Puerarin promoted proliferation and differentiation of dopamine-producing cells in Parkinson’s animal models
[Display omitted] •In vitro, PR promotes the differentiation of TH+ cells from MSCs.•In vivo, PR promotes the survival of transplantated DA-producing cells.•In vivo, PR promoted the transplanted cells proliferated and differentiated into TH + cells. Parkinson’s disease (PD) is caused by the gradual...
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Published in | Biomedicine & pharmacotherapy Vol. 106; pp. 1236 - 1242 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
France
Elsevier Masson SAS
01.10.2018
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Subjects | |
Online Access | Get full text |
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Summary: | [Display omitted]
•In vitro, PR promotes the differentiation of TH+ cells from MSCs.•In vivo, PR promotes the survival of transplantated DA-producing cells.•In vivo, PR promoted the transplanted cells proliferated and differentiated into TH + cells.
Parkinson’s disease (PD) is caused by the gradual loss of dopamine-producing cells in the brain. This study evaluated the potential neuroprotective role of puerarin (PR) on dopamine (DA)-producing cells in vitro and in vivo.
In vitro, the effects of PR on proliferation and differentiation and DA releases of mesenchymal stem cells (MSCs) were assayed by CCK-8, flow cytometry, real-time PCR and ELISA respectively. Then the differentiated cells were labeled with enhanced green fluorescent protein (EGFP) and administrated into PD animal models induced by 6-OHDA. The proliferation and differentiation of labeled cells were identified by fluorescence microscopy and immunostaining.
In vitro, after being treated with different concentrations of PR for 1 week, the TUJ1, TH and DAT protein and mRNA expression and DA releases increased significantly. In vivo, after transplantation of PR-treated DA-producing cells, the symptoms of PD improved significantly from the second week after transplantation; more transplanted cells survived and migrated to wider region along injection line; more transplanted cells proliferated and differentiated into TH+ cells; more DA was detected in the striatum during 6 weeks’ observation.
The results suggest that PR promote DA neuron survival, proliferation and differentiation. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0753-3322 1950-6007 |
DOI: | 10.1016/j.biopha.2018.07.058 |