Decoy compositions for treating and preventing brain diseases and disorders
    2.
    发明申请
    Decoy compositions for treating and preventing brain diseases and disorders 审中-公开
    用于治疗和预防脑部疾病和疾病的诱饵组合物

    公开(公告)号:US20080207552A1

    公开(公告)日:2008-08-28

    申请号:US11982970

    申请日:2007-11-05

    IPC分类号: A61K31/7088 A61P9/10

    摘要: The present invention provides introduction of NF-κB decoy oligodeoxynucleotide into rat cranial nerve through a carotid artery during global brain ischemia. Polymerase chain reaction demonstrated that one hour after global brain ischemia, transfected NF-κB decoy oligodeoxynucleotide effectively suppressed expression of tumor necrosis factor α, interleukin 1β and intracellular adhesion molecule 1 messenger RNAs. Terminal deoxynucleotidyl transferase-mediated deoxyuridine nick-end labeling staining and immunohistochemistry using microtubule-associated protein 2 demonstrated that transfected NF-κB decoy oligodeoxynucleotide significantly attenuated neuronal damage seven days after global brain ischemia. Therapeutic transfection of NF-κB decoy oligodeoxynucleotide during brain ischemia may be effective for attenuation of neuronal damage, suggesting a strategy for protecting the cerebrum from global ischemia.

    摘要翻译: 本发明提供了在全脑缺血期间通过颈动脉将NF-κB诱饵寡脱氧核苷酸引入大鼠颅神经中。 聚合酶链反应表明,全球脑缺血后1小时,转染的NF-κB诱饵寡脱氧核苷酸有效抑制肿瘤坏死因子α,白细胞介素1β和细胞内粘附分子1信使RNA的表达。 末端脱氧核苷酸转移酶介导的脱氧尿苷切口末端标记染色和使用微管相关蛋白2的免疫组织化学证实,转染的NF-κB诱饵寡脱氧核苷酸在全脑缺血后7天显着减弱神经元损伤。 在脑缺血期间,NF-κB诱饵寡脱氧核苷酸的治疗转染对于减少神经元损伤可能是有效的,这表明保护大脑免受全身缺血的策略。

    Decoy compositions for treating and preventing brain diseases and disorders
    3.
    发明申请
    Decoy compositions for treating and preventing brain diseases and disorders 审中-公开
    用于治疗和预防脑部疾病和疾病的诱饵组合物

    公开(公告)号:US20060135449A1

    公开(公告)日:2006-06-22

    申请号:US10509799

    申请日:2002-03-29

    IPC分类号: A61K48/00 A61K9/127

    摘要: The present invention provides introduction of NF-κB decoy oligodeoxynucleotide into rat cranial nerve through a carotid artery during global brain ischemia. Polymerase chain reaction demonstrated that one hour after global brain ischemia, transfected NF-κB decoy oligodeoxynucleotide effectively suppressed expression of tumor necrosis factor α, interleukin 1β and intracellular adhesion molecule 1 messenger RNAs. Terminal deoxynucleotidyl transferase-mediated deoxyuridine nick-end labeling staining and immunohistochemistry using microtubule-associated protein 2 demonstrated that transfected NF-κB decoy oligodeoxynucleotide significantly attenuated neuronal damage seven days after global brain ischemia. Therapeutic transfection of NF-κB decoy oligodeoxynucleotide during brain ischemia may be effective for attenuation of neuronal damage, suggesting a strategy for protecting the cerebrum from global ischemia.

    摘要翻译: 本发明提供了在全脑缺血期间通过颈动脉将NF-κB诱饵寡脱氧核苷酸引入大鼠颅神经中。 聚合酶链反应表明,全球脑缺血后1小时,转染的NF-κB诱饵寡脱氧核苷酸有效抑制肿瘤坏死因子α,白细胞介素1β和细胞内粘附分子1信使RNA的表达。 末端脱氧核苷酸转移酶介导的脱氧尿苷切口标记染色和使用微管相关蛋白2的免疫组织化学证实,转染的NF-κB诱饵寡脱氧核苷酸在全脑缺血后7天显着减弱神经元损伤。 在脑缺血期间,NF-κB诱饵寡脱氧核苷酸的治疗转染对于减少神经元损伤可能是有效的,这表明保护大脑免受全身缺血的策略。