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3′-Daidzein sulfonate sodium improves mitochondrial functions after cerebral ischemia/reperfusion injury 被引量:10
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作者 Wa Yuan Qin Chen +4 位作者 Jing Zeng Hai Xiao Zhi-hua Huang Xiao Li Qiong Lei 《Neural Regeneration Research》 SCIE CAS CSCD 2017年第2期235-241,共7页
3′-Daidzein sulfonate sodium is a new synthetic water-soluble compound derived from daidzein(an active ingredient of the kudzu vine root). It has been shown to have a protective effect on cerebral ischemia/reperfus... 3′-Daidzein sulfonate sodium is a new synthetic water-soluble compound derived from daidzein(an active ingredient of the kudzu vine root). It has been shown to have a protective effect on cerebral ischemia/reperfusion injury in rats. We plan to study the mechanism of its protective effect. 3′-Daidzein sulfonate sodium was injected in rats after cerebral ischemia/reperfusion injury. Results showed that 3′-daidzein sulfonate sodium significantly reduced mitochondrial swelling, significantly elevated the mitochondrial membrane potential, increased mitochondrial superoxide dismutase and glutathione peroxidase activities, and decreased mitochondrial malondialdehyde levels. 3′-Daidzein sulfonate sodium improved the structural integrity of the blood-brain barrier and reduced blood-brain barrier permeability. These findings confirmed that 3′-daidzein sulfonate sodium has a protective effect on mitochondrial functions after cerebral ischemia/reperfusion injury, improves brain energy metabolism, and provides protection against blood-brain barrier damage. 展开更多
关键词 nerve regeneration 3′-daidzein sulfonate sodium cerebral ischemia/reperfusion injury infarct volume anti-oxidation mitochondria mitochondrial membrane swelling mitochondrial membrane potential superoxide dismutase malondialdehyde glutathione peroxidase blood-brain barrier neural regeneration
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Silencing the gene encoding C/EBP homologous protein lessens acute brain injury following ischemia/reperfusion 被引量:2
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作者 Fengzhang Wang Yuan Zhang +3 位作者 Chunke He Tingting Wang Qiyan Piao Qun Liu 《Neural Regeneration Research》 SCIE CAS CSCD 2012年第31期2432-2438,共7页
C/EBP homologous protein, an important transcription factor during endoplasmic reticulum stress, participates in cell apoptosis mediated by endoplasmic reticulum stress. Previous studies have shown that C/EBP homologo... C/EBP homologous protein, an important transcription factor during endoplasmic reticulum stress, participates in cell apoptosis mediated by endoplasmic reticulum stress. Previous studies have shown that C/EBP homologous protein mediates nerve injury during Alzheimer's disease, subarachnoid hemorrhage and spinal cord trauma. In this study, we introduced C/EBP homologous protein short hairpin RNA into the brains of ischemia/reperfusion rat models via injection of lentiviral vector through the left lateral ventricle. Silencing C/EBP homologous protein gene expression significantly reduced cerebral infarction volume, decreased water content and tumor necrosis factor-α and interleukin-1β mRNA expression in brain tissues following infarction, diminished the number of TUNEL-positive cells in the infarct region, decreased caspase-3 protein content and increased Bcl-2 protein content. These results suggest that silencing C/EBP homologous protein lessens cell apoptosis and inflammatory reactions, thereby protecting nerves. 展开更多
关键词 C/EBP homologous protein endoplasmic reticulum stress Alzheimer's disease subarachnoid hemorrhage tumor necrosis factor-α ischemia/reperfusion interleukin-1β cerebral infarction neural regeneration
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