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Lycopene-Loaded Microemulsion Regulates Neurogenesis in Rats with Aβ-Induced Alzheimer’s Disease Rats Based on the Wnt/β-catenin Pathway
Author(s) -
Wenjing Ning,
Renjun Lv,
Ning Xu,
Xunyao Hou,
Chao Shen,
Yunliang Guo,
Zhongyu Fan,
Na Cao,
Xueping Liu
Publication year - 2021
Publication title -
neural plasticity
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.288
H-Index - 68
eISSN - 2090-5904
pISSN - 1687-5443
DOI - 10.1155/2021/5519330
Subject(s) - neurogenesis , morris water navigation task , dentate gyrus , neun , hippocampus , wnt signaling pathway , chemistry , biology , medicine , endocrinology , microbiology and biotechnology , signal transduction , immunohistochemistry
Objective To investigate the effects of lycopene-loaded microemulsion (LME) on the cognitive function and neurogenesis in the dentate gyrus (DG) of the hippocampus and subventricular (SVZ) region of rats with amyloid β - (A β -) induced Alzheimer's disease (AD) and its mechanism based on the Wnt/ β -catenin pathway.Methods Healthy Wistar rats were divided into four groups: the blank control (CON), AD control, traditional lycopene (LOO), and LME groups. The CON and AD groups were fed with normal saline, while the LOO group was fed with traditional lycopene, and the LME group was fed with lycopene-loaded microemulsion. Behavioral tests were performed after three weeks of gastric administration. Immunofluorescence-labeled cells were used to observe the differentiation and maturation of new nerve cells in the DG of the hippocampus and SVZ region. qRT-PCR and Western blotting detected the expression of neurogenesis genes and Wnt/ β -catenin pathway-related proteins, respectively.Results On the Morris water maze test, LME rats had significantly shortened movement trajectory on the searching platform, reduced escape latency time, and increased residence time on the original platform quadrant. In addition, more LME rats crossed the platform when it was removed. Thus, LME can improve the spatial learning and memory of A β -induced AD rats. On qRT-PCR, LME significantly increased Reelin, Nestin, and Pax6 gene expressions, which regulate neurogenesis. Immunofluorescence showed that LME could significantly increase BrdU + , Dcx + , BrdU + /Neun + , BrdU + /Dcx + cells in the DG and SVZ regions, thus promoting neurogenesis. LME also reduced the number of Iba1 + and Iba1 + /BrdU + cells, thus reducing the neuroinflammatory response. On Western blot, LME upregulated the Wnt/ β -catenin pathway by upregulating Wnt3a, β -catenin, Disheveled (Dvl), and p-GSK3 β and downregulating p- β -catenin and GSK3 β .Conclusion LME attenuates cognitive impairment in A β -induced AD rats by promoting neurogenesis in the hippocampus and SVZ region through upregulating the Wnt/ β -catenin pathway.

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