4.7 Review

Yuan-Hu Zhi Tong Prescription Mitigates Tau Pathology and Alleviates Memory Deficiency in the Preclinical Models of Alzheimer's Disease

Journal

FRONTIERS IN PHARMACOLOGY
Volume 11, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fphar.2020.584770

Keywords

Alzheimer’ s disease; P301S tau mice; neurofibrillary tangles; Chinese medicine; yuan-hu zhi tong; microarray; connectivity map

Funding

  1. Hong Kong Health and Medical Research Fund [HMRF 12132061, HMRF 14150811, HMRF 15163481, HMRF 17182541, HMRF 17182551]
  2. General Research Fund from Hong Kong Government SAR [GRF/HKBU 12101417, GRF/HKBU 12100618]
  3. Hong Kong Baptist University [HKBU/RC-IRCs/17-18/03]
  4. National Natural Science Foundation, China (NSFC) [81773926, 81703487]
  5. Shenzhen Science and Technology Innovation Commission, China [JCYJ20180507184656626, JCYJ20180302174028790]

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Alzheimer's disease (AD) is characterized by memory dysfunction, A beta plaques together with phosphorylated tau-associated neurofibrillary tangles. Unfortunately, the present existing drugs for AD only offer mild symptomatic cure and have more side effects. As such, developments of effective, nontoxic drugs are immediately required for AD therapy. Present study demonstrates a novel role of Chinese medicine prescription Yuan-Hu Zhi Tong (YZT) in treating AD, and it has substantiated the in vivo effectiveness of YZT in two different transgenic mice models of AD, namely P301S tau and 3XTg-AD mice. Oral treatment of YZT significantly ameliorates motor dysfunction as well as promotes the clearance of aggregated tau in P301S tau mice. YZT improves the cognitive function and reduces the insoluble tau aggregates in 3XTg-AD mice model. Furthermore, YZT decreases the insoluble AT8 positive neuron load in both P301S tau and 3XTg-AD mice. Using microarray and the Connectivity Map analysis, we determined the YZT-induced changes in expression of signaling molecules and revealed the potential mechanism of action of YZT. YZT might regulate ubiquitin proteasomal system for the degradation of tau aggregates. The research results show that YZT is a potential drug candidate for the therapy of tau pathogenesis and memory decline in AD.

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