ABSTRACT
BACKGROUND:Nanosized cell-type tissue-engineered bone is a good scaffold material possessing the merits of stem cells and nanomaterials to fabricate bone and soft tissue formation. OBJECTIVE:To explore the method of constructing nano-sized cell-type tissue-engineered bone and to explore its application in the repair of mandibular bone defects. METHODS:One New Zealand white rabbit was taken to isolate bone marrow stromal stem cells by centrifugation. Then, the cells were induced to differentiate into osteoblasts. Osteoblasts (3×108/L, 10 μL) were inoculated into the prepared nano-phase hydroxyapatite/collagen composite to produce the nano-sized cell-type tissue-engineered bone. Another 20 New Zealand white rabbits were taken to make a unilateral puncture-type bone defect model of 15 mm×8 mm. These model rabbits were thereafter randomized into control and artificial bone groups (n=10 per group), followed by no intervention and implantation of nano-sized cell-type tissue-engineered bone, respectively. Repair effects were compared between the two groups. RESULTS AND CONCLUSION:(1) Under the inverted microscope, osteoblasts grew along the material in each group, and the number of cells increased with the prolongation of the culture time. (2) Under the scanning electron microscope, a large number of spindle- or polygon-shaped adherent cells grew well on the surface of the tissue-engineered bone. (3) The defect in the artificial bone group was lessened at 4 weeks after implantation and disappeared at 8 weeks after implantation, and there was no clear boundary with the surrounding tissue. In the control group, the defect size changed little at 4 weeks and reduced at 8 weeks after implantation, and a clear boundary with the surrounding tissue was observed. (4) Bone density, trabecular thickness and trabecular number were significantly higher in the artificial bone group than the control group at 4 and 8 weeks after implantation (P < 0.05). (5) At 4 weeks after implantation, many new bones at the defect site were detected in the artificial bone group, and a large number of mature bone cells were visible at 8 weeks. In the control group, a few osteoblasts were found at the defect site with low bone maturation at 4 and 8 weeks after implantation. These findings suggest that the implantation of nanosized cell-type tissue-engineered bone into the defect site can considerably promote defect healing and achieve ideal repair effects.
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the effect of periodontal infection on circulating C-reactive protein (CRP) in type 2 diabetes patients.</p><p><b>METHODS</b>32 diabetes patients with advanced periodontitis participated in this study. They were compared to a group of 32 diabetes patients without periodontal disease, who were mathed with regard to age (+/- 3 years), gender and body mass index (+/- 1 kg/m2). The concentration of CRP on circulation was measured by ELISA.</p><p><b>RESULTS</b>Significant difference was found in the level of CRP and the percentage of subjects with elevated CRP levels > or = 3 mg/L on circulation between the two groups(P < 0.05).</p><p><b>CONCLUSION</b>Periodontal infection results in higher circulating CRP in type 2 diabetes patients. This elevated inflammatory factor may exacerbate insulin resistance and increase the risk for great vessels complications of diabetes mellitus.</p>
Subject(s)
Adult , Female , Humans , Male , Middle Aged , C-Reactive Protein , Diabetes Mellitus, Type 2 , Periodontal Attachment Loss , Periodontal Pocket , PeriodontitisABSTRACT
<p><b>OBJECTIVE</b>To investigate the induction of apoptosis on human oral epidermoid carcinoma KB cells and multidrug resistant KBv200 cells by Matrine.</p><p><b>METHODS</b>MTT assay was used to investigate the inhibition ability of Matrine on the cells in vitro. Transmission electron microscope was used to observe the ultrastructure feature of cells. after treated by Matrine. Acridine orange (AO)/Ethidium bromide (EB) fluorescent staining and flow cytometry were used to observe apoptosis induced by Matrine. Flow cytometry was applied to study the effects of the drug on cell cycles of the cells.</p><p><b>RESULTS</b>When 0.50, 1.00, 1.50, 2.00 mg/ml of Matrine was used, the vital rates of KB and KBv200 cells were decreased according to Matrine's concentration. The IC50 concentrations of Matrine on KB and KBv200 cells were 1.35 mg/ml and 1.43 mg/ml individually. The results of AO/EB fluorescent staining and flow cytometry showed that Matrine could induce apoptosis of two kinds of cells. While observed by transmission electron microscope, there were more contraction of cells, condensation of nuclei, bubble of cytoplasm in both kinds of cells after treated by Matrine. Matrine could stop the growth of KB and KBv200 cells at S period and restrain mitosis of cells.</p><p><b>CONCLUSION</b>Matrine can inhibit the growth of KB and KBv200 cells by inducing apoptosis. The apoptosis effect is dose-dependent and it has certain relation to the blocking of S period cells.</p>
Subject(s)
Humans , Alkaloids , Apoptosis , Carcinoma, Squamous Cell , KB Cells , QuinolizinesABSTRACT
Objective To investigate the clinical characteristics of septicemia in type 2 diabetes mellitus,to enhance prevention level and decrease death rate.Methods A retrospective study was carried out,the data were collected from 58 cases of type 2 diabetes mellitus complicated by septicemia in our hospital in the past 13 years.Results The pathogenic invasive pathways included:19 cases of urinary tract,17 cases of respiratory tract,7 cases of intravenous catheter detain,7 cases of biliary tract,1 case of skin breakage,and 7 cases of unclear origin.Twenty-three of 58 cases were from nosoeomial infection (39.7%),among which 10 cases of urethral detain,7 cases of intravenous catheter detain,and 6 cases of respiratory tract infection.Pathogenic distribution was as following:24 cases of klehsiella pneumoniae,16 cases of escherichia coli,10 cases of staph aureus,2 cases of staphylococcus cohnii cohnii,2 cases of staphylococcus epidermidis,2 cases of pseudomonas putida,2 cases of candida glabrata.Among the 24 cases of llehsiella pneumoniae,12 cases showed migrating hepatapostema (50.0%),and 15 showed pneumatosis phenomenon in the intrahepatie bile (62.5%).Two cases originated from fungal septicemia.Among 56 cases under antibacterial therapy 15 cases developed fungal septicemia (26.8%).Fifty-eight cases were treated with insulin for forcing down serum glucose,56 cases of bacterial septicemia were treated with the third generation cephalosporins and fluoroquinolones.Two cases of pseudomonas putida septicemia were treated with intravenous injection of fluconazole.Seven cases died (12.1%).Conclusions Gram-negative bacilli were the major pathogens of septicemia in type 2 diabetes mellitus.Migrating hepatapostema and pneumatosis phenomenon in the intrahepatic bile often showed klebsiella pneumoniae septicemia.The important risk factors for septicemia were intravenous catheter detain and urethral detain.Therefore,strictly aseptic operation and removing vessel detain in time is very important.It is key points to make an early diagnosis,have a strong antibiosis therapy and treat the migrating pathogenic focus.And it is important to intensify serum glucose monitoring and strengthen supportive treatment.