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1.
Sichuan Da Xue Xue Bao Yi Xue Ban ; 43(3): 367-72, 2012 May.
Article in Chinese | MEDLINE | ID: mdl-22812239

ABSTRACT

OBJECTIVE: To investigate the effect of sinusoidal electricity magnetic fields (SEMFs) on the proliferation and differentiation of osteoblasts in vitro. METHODS: Calvarial osteoblasts of newborn rats were isolated by enzyme digestion and randomly divided into 3 groups after subculture. Two groups of cells were exposed to 50 Hz 1.8 mT SEMFs for 30 min/d in parallel and vertical, respectively. Those without SEMFs exposure served as control. The cells were observed under the contrast phase microscope each day. After 48 h, cell proliferation was assayed by MTT method. The alkaline phasphatase (ALP) activities and calcium contents were measured after 3, 6, 9, and 12 days. The ALP positive colonies were histochemically stained after 10 days and the calcified nodules were stained by Alizarin Bordeaux after 12 days. Expressions of ALP, bone morphogenetic protein-2 (BMP-2) and Osterix (OSX) mRNA were measured at 0 h, 24 h, 48 h and 96 h. RESULTS: The cells exposed to the SEMFs were arranged in spiral appearance after 3 days. Compared with control, SEMFs inhibited cell proliferation (P < 0.01 or P < 0.05), but enhanced the maturation and mineralization of the osteoblasts. The results showed that SEMFs improved ALP activities, promoted calcium contents, increased calcified nodulues numbers, boosted expressions of ALP, BMP-2 and OSX mRNA. SEMFs with magnetic lines of force in parallel has stronger activities than those in vertical. CONCLUSION: The SEMFs at 1.8 mT and 50 Hz inhibit the proliferation of osteoblasts, but enhance the maturation and mineralization of osteoblasts.


Subject(s)
Cell Differentiation/radiation effects , Cell Proliferation/radiation effects , Electromagnetic Fields , Osteoblasts/cytology , Alkaline Phosphatase/genetics , Alkaline Phosphatase/metabolism , Animals , Animals, Newborn , Bone Morphogenetic Protein 2/genetics , Bone Morphogenetic Protein 2/metabolism , Cells, Cultured , RNA, Messenger/genetics , RNA, Messenger/metabolism , Rats , Rats, Sprague-Dawley , Skull/cytology , Transcription Factors/genetics , Transcription Factors/metabolism
2.
Zhong Yao Cai ; 35(1): 87-94, 2012 Jan.
Article in Chinese | MEDLINE | ID: mdl-22734418

ABSTRACT

OBJECTIVE: To study the protective effect of genistein on osteoblasts treated with hypoxia. METHODS: Rat osteoblasts were isolated from calvarias of newborn Sprague-Dawly rat by enzyme digestion and hypoxic environment was made by triple-gases incubator. Rat osteoblasts treated with hypoxia for 36 haurs. After 36 hours, cell viability, content of reactive oxygen species (ROS), analysis of cellular cycle and apoptosis, expression of proliferating cell nuclear antigen (PCNA), activity of iNOS and area of calcified nodules were detected. Total RNA was isolated and the gene expression of hypoxia inducible factor-1alpha (HIF-1alpha), BCL-2 and Caspase-3 was investigated by Real Time RT-PCR. RESULTS: Genistein could significantly improve cell viability, percentage of G1 phases, area of calcified nodules and decrease apoptosis rate, ROS content, expression of PCNA, activity of iNOS. Besides, mRNA levels of HIF-1alpha and BCL-2 were enhanced and that of Caspase-3 was inhibited. CONCLUSION: Genistein can protect osteoblasts from hypoxia and enhance osteogenic differentiation significantly.


Subject(s)
Apoptosis/drug effects , Genistein/pharmacology , Osteoblasts/drug effects , Proliferating Cell Nuclear Antigen/metabolism , Skull/cytology , Animals , Cell Cycle/drug effects , Cell Hypoxia , Cell Survival/drug effects , Cells, Cultured , Female , Hypoxia-Inducible Factor 1, alpha Subunit/genetics , Hypoxia-Inducible Factor 1, alpha Subunit/metabolism , Male , Osteoblasts/cytology , Osteoblasts/metabolism , RNA, Messenger/genetics , RNA, Messenger/metabolism , Rats , Rats, Sprague-Dawley , Reactive Oxygen Species/metabolism
3.
Yao Xue Xue Bao ; 47(2): 174-9, 2012 Feb.
Article in Chinese | MEDLINE | ID: mdl-22512027

ABSTRACT

This study is to investigate the effect of osthol on osteoclasts' activity, bone resorption as well as apoptosis in vitro, and explore the mechanism of osthol in preventing osteoporosis. Osteoclasts were separated from long-limb bones of new born rabbits, cultured in 24-well plate with glass slices and bone slices, and treated by 1 x 10(-5) mol x L(-1) osthol. Osteoclasts were identified by observing live cells with phase contrast microscope, HE staining, TRAP staining and toluidine blue staining of bone resorption pits. The numbers of bone resorption pits were counted as well as the surface area of bone resorption on bone slice. Osteoclasts were stained with acridine orange to detect the cell apoptosis. The ratio of apoptotic osteoclasts was observed under fluorescence microscope. The gene expression of RANKL, OPG, TRAP and p-JNK1/2 protein expression were examined using real time PCR and Western blotting, respectively. Comparing with the control group without osthol, the rates of apoptotic osteoclasts increased obviously and the number and area of bone resorption pits decreased evidently with 1 x 10(-5) mol x L(-1) osthol. There is significant difference between control group and experiment group treated by 1 x 10(-5) mol x L(-1) osthol. Therefore, the osthol through RANK+RANKL/TRAF6/Mkk/JNK signal pathway inhibits the osteoclasts activity, enhances osteoclasts apoptotic and inhibits the bone resorption.


Subject(s)
Apoptosis/drug effects , Bone Resorption , Coumarins/pharmacology , Osteoclasts/pathology , Acid Phosphatase/metabolism , Animals , Cells, Cultured , Cnidium/chemistry , Coumarins/isolation & purification , Gene Expression , Isoenzymes/metabolism , Mitogen-Activated Protein Kinase 8/metabolism , Mitogen-Activated Protein Kinase 9/metabolism , Osteoclasts/metabolism , Osteoprotegerin/metabolism , Phosphorylation , Plants, Medicinal/chemistry , RANK Ligand/metabolism , Rabbits , Seeds/chemistry , Signal Transduction , Tartrate-Resistant Acid Phosphatase
4.
Zhongguo Gu Shang ; 24(7): 589-93, 2011 Jul.
Article in Chinese | MEDLINE | ID: mdl-21870402

ABSTRACT

OBJECTIVE: To investigate the effect on early treatment with vacuum-assisted closure(VAC) to wound healing of acute explosion injury in pigs, and provide a new way for early treatment of battle wounds. METHODS: Eight healthy 3-month Landrace pigs of both sexes with the body mass of (50 +/- 5) kg were selected in the study. Sixteen battle wounds were made by explosion of same type detonator (pattern number: 660929F48840-55, included DDNP 0.3 g, RDX 0.7 g) in hibateral skin of buttock of 8 pigs, which were divided into experimental group and control group (pair wounds of left and right). The raw sufaces were thorough debrided at 3 h after exposure, according to the characteristics of treatment on the battlefield, experimental group was treated with VAC under the pressure of (-50 +/- 5) Kpa after debridement and sterilization and control group was treated with routine dry sterile gauze draping. Results of bacteriology (bacterial counts and the proportion of G+ bacteria) and pathology (HE stain and Masson stain) were detected at every wound before and after treatment. RESULTS: At the 3 days after treatment,the bacterial number in the experimental group was [(7.82 +/- 0.55) x 10(4) ] CFU/g, in control group was [(1.07 +/- 0.14) x 10(6)] CFU/g. There was significant difference between two groups. The proportion of G+ bacteria in experimental group was significantly increased. The raw surface in experimental group was clean with affluent and neoformative granulation tissue, blood vessels and collagen, necrotic tissue decreased obviously by pathological observation. CONCLUSION: VAC could reduce the quantity of bacteria, improve the proportion of G+ bacteria, and promote the formation of granulation tissue and the healing of wound. The VAC for the treatment of battle wounds has a positive effect.


Subject(s)
Explosions , Negative-Pressure Wound Therapy/methods , Soft Tissue Injuries/etiology , Soft Tissue Injuries/surgery , Animals , Colony Count, Microbial , Female , Male , Soft Tissue Injuries/microbiology , Soft Tissue Injuries/pathology , Staining and Labeling , Swine , Time Factors
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