会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 10. 发明申请
    • Neuroprotective effects of PPARy agonists against cellular oxidative insults
    • PPARγ激动剂对细胞氧化损伤的神经保护作用
    • US20040224995A1
    • 2004-11-11
    • US10435501
    • 2003-05-09
    • University of North Texas Health Science Center at Fort Worth
    • James W. SimpkinsPaul Aoun
    • A61K031/426
    • A61K31/426
    • The current invention comprises compositions and methods for protecting a neuronal cell of a subject from a toxic insult. The method includes delivering an effective amount of a neuroprotective compound to the neuronal cells before or after the toxic insult. The neuroprotective compounds contain a peroxisome proliferator activated receptor (nullPPAR-nullnull) binding moiety with either a phenolic ring moiety or a prostaglandin (nullPGnull) with a reactive null,null-unsaturated carbonyl group on the cyclopentenone ring. Other novel compounds are also disclosed. The toxic insult that impinges upon the neuronal cell may be an acute process, or chronic disease process. Oxidative stress (e.g. hydrogen peroxide, and glutamate), injury, and secondary physiological responses to injury are among the acute processes discussed. Clinical disease processes that comprise oxidative stress, inflammatory responses, strokes, Alzheimer's disease, dementia, and Parkinson's disease are also addressed. Because PPAR-null agonists are used to treat type II diabetes, a condition that leads to neurological complications, a single agent that can target both conditions is of great therapeutic value.
    • 本发明包括用于保护受试者的神经元细胞免受有毒侮辱的组合物和方法。 该方法包括在有毒侮辱之前或之后向神经元细胞递送有效量的神经保护性化合物。 神经保护性化合物含有在环戊烯酮环上具有反应性α,β-不饱和羰基的酚环部分或前列腺素(“PG”)的过氧化物酶体增殖物激活受体(“PPAR-γ”)结合部分。 还公开了其它新化合物。 撞击神经元细胞的毒性侮辱可能是急性过程或慢性疾病过程。 氧化应激(例如过氧化氢和谷氨酸盐),损伤和继发生的生理反应是讨论的急性过程。 还讨论了包括氧化应激,炎症反应,中风,阿尔茨海默病,痴呆和帕金森病的临床疾病过程。 因为PPAR-γ激动剂用于治疗II型糖尿病,导致神经系统并发症的病症,可以靶向两种病症的单一药物具有很大的治疗价值。