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1.
Chinese Journal of Diabetes ; (12): 475-478, 2015.
Artículo en Chino | WPRIM | ID: wpr-464453

RESUMEN

[Summary] Sodium glucose cotransporter 2 (SGLT2) inhibitors have been developed as a new antidiabetic agent .The antihyperglycemic effect of SGLT 2 inhibitors is independent of insulin secretion and insulin action .SGLT2 inhibitors improve IS and islet βcell function with the possible mechanisms of reducing glucotoxicity ,weight loss and increasing GLP‐1 response .

2.
West China Journal of Stomatology ; (6): 286-290, 2013.
Artículo en Chino | WPRIM | ID: wpr-336337

RESUMEN

<p><b>OBJECTIVE</b>To investigate the effect of Porphyromonas gingivalis lipopolysaccharide (LPS) on proliferation and inflammatory factors expression of human periodontal ligament stem cells (HPDLSCs).</p><p><b>METHODS</b>HPDLSCs were cultivated and identified. Experiment was divided into 3 groups according to culture solution: Group A with alpha-MEM culture solution containing 10 microg.mL-1 LPS, group B with supernatant fluid containing 10ng.mL-1 LPS stimulated monocyte, group C with alpha-MEM culture solution. The proliferation ability of HPDLSCs was analyzed by MTF assay. The expression levels of interleukin-1beta (IL-1beta), interleukin-6 (IL-6), tumor necrosis factor (TNF-alpha) mRNA of HPDLSCs were detected by reverse transcriptase polymerase chain reaction(RT-PCR).</p><p><b>RESULTS</b>HPDLSCs had clonality, bone and fat differentiation ability. Compared with group C, the proliferation ability of HPDLSCs of group A and group B was significantly inhibited, and the proliferation ability of HPDLSCs of group B were more significantly inhibited than that of group A (P<0.05). The expression of IL-1beta, IL-6 and TNF-alpha mRNA of group A and group B increased compared with the control group, and the expression of IL-1beta, IL-6 and TNF-alpha mRNA of group B increased more than that of group A (P<0.05).</p><p><b>CONCLUSION</b>Porphyromonas gingivalis may inhibit the proliferation of HPDLSCs directly or indirectly through LPS and increase expression of inflammatory factor, exacerbate periodontal inflammatory tissue damage and delay the self-repairing of periodontal tissue.</p>


Asunto(s)
Humanos , Diferenciación Celular , Interleucina-1beta , Interleucina-6 , Lipopolisacáridos , Monocitos , Compuestos Orgánicos , Ligamento Periodontal , Porphyromonas gingivalis , ARN Mensajero , Células Madre , Factor de Necrosis Tumoral alfa
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