机译:人参皂甙重新保护谷胱甘肽过氧化物酶-1和小鼠背侧皮质中的谷胱甘肽过氧化物酶-1和NADPH氧化酶的相互作用调节和线粒体功能障碍。

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Abstract We investigated whether ginsenoside Re (Re) modulates phencyclidine (PCP)-induced sociability deficits and recognition memory impairments to extend our recent finding. We examined the role of GPx-1 gene in the pharmacological activity of Re against mitochondrial dysfunction induced by PCP in the dorsolateral cortex of mice. Since mitochondrial oxidative stress activates NADPH oxidase (PHOX), we applied PHOX inhibitor apocynin for evaluating interactive modulation between GPx-1 and PHOX against PCP neurotoxicity. Sociability deficits and recognition memory impairments induced by PCP were more pronounced in GPx-1 knockout (KO) than in wild type (WT) mice. PCP-induced mitochondrial oxidative stress, mitochondrial dysfunction, and membrane translocation of p47 phox were more evident in GPx-1 KO than in WT. Re treatment significantly attenuated PCP-induced neurotoxic changes. Re also significantly attenuated PCP-induced sociability deficits and recognition memory impairments. The attenuation by Re was comparable to that by apocynin. The attenuation was more obvious in GPx-1 KO than in WT. Importantly, apocynin did not show any additional positive effects on the neuroprotective activity of Re, indicating that PHOX is a molecular target for therapeutic activity of Re. Our results suggest that Re requires interactive modulation between GPx activity and PHOX (p47 phox ) to exhibit neuroprotective potentials against PCP insult. Graphical abstract Display Omitted Highlights ? Genetic depletion of GPx-1 facilitates PCP-induced mitochondrial dysfunction, oxidative parameters and PHOX activity. ? Genetic depletion of GPx-1 facilitates sociability deficits and recognition memory impairments induced by PCP. ? Re-mediated protective potentials against PCP required the interactive modulation between GPx-1 and PHOX (p47 phox ).
机译:摘要我们调查了人参皂苷Re(RE)调节了Phentyclidine(PCP) - 诱导社交件缺陷和识别记忆障碍,以扩展我们最近的发现。我们研究了GPX-1基因在对小鼠背侧皮质中PCP诱导的RE针对线粒体功能障碍的药理活性的作用。由于线粒体氧化应激激活NADPH氧化酶(PHOX),因此我们将PHOX抑制剂呼吸皂苷蛋白应用于评估GPX-1和PHOX之间的相互作用调节,对抗PCP神经毒性。 PCP诱导的社交赤字和识别记忆障碍在GPX-1敲除(KO)中比野生型(WT)小鼠更加明显。 PCP诱导的线粒体氧化应激,线粒体功能障碍和P47 PHOX的膜易位在GPX-1KO中比wt更明显。再治疗显着减弱了PCP诱导的神经毒性变化。 RE也显着减弱了PCP引起的社交性赤字和识别记忆障碍。 Re的衰减与Apocynin相当。 GPX-1 KO衰减比wt更明显。重要的是,Apocynin没有对RE的神经保护活性表明任何额外的正面影响,表明PHOX是RE治疗活性的分子靶标。我们的研究结果表明,RE需要GPX活动与PHOX(P47 PHOX)之间的交互式调制,以表现出对PCP侮辱的神经保护潜力。图形抽象显示省略了亮点? GPX-1的遗传耗竭促进PCP诱导的线粒体功能障碍,氧化参数和PHOX活性。还GPX-1的遗传消耗促进了PCP诱导的社会性赤字和识别记忆障碍。还重新介导针对PCP的保护潜力需要GPX-1和PHOX(P47 PHOX)之间的交互式调节。

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