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Biomed Res Int ; 2016: 9140541, 2016.
Article in English | MEDLINE | ID: mdl-27340670

ABSTRACT

The purpose of this study is to evaluate the therapeutic effects of human umbilical cord-derived mesenchymal stem cells (hUC-MSC) activated by curcumin (CUR) on PC12 cells induced by 1-methyl-4-phenylpyridinium ion (MPP+), a cell model of Parkinson's disease (PD). The supernatant of hUC-MSC and hUC-MSC activated by 5 µmol/L CUR (hUC-MSC-CUR) were collected in accordance with the same concentration. The cell proliferation and differentiation potential to dopaminergic neuronal cells and antioxidation were observed in PC12 cells after being treated with the above two supernatants and 5 µmol/L CUR. The results showed that the hUC-MSC-CUR could more obviously promote the proliferation and the expression of tyrosine hydroxylase (TH) and microtubule associated protein-2 (MAP2) and significantly decreased the expression of nitric oxide (NO) and inducible nitric oxide synthase (iNOS) in PC12 cells. Furtherly, cytokines detection gave a clue that the expression of IL-6, IL-10, and NGF was significantly higher in the group treated with the hUC-MSC-CUR compared to those of other two groups. Therefore, the hUC-MSC-CUR may be a potential strategy to promote the proliferation and differentiation of PD cell model, therefore providing new insights into a novel therapeutic approach in PD.


Subject(s)
Curcumin/therapeutic use , Mesenchymal Stem Cell Transplantation , Mesenchymal Stem Cells/cytology , Models, Biological , Parkinson Disease/therapy , Umbilical Cord/cytology , 1-Methyl-4-phenylpyridinium , Animals , Apoptosis/drug effects , Caspases/metabolism , Cell Differentiation/drug effects , Cell Proliferation/drug effects , Cell Separation , Curcumin/pharmacology , Cytokines/metabolism , Dopamine/metabolism , Dopamine Plasma Membrane Transport Proteins/metabolism , Humans , Mesenchymal Stem Cells/drug effects , Neurons/cytology , Neurons/drug effects , Neurons/enzymology , Nitric Oxide/metabolism , Nitric Oxide Synthase Type II/metabolism , PC12 Cells , Parkinson Disease/drug therapy , Proto-Oncogene Proteins c-bcl-2/metabolism , Rats , Tyrosine 3-Monooxygenase/metabolism
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