A modified formulation of Huanglian-Jie-Du-Tang reduces memory impairments and β-amyloid plaques in a triple transgenic mouse model of Alzheimer's disease

被引:35
作者
Durairajan, Siva Sundara Kumar [1 ,2 ]
Iyaswamy, Ashok [1 ,2 ]
Shetty, Sravan Gopalakrishna [1 ,2 ]
Kammella, Ananth Kumar [1 ,2 ]
Malampati, Sandeep [1 ,2 ]
Shang, Wenbin [1 ,2 ]
Yang, Chuanbin [1 ,2 ]
Song, Juxian [1 ,2 ]
Chung, Sookja [3 ]
Huang, Jiandong [4 ]
Ilango, Kaliappan [5 ]
Han, Quan-Bin [6 ]
Li, Min [1 ,2 ]
机构
[1] Hong Kong Baptist Univ, Sch Chinese Med, Mr & Mrs Ko Chi Ming Ctr Parkinsons Dis Res, Neurosci Res Lab, Kowloon, Hong Kong, Peoples R China
[2] Hong Kong Baptist Univ, Sch Chinese Med, Mr & Mrs Ko Chi Ming Ctr Parkinsons Dis Res, Kowloon, Hong Kong, Peoples R China
[3] Univ Hong Kong, Li Ka Shing Fac Med, Dept Anat, Pokfulam Rd, Hong Kong, Hong Kong, Peoples R China
[4] Univ Hong Kong, Li Ka Shing Fac Med, Dept Biochem, Pokfulam Rd, Hong Kong, Hong Kong, Peoples R China
[5] SRM Univ, Interdisciplinary Inst Indian Syst Med, Phytochem & Anal Lab, Kattankulathur, Kancheepuram, India
[6] Hong Kong Baptist Univ, Sch Chinese Med, Nat Prod Chem & Anal Lab, Kowloon, Hong Kong, Peoples R China
来源
SCIENTIFIC REPORTS | 2017年 / 7卷
关键词
A-BETA; PROTEIN; BAICALIN; PRECURSOR; APP; BRAIN; PHOSPHORYLATION; TRANSLOCATION; DISCOVERY; DEFICITS;
D O I
10.1038/s41598-017-06217-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Alzheimer's disease (AD) is a degenerative disorder typified by progressive deterioration of memory and the appearance of beta-amyloid peptide (A beta)-rich senile plaques. Recently we have identified a novel function of a patented formulation of modified Huanglian-Jie-Tu-Tang (HLJDT-M), a Chinese herbal medicine, in treating AD in in vitro studies (US patent No. 9,375,457). HLJDT-M is a formulation composed of Rhizoma Coptitis, Cortex Phellodendri and Fructus Gardeniae without Radix Scutellariae. Here, we assessed the efficacy of HLJDT-M on a triple transgenic mouse model of AD (3XTg-AD). Oral administration of HLJDT-M ameliorated the cognitive dysfunction of 3XTg-AD mice and lessened the plaque burden. In addition, biochemical assays revealed a significant decrease in levels of detergentsoluble and acid-soluble A beta via decreasing the levels of full length amyloid-beta precursor protein (FL-APP) and C-terminal fragments of APP (CTFs) in brain lysates of HLJDT-M-treated mice. HLJDT-M treatment also significantly reduced the levels of FL-APP and CTFs in N2a/SweAPP cells. In contrast, treatment using the classical formula HLJDT did not reduce the memory impairment of 3XTg-AD mice and, rather, increased the A beta/Fl-APP/CTFs in both animal and cell culture studies. Altogether, our study indicates that HLJDT-M is a promising herbal formulation to prevent and/or cure AD.
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页数:13
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