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1.
China Journal of Chinese Materia Medica ; (24): 2749-2753, 2017.
Article in Chinese | WPRIM | ID: wpr-256039

ABSTRACT

This paper was aimed to investigate the effect of Aralia echinocaulis containing serum on expression of β-catenin, Wnt-1, Frizzed-2, TCF and Axin in Wnt/β-catenin signaling pathway of primary osteoblasts. SD healthy female rats (n=80) were used to make A. echinocaulis containing serum by gastric perfusion for seven days with distilled water, A. echinocaulis decoction high dosage, middle dosage, and low dosage. In vitro, primary osteoblasts were cultured and identified. The third generation primary osteoblasts were taken and cultured for 48 h, then cells were treated with the different drug serums for 10 days and calcified nodules were counted by alizarin red staining. The cells were collected after treatment for 48 h and the expression levels of β-catenin, Wnt-1, Frizzled-2, TCF and Axin were detected by Real-time PCR and Western blot. The results suggested that the in vitro cells were primary osteoblasts; and after treatment, various doses groups could promote the mineralization ability of primary osteoblasts, up-regulate the mRNA and protein expression levels of β-catenin, Wnt-1, Frizzled-2, and TCF, and down-regulate the mRNA and protein expression levels of Axin. These findings indicated that A. echinocaulis containing serum can enhance the differentiation and proliferation of osteoblasts by regulating the expression levels of β-catenin, Wnt-1, Frizzled-2, TCF and Axin in Wnt/β-catenin signaling pathway of primary osteoblasts.

2.
China Journal of Orthopaedics and Traumatology ; (12): 761-765, 2011.
Article in Chinese | WPRIM | ID: wpr-347072

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the influence of aqueous extract of Aralia echinocaulis Hand.-Mazz on the expression of fracture healing-ralated factor receptors.</p><p><b>METHODS</b>Single factor model was set up in SD rat. Selecting 14 and 28 days in the experiment. Immunohistochemistry was employed to determine the expression of Fibroblast growth factor receptor 2 (FGFR2), Fms-like tyrosine kinase (Flt-1) and Fetal licer kinase (Flk-1) at 14 and 28 days after model establishing.</p><p><b>RESULTS</b>The expression of Flt-1 and Flk-1 at 14 days (the latter was more remarkable) were obviously promoted in High dose group of aqueous extract of Aralia echinocaulis Hand.-Mazz, and higher than that in normal group and model group. The expression of FGFR2 in the high dose group of Aralia echinocaulis Hand -Mazz was also promoted visibility, close to that in the compare group (traditional Chinese medicine), but higher than than in the model group. There was no significant difference among them. At 28 days, the expression of FGFR2, Flt-1 and Flk-1 in all groups decreased except normal group, and got higher expression in model groups than each control groups.</p><p><b>CONCLUSION</b>Aqueous extract of Aralia echinocaulis Hand.-Mazz can promote angiogenesis in fracture healing, improve the activity and aggregation of fibroblasts, osteoblasts and chondrocytes. It also helps to quicken ossification in the cartilage and promote fracture healing.</p>


Subject(s)
Animals , Female , Rats , Aralia , Chemistry , Drugs, Chinese Herbal , Chemistry , Pharmacology , Therapeutic Uses , Fibroblast Growth Factors , Metabolism , Immunohistochemistry , Rats, Sprague-Dawley , Vascular Endothelial Growth Factor A , Metabolism , Wound Healing
3.
China Journal of Orthopaedics and Traumatology ; (12): 187-189, 2008.
Article in Chinese | WPRIM | ID: wpr-323181

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effect of Astaxanthin on enhancing the function of anti-oxidative damage in osteoblast.</p><p><b>METHODS</b>MC3T3-E1 osteoblasts were randomly divided into five groups, including control group, model group, Astaxanthin group [low-dose (1 x 10(-7) mol/L), middle-dose (1 x 10(-6) mol/L), high-dose (1 x 10(-5) mol/L)], in which the activity of cells, activity of superoxide dismutase (SOD), the content of reactive oxygen species (ROS), lipid oxygen (LPO) and membrane fluidity were tested and compared.</p><p><b>RESULTS</b>Compared with Astaxanthin groups, the activity of cells, SOD activity and membrane fluidity in the model group were significantly decreased (P < 0.01). However, the contents of ROS and LPO were significantly raised (P < 0.01).</p><p><b>CONCLUSION</b>H2O2 can cause oxidative damage of MC3T3-E1 osteoblasts, but Astaxanthin can prevent or decrease its influence.</p>


Subject(s)
Animals , Mice , Antioxidants , Chemistry , Pharmacology , Cell Line , Hydrogen Peroxide , Metabolism , Lipid Peroxidation , Membrane Fluidity , Osteoblasts , Metabolism , Oxidative Stress , Reactive Oxygen Species , Metabolism , Superoxide Dismutase , Metabolism , Xanthophylls , Chemistry , Pharmacology
4.
China Journal of Orthopaedics and Traumatology ; (12): 613-616, 2008.
Article in Chinese | WPRIM | ID: wpr-263750

ABSTRACT

<p><b>OBJECTIVE</b>To study the influence of canthaxanthin on D-galactose induced osseous changes of rat.</p><p><b>METHODS</b>Forty-five six-week-old Wistar male rats were randomly divided into model group, canthaxanthin group and young control group. In addition, 15 sixteen-month-old Wistar male rats were used as old control group. Model group and canthaxanthin group were given injections of D-galactose for 5 months (20 mg/kg/once per-day) to cause aging of rat. Then routine osseous parameters were tested and compared among the 4 groups.</p><p><b>RESULTS</b>Compared with young control group, the BMD, parameters of structural mechanics and biomechanics, bone calcium, manganese, magnesium and the content of hydroxyproline in the model group decreased significantly (P < 0.01), however, the content of bone phosphorus, the activity of bone and serum ALP increased significantly (P < 0.01). Those changes of the model group were the same as the old control group,but the changes in the canthaxanthin group significantly differed with the model group (P < 0.01).</p><p><b>CONCLUSION</b>The high does of D-galactose intake can cause aging and osteoporosis at the same time in rat, but canthaxanthin can prevent and inhibit D-galactose induced osseous changes.</p>


Subject(s)
Animals , Male , Rats , Alkaline Phosphatase , Blood , Biomechanical Phenomena , Bone Density , Bone and Bones , Chemistry , Calcium , Canthaxanthin , Pharmacology , Galactose , Toxicity , Malondialdehyde , Blood , Rats, Wistar , Superoxide Dismutase , Blood
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