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Gami-Chunghyuldan 可改善海马内注射 Aβ 1-42 寡聚体引起的记忆障碍和神经退行性变。

Gami-Chunghyuldan ameliorates memory impairment and neurodegeneration induced by intrahippocampal Aβ 1-42 oligomer injection.

机构信息

Department of Oriental Pharmaceutical Science, College of Pharmacy and Kyung Hee East-West Pharmaceutical Research Institute, Kyung Hee University, #1 Hoegi-dong, Dongdaemun-gu, Seoul 130-701, Republic of Korea.

出版信息

Neurobiol Learn Mem. 2011 Sep;96(2):306-14. doi: 10.1016/j.nlm.2011.06.004. Epub 2011 Jun 13.

DOI:10.1016/j.nlm.2011.06.004
PMID:21689771
Abstract

Soluble oligomeric forms of amyloid beta (AβO) are regarded as a main cause of synaptic and cognitive dysfunction in Alzheimer's disease (AD) and have been a primary target in the development of drug treatments for AD. The present study utilized a mouse model of AD induced by intrahippocampal injection of AβO (10 μM) to investigate the effects of Gami-Chunghyuldan (GCD), a standardized multi-herbal medicinal formula, on the presentation of memory deficits and neurohistological pathogenesis. GCD (10 and 50mg/kg/day, 5 days, p.o.) improved AβO-induced memory impairment as well as reduced neuronal cell death, astrogliosis, and microgliosis in the hippocampus. In addition, GCD prevented AβO-triggered synaptic disruption and cholinergic fiber loss. These results suggest that GCD may be useful in the prevention and treatment of AD.

摘要

可溶性寡聚体形式的淀粉样蛋白β(AβO)被认为是阿尔茨海默病(AD)中突触和认知功能障碍的主要原因,并且一直是 AD 药物治疗开发的主要目标。本研究利用 AβO(10 μM)海马内注射诱导的 AD 小鼠模型,探讨了加味参苓白术散(GCD),一种标准化的多草药配方,对记忆缺陷表现和神经组织病理学发病机制的影响。GCD(10 和 50mg/kg/天,5 天,口服)改善了 AβO 诱导的记忆障碍,并减少了海马中的神经元细胞死亡、星形胶质细胞增生和小胶质细胞增生。此外,GCD 防止了 AβO 引发的突触破坏和胆碱能纤维丢失。这些结果表明,GCD 可能有助于 AD 的预防和治疗。

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