Neural Regeneration Research ›› 2017, Vol. 12 ›› Issue (2): 301-306.doi: 10.4103/1673-5374.200813

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Neuroprotective effect of the Chinese medicine Tiantai No. 1 and its molecular mechanism in the senescence-accelerated mouse prone

Ying-hong Li1, Xu-sheng Wang2, Xiao-lin Chen3, Yu Jin1, Hong-bo Chen4, Xiu-qin Jia1, Yong-feng Zhang1, Zheng-zhi Wu1   

  1. 1 First Affiliated Hospital of Shenzhen University (Shenzhen Second People’s Hospital), Shenzhen, Guangdong Province, China; 
    2 School of Life Sciences, Tsinghua University, Beijing, China; 
    3 Guangzhou Medical University, Guangzhou, Guangdong Province, China; 
    4 Shenzhen Key Laboratory of Health Sciences and Technology, Graduate School at Shenzhen, Tsinghua University, Beijing, China
  • Received:2016-12-28 Online:2017-02-15 Published:2017-02-15
  • Contact: Zheng-zhi Wu,yinghongli@163.com or szwzz001@163.com.
  • Supported by:

    This study was funded by the National Natural Science Foundation of China, No. 81473742; the Guangdong Science and Technology Foundation, No. 2013B021800101; the Shenzhen Major Project of Science and Technology Planning, No. JCYJ20130401115231337.

Abstract:

Tiantai No. 1, a Chinese medicine predominantly composed of powdered Rhizoma Gastrodiae, Radix Ginseng, and Ginkgo leaf at a ratio of 2:1:2 and dissolved in pure water, is neuroprotective in animal models of various cognitive disorders, but its molecular mechanism remains unclear. We administered Tiantai No. 1 intragastrically to senescence-accelerated mouse prone 8 (SAMP8) mice (a model of Alzheimer’s disease) at doses of 50, 100 or 150 mg/kg per day for 8 weeks and evaluated their behavior in the Morris water maze and expression of Alzheimer’s disease-related proteins in the brain. Tiantai No. 1 shortened the escape latency in the water maze training trials, and increased swimming time in the target quadrant during the spatial probe test, indicating that Tiantai No. 1 improved learning and memory in SAMP8 mice. Immunohistochemistry revealed that Tiantai No. 1 restored the proliferation potential of Ki67-positive cells in the hippocampus. In addition, mice that had received Tiantai No. 1 had fewer astrocytes, and less accumulation of amyloid-beta and phosphorylated tau. These results suggest that Tiantai No. 1 is neuroprotective in the SAMP8 mouse model of Alzheimer’s disease and acts by restoring neuronal number and proliferation potential in the hippocampus, decreasing astrocyte infiltration, and reducing the accumulation of amyloid-beta and phosphorylated tau.

Key words: nerve regeneration, neuroprotective effects, Alzheimer’s disease, Tiantai No. 1, SAMP8, amyloid-beta, autophagy-lysosome pathway,
ubiquitin proteasome pathway,
tau phosphorylation, neuronal apoptosis, astrocytosis, neural regeneration