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Ginsenoside Rg1 can stimulate dental pulp stem cells to regenerate teeth

Ginsenoside Rb1 inhibits inflammation and release of inflammatory cytokines
Inflammation, which can be caused by pathogens like bacteria and viruses and non-infection factors such as poisons and disordered immune system, is a pathological process involved in many diseases. In non-infection inflammatory conditions, rheumatoid...
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Dental Pulp Stem Cells, or (DPSCs) are multipotent stem cells that have the potential to differentiate into a variety of cell types, including cells producing Bone and tissue in the oral cavity. Also, there are various studies where, through the stimulation of tissue-specific cytokines, these cells can differentiate into a variety of other cell types including 1) myocardiocytes to repair damaged cardiac tissue following a heart attack, 2) neuron to generate nerve and brain tissue, 3) osteocytes to generate bone, 4) chondrocytes to generate cartilage, etc. Therefore, dental pulp stem cells have a variety of clinical applications.

When dental pulp stem cells were treated with ginsenosides Rg1 and a BMP-2 (bone morphogenetic protein-2), these cells differentiated and produced dentin, making tooth regeneration possible. The finding was published by scientists in Chongqing Medical University on Laser Journal, 2012, volume 33, issue 3.

Title: Effect of ginsenoside Rgl and recombinant bone morphogenetic protein 2 on differentiation of human dental pulp stem cells in vitro
Laser Journal , 2012(03)
Abstract:
Objective: The aim of the present study is to evaluate the effect of ginsenoside Rg1 and recombinant bone morphogenetic protein 2(rhBMP-2) on the differentiation of human dental pulp stem cells(DPSCs).

Methods: DPSCs were isolated and cultured.The cells were incubated with different concentrations of ginsenoside Rg1(0.1,0.5,2.5,5,10,20μmol/L) and rhBMP-2(25,50,100和200 ng/ml).The effect on the differentiation of DPSCs was assayed by ALP enzymatic activity,and the gene expression of dentin sialophosphoprotein(DSPP) and dentin matrix protein 1(DMP1) by real time RT-PCR.

Results: Comparing with the control group, ALP activity (alkaline phosphatase is particularly concentrated in bone and teeth) was significantly enhanced in ginsenoside Rgl(2.5,5,and 10μmol/L) group(P<0.001), especially in ginsenoside Rgl(5μmol/L) group. ALP activity was significantly enhanced in rhBMP-2(50,100,200 ng/ml) group,especially in rhBMP-2(100 ng/ml) group. The gene expression of DSPP and DMP1 were significantly increased in the combination group of ginsenoside Rgl(5μmol/L) and rhBMP-2(100 ng/ml) compared with single application of ginsenoside Rgl or rhBMP-2 only at the same time points(P < 0.001).

Conclusion: The results indicate that ginsenoside Rgl promotes the differentiation of DPSCs.Combined application of ginsenoside Rgl and rhBMP2 can greatly promote DPSCs differentiation.

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