OBJECTIVE: This study was conducted to examine the effect of vitrification on the survival and in vitro development of mice 1-cell zygotes. METHOD: Effects of exposure to vitrification solution and vitrification, with different concentrations of the cryoprotectant solution, were examined. The 1-cell zygotes were also subjected to a slow freezing- thawing method to compare with vitrification method. Solution composed of ethylene glycol (6.0 M, 5.0 M, 4.0 M) and sucrose (1.0 M) were used as cryopropectant. The experiments employed the method loading the embryos on electron microscope grids. RESULTS: I. The effects of exposure in vitrification solution 1-cell zygotes were non-toxic at all concentrations of the vitrification solution showing the survival rate between 88.1% and 97.5%. Development into 2-cell was more successful in the higher concentrations of the vitrification solution. Therefore, higher concentrations of the vitirification solution do not seem to cause any problems in vitrification procedure. II. The effects of vitrification method 1-cell zygotes showed the survival rate between 78.8% and 92.4%. The lowest and the highest survival rate was observed in the 6.0 M and 4.0 M vitrification solution, respectively. 2-cell development rates varied from 77.6% to 91.3%. Blastocyst development rate was shown highest in 5.0 M and the lowest in 4.0 M solution. Therefore, the highest 2-cell and blastocyst development rate was observed in 5.0 M solution. III. Comparison of vitrification and slow freezing-thawing method on 1-cell zygotes This experiment showed that 1-cell zygotes had the highest survival and development rates in 5.0 M vitrification solution. Vitrified group of 1-cell zygotes, in the 5.0 M vitrification solution, were compared with the group processed in slow freezing-thawing method. The development rate into 2-cell and blastocyst as well as the survival rate were higher in the vitrified group than in the slowly freezed group. CONCLUSION: 1. The results demonstrate that the best cryoprotectant is a 5.0 M vitrification solution for 1-cell zygotes. 2. Vitrification method significantly increases the survival rate of the 1-cell zygote and its development into 2-cell and blastocyst. Equilibration and exposure time during the vitrification was remarkerbly short in this experiment. Total time, from the exposure to vitirification solution to storage in the liquid nitrogen, was taken only 90 seconds. In contrast, the slow freezing-thawing method have taken more than four hours. Taken together, we presume that the overall time used for the procedure contributes to the results as an important parameter. 3. The loading of 1-cell zygotes on the EM grid is technically more simple and takes less time than the straw or cryo vial method.
Animals ; Blastocyst ; Embryonic Structures ; Ethylene Glycol ; Group Processes ; Mice ; Nitrogen ; Sucrose ; Survival Rate ; Vitrification* ; Zygote*

No abstract available.
Abscess* ; Citrobacter koseri

Secondary bone grafting in the alveolar cleft has proven effective in stabilizing the maxillary segments, providing continuity of the maxillary arch and facilitating the canine eruption into the proper position. The purpose of this study is to longitudinally evaluate the treatment results of secondary iliac bone grafting in 40 alveolar cleft patients with an observation period of more than 12 months. Interdental alveolar cleft height was measured in conventional dental radiographs taken no more than 1 month preoperatively, following the completion of all orthodontic expansion, using ratio of the adjacent tooth root and the narrowest point of cleft height. And then we measured the bone resorption rates in 1, 3, 6, and 12 postoperative months, respectively. There was significant positive correlation between presurgical alveolar cleft height and postoperative bone resorption rate. But there was not significant correlation between presurgical alveolar height and the age at operation. The overall success rate for achieving bony bridge across the cleft was 95%. The maximal bone resorption occured in 1 month after operation. In case that the secondary iliac bone graft was performed at the patient's pre-eruption stage of canine, 89% of the patient's canine erupted in 12 months after operation.
Bone Resorption ; Bone Transplantation* ; Humans ; Tooth Root ; Transplants

In order to investigate the potential cellular activity of remaind enamel epithelium of impacted tooth follicle, we have examined 75 tooth follicular tissues from impacted teeth by immunohistochemical methods. Particular focus on the proliferation, differentiation and apoptosis-antiapoptosis of remaind enamel epithelium was made. Follicular tissues were removed from impacted teeth, fixed in neutral formalin and prepared for 4micrometer thick 20 serial sections. Hematoxylin & eosin staining was done routinely, and the mucopolycharide materials of myxoid odontogenic mesenchyme was detected by histochemical reactions of toluidin blue, PAS, Van Gieson, Masson's trichrome Various antibodies, i.e., PCNA(proliferating cell nuclear antigen) and Ki-67 for proliferative activity, transglutaminase-C, transglutaminase-K, transglutaminase-E, TGF-beta1, bcl-2, and p53 were used. Apop-tag staining was also done to detect the phenomenon of apoptosis. Both of the reduced enamel epithelium in the luminal side of tooth follicle and the enamel epithelial rests scattered in the wall of tooth follicle showed frequent positive reaction for the PCNA and Ki-67, and these cells were also positive for the transglutaminase-C, K, E. On the other hand the enamel epithelium was not stained by Apop-tag staining but weakly positive for bcl-2 and p53. Relatively high amount of myxoid odontogenic mesenchyme was also diffusely observed in the tooth folliclular tissue, and the distribution of the myxoid odontogenic mesenchyme was closely related with the distribution of enamel epithelial rest infiltration. Taken together, these data may suggest that the remaind enamel epithelial cells are biologically acitive rather than the dormant state after the completion of tooth formation, and that the remaind enamel epithelium may has interaction with odontogenic mesenchyme and will not be degraded easily but may have a potential for the odontogenic tumors.
Antibodies ; Apoptosis ; Dental Enamel* ; Eosine Yellowish-(YS) ; Epithelial Cells ; Epithelium* ; Formaldehyde ; Hand ; Hematoxylin ; Humans* ; Mesoderm ; Odontogenic Tumors ; Phenobarbital ; Proliferating Cell Nuclear Antigen ; Tooth* ; Tooth, Impacted ; Transforming Growth Factor beta1

PURPOSE: To clinically determine the proportion of people with a fixed dissociating eye in patients with dissociated vertical deviation (DVD). METHODS: Medical records of 86 patients diagnosed with DVD in our department of ophthalmology from 2001 to November 2011 were retrospectively analyzed. RESULTS: Of the 71 patients, 25 (35.21%) showed a higher degree of dissociation in the fixating eye, 26 (36.62%) had higher dissociation in the non-fixating eye; 20 of 25 patients with a higher level of dissociation in the fixating eye and 22 of 26 patients with a higher level of dissociation in the non-fixating eye received surgical correction for DVD, such as superior rectus muscle recession or inferior oblique muscle anterior transposition. CONCLUSIONS: In DVD, the proportion of patients showing a higher level of dissociation in the fixating eye was significant. Patients with DVD require thorough evaluation; measurement of the level of dissociation and determination of the fixating eye is beneficial for management and surgical intervention.
Humans ; Medical Records ; Ophthalmology ; Retrospective Studies

Background: Most previous studies have evaluated flexion strength to assess recovery after arthroscopic rotator cuff (RC) repair.However, limited data are available regarding peak torque at the initial angle (iPT) because most studies have measured flexion strength for peak torque (PT), particularly in small- and medium-sized supraspinatus tears. The purpose of this study was to compare conventional PT and iPT to evaluate supraspinatus muscle strength after arthroscopic RC repair in patients with small- and medium-sized supraspinatus tears. Methods: Isokinetic muscle performance testing was performed in 42 patients with small tears and in 47 patients with medium-sized tears. PT and iPT were evaluated before and 1 year after surgery and were recorded at an angular velocity of 60°/sec and 180°/sec with an isokinetic test. Results: PT and iPT were significantly lower in the involved-side shoulders than in the uninvolved-side shoulders (PT: small tear, p < 0.001; medium tear, p < 0.001; iPT: small tear, p < 0.001; medium tear, p < 0.001) in both groups, preoperatively. However, postoperatively, in the involved-side shoulders, PTs were not different in both small- and medium-sized tears (all p > 0.05), but iPTs were significantly lower in the involved-side shoulders (small tear, p < 0.001; medium tear, p < 0.001). iPT was significantly lower in the involved side shoulders in the medium-sized tear group than in the small-sized tear group before and after surgery (p < 0.05). In the smalland medium-sized tear groups, tear size was significantly correlated with preoperative iPT in the involved-side shoulders (small tear: r = –0.304, p = 0.046; medium tear: r = –0.323, p= 0.027). However, pain visual analog scale was significantly correlated with preoperative (small tear: r = –0.455,p = 0.002; medium tear: r = –0.286, p = 0.044) and postoperative (small tear: r = –0.430, p = 0.005; medium tear: r = –0.354, p = 0.021) iPT in the involved-side shoulders. Furthermore, fatty infiltration grade of the supraspinatus muscle and global fatty degeneration index were not associated with preoperative and postoperative PT and iPT in each group (all p > 0.05). Conclusions iPT is as important as conventional PT in isokinetic testing to assess supraspinatus muscle strength before and after RC repair.

OBJECTIVES: The antimicrobial activity of silver nanoparticles has resulted in their widespread use in many consumer products. Yet, despite their many advantages, it is also important to determine whether silver nanoparticles may represent a hazard to the environment and human health. METHODS: Thus, to evaluate the genotoxic potential of silver nanoparticles, in vivo genotoxicity testing (OECD 474, in vivo micronuclei test) was conducted after exposing male and female Sprague-Dawley rats to silver nanoparticles by inhalation for 90 days according to OECD test guideline 413 (Subchronic Inhalation Toxicity: 90 Day Study) with a good laboratory practice system. The rats were exposed to silver nanoparticles (18 nm diameter) at concentrations of 0.7 x 10(6) particles/cm3 (low dose), 1.4 x 10(6) particles/cm3 (middle dose), and 2.9 x 10(6) particles/cm3 (high dose) for 6 hr/day in an inhalation chamber for 90 days. The rats were killed 24 hr after the last administration, then the femurs were removed and the bone marrow collected and evaluated for micronucleus induction. RESULTS: There were no statistically significant differences in the micronucleated polychromatic erythrocytes or in the ratio of polychromatic erythrocytes among the total erythrocytes after silver nanoparticle exposure when compared with the control. CONCLUSION: The present results suggest that exposure to silver nanoparticles by inhalation for 90 days does not induce genetic toxicity in male and female rat bone marrow in vivo.
Animals ; Bone Marrow ; Erythrocytes ; Female ; Femur ; Humans ; Inhalation ; Inhalation Exposure ; Male ; Mutagenicity Tests ; Nanoparticles ; Rats ; Rats, Sprague-Dawley ; Silver

Cerebral Infarction*

No abstract available.