Suppr超能文献

新型NMDA拮抗剂HU-211对沙土鼠全脑缺血的神经保护活性。

Neuroprotective activity of HU-211, a novel NMDA antagonist, in global ischemia in gerbils.

作者信息

Bar-Joseph A, Berkovitch Y, Adamchik J, Biegon A

机构信息

Pharmos Corp., Kiryat Weizmann, Rehovot, Israel.

出版信息

Mol Chem Neuropathol. 1994 Oct-Dec;23(2-3):125-35. doi: 10.1007/BF02815406.

Abstract

HU-211, a nonpsychotropic cannabinoid and a noncompetitive NMDA antagonist, was tested in a global ischemia model in the Mongolian gerbil. Male Mongolian gerbils underwent a 10-min bilateral common carotid artery occlusion. HU-211, administered i.v. at 4 mg/kg, 30 min postischemia, induced statistically significant neuroprotection of the CA1 subfield of the hippocampus. A dose-response study demonstrated an inverted U curve in which the 4 mg/kg dose induced the best neuroprotection in the CA1 subfield of the hippocampus (p < 0.05 ANOVA followed by Duncan's post-hoc test). The therapeutic window was then investigated, and in another study, HU-211 4 mg/kg were administered i.v. at 30, 60, 120, and 180 min postinsult. A statistically significant neuroprotection was detected at 30 and 60 min administration postinsult.

摘要

HU-211是一种非精神活性大麻素和非竞争性N-甲基-D-天冬氨酸(NMDA)拮抗剂,在蒙古沙鼠的全脑缺血模型中进行了测试。雄性蒙古沙鼠接受了10分钟的双侧颈总动脉闭塞。在缺血后30分钟静脉注射4毫克/千克的HU-211,对海马CA1亚区产生了具有统计学意义的神经保护作用。一项剂量反应研究显示出倒U形曲线,其中4毫克/千克的剂量在海马CA1亚区诱导出最佳的神经保护作用(方差分析后进行邓肯事后检验,p < 0.05)。随后研究了治疗窗,在另一项研究中,在损伤后30、60、120和180分钟静脉注射4毫克/千克的HU-211。在损伤后30分钟和60分钟给药时检测到具有统计学意义的神经保护作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验