EVALUATION OF APICAL DEVIATION IN ROOT CANALS INSTRUMENTED WITH K3 AND ProTaper SYSTEMS

Objectives:

this study evaluated the apical deviation of curved root canals instrumented with K3 and ProTaper systems.

Material and methods:

twenty root canals of human maxillary and mandibular first molars were employed, which were divided into 2 groups: group A (10 teeth) was instrumented with the K3 system, and group B (10 teeth) with the ProTaper system. Evaluation of deviation was performed by double radiographic exposure. Radiographs were achieved before and after instrumentation, with 0.3-second, thus allowing superimposition of images. Three-dimensional computerized tomograph was performed in 3 specimens in each group, as an additional means to evaluate the apical deviation.

Results:

were evaluated by the parametric test Student-Newman-Keuls at 5%, which did not reveal significance between groups concerning the apical deviation. The results of computerized tomograph images demonstrated that the larger deviation of the root canal occurred at the distolingual area for both systems.

Conclusions:

both techniques produced a mild apical deviation. Computerized microtomography was shown to be accurate for experimental endodontics studies.     

Epstein-Barr virus BMRF-2 and BDLF-3 expression in hairy leukoplakia

Hairy leukoplakia (HL) is a lesion found on the side of the tongue of immunocompromised individuals, including those with human immunodeficiency virus (HIV) infection. The lesion has unique histopathologic features and is characterised by high-level Epstein-Barr virus (EBV) replication, multiple EBV strains, and extensive inter-and intra-strain recombination. Expression of EBV genes spanning the entire viral life cycle from latency-associated genes to late, replicative genes has been detected in the lesion. HL thus provides a unique opportunity to study EBV expression in oral epithelium, and to study expression of novel EBV genes. We therefore constructed a cDNA library from an HL biopsy and detected expression of two genes not previously described in vivo: BMRF-2 and BDLF-3. Sequence analysis of the cDNAs revealed few amino acid changes from the B95-8 sequence. Expression of both genes was localized to the lower prickle cell layer of the tongue epithelium. BMRF-2 protein expression was primarily detected in the cell nuclei of the upper prickle cell layer. BDLF-3 protein expression was observed in the perinuclear space and Golgi compartment. The function of these proteins is currently under investigation.     

Gene expression analysis in cells of the dentine-pulp complex in healthy and carious teeth

Knowledge of the molecular events that occur in carious disease has so far been constrained due to difficulties in obtaining sufficient quantities of the dental tissues and cells involved. Our histological findings indicate that a pulp-odontoblast cellular complex can be obtained from carious and healthy human teeth when exposed to low-temperatures prior to pulpal extirpation and from rodent teeth processed at room-temperature. In contrast, pulpal tissue extracted from room-temperature processed human teeth and low-temperature processed rodent teeth resulted in the odontoblast layer remaining attached to the pulp chamber. Semi-quantitative RT-PCR (sq-RT-PCR) analysis confirmed that markers previously shown to be preferentially expressed in odontoblasts, namely dentin sialophosphoprotein (DSPP) and Nestin, amplified more readily from the extracted pulp-odontoblast complex, as compared to pulpal tissue alone, in both human and rodent samples. Subsequent gene expression analysis of collagen-1alpha and collagen-3alpha indicated levels were significantly higher in carious pulpal tissue. In addition, analysis characterising the expression of members of the transforming growth factor and bone morphogenic protein families and their receptors indicated in general, that these genes were expressed by healthy odontoblasts and up-regulated in both pulpal cells and odontoblasts in response to carious injury. Use of this temperature-sensitive dental tissue preparation procedure allows detection of differential gene expression in odontoblasts and other pulpal cells in healthy and carious tissue.     

The reduction of 2-bromomethyl-3-methyl- and 2,3-bis-bromomethyl-1,4-naphthoquinones,potential bioreductive alkylating agents. Electrochemical and computational studies

In the present work, 2,3-dimethyl-1,4-naphthoquinones, substituted at one or both side chains with bromine were prepared and submitted to electrochemical studies (cyclic voltammetry and electrolysis), in aprotic medium (DMF + 0.1 mol l^?1 TBAP), using different electrodes (Hg, GC and Au), to observe the role of bromide, as a good leaving group, in their electroreductions. The cyclic voltammograms are complex. Combined results from CV, chronoamperometry and analysis of the products of electrolysis, mainly dimers and the parent unsubstituted quinone, allowed the qualitative definition of the electrodic mechanism for the reduction of the brominated quinones. A reversible electronic transfer to the quinonoid group followed by the cleavage of C–Br, in an EC type mechanism, more specifically a reductive elimination, is suggested. The quinonoid radical is generated and suffers dimerization to electroactive dimers or a second electron uptake, furnishing the anion that can be protonated to yield 2,3-dimethyl-1,4-naphthoquinone, also electroactive. The additional waves are probably related to the reduction of quinomethide-derived products, upon comparison with a synthetic dimer. Computational studies corroborate the electrochemical observations. Despite the lack of unequivocal proof of quinonemethide generation, its intermediacy is highly probable and this has been proved to be essential for the biological activity of these compounds.     

Quantification of tooth wear: Conventional vs new method using toolmakers microscope and a three-dimensional measuring technique

Objectives

This study aimed to evaluate the reliability of a new CAD-CAM Laser scanning machine in detection of incisal tooth wear through a 6-month period and to compare the accuracy of using this new machine against measuring tooth wear using tool maker microscope and conventional tooth wear index.

Methods

Twenty participants (11 males and 9 females, mean age = 22.7 years, SD = 2.0) were assessed for incisal tooth wear of lower anterior teeth using Smith and Knight clinical tooth wear index (TWI) on two occasions, the study baseline and 6 months later. Stone dies for each tooth were prepared and scanned using the CAD-CAM Laser Cercon System (Cercon Smart Ceramics, DeguDent, Germany). Scanned images were printed and examined under a toolmaker microscope (Stedall-Dowding Machine Tool Company, Optique et Mecanique de Precision, Marcel Aubert SA, Switzerland) to quantify tooth wear and then the dies were directly assessed under the microscope to measure tooth wear. The Wilcoxon Signed Ranks Test was used to analyse the data.

Results

TWI scores for incisal edges were 0, 1, and 2 and were similar at both occasions. Scores 3 and 4 were not detected. Wear values measured by directly assessing the dies under the tool maker microscope (range = 517–656 μm, mean = 582 μm, and SD = 50) were significantly more than those measured from the Cercon digital machine images (range = 132–193 μm, mean  = 165 μm, and SD = 27) and both showed significant differences between the two occasions.

Conclusions

Measuring images obtained with Cercon digital machine under tool maker microscope allowed detection of wear progression over the 6-month period. However, measuring the dies of worn dentition directly under the tool maker microscope enabled detection of wear progression more accurately. Conventional method was the least sensitive for tooth wear quantification and was unable to identify wear progression in most cases.     

Involvement of angiotensin II type 1 receptors in interleukin-1β-induced interleukin-6 production in human gingival fibroblasts

The renin-angiotensin system is thought to be involved in inflammatory processes such as periodontitis. However, its precise role is still unclear. Therefore, in the present study the expression of the angiotensin II type 1 receptor (AT1R) was investigated in inflamed human gingival tissue, and the possible involvement of the AT1R in interleukin-1β (IL-1β)-induced interleukin-6 (IL-6) production by cultured human gingival fibroblasts (HGFs) was also studied. Immunohistochemical staining revealed that inflammatory cells and fibroblast-like cells were positive for the AT1R. However, in healthy gingival tissue, AT1R staining was very weak. The levels of AT1R mRNA and AT1R protein increased in HGFs after stimulation with IL-1β. The levels of IL-1β-induced IL6 mRNA and IL-6 protein were significantly reduced in AT1R gene-silenced HGFs compared with control HGFs. The data suggest that the AT1R may be involved in the regulation of gingival inflammation by modulating IL-1β-induced IL-6 production in HGFs.     

TGF-β1 gene polymorphism in renal transplant patients with and without gingival overgrowth

Oral Diseases (2011) 17 , 414–419 Background: The incidence of gingival overgrowth among renal transplant patients treated with cyclosporine A ranges from 13% to 84.6%, and the overgrowth is not only esthetic but also a medical problem. We studied the determination of association between TGF‐β1 (TGFB1) gene polymorphism and gingival overgrowth in kidney transplant patients medicated with cyclosporin A. Methods: Eighty‐four kidney transplant patients with gingival overgrowth and 140 control transplant patients without overgrowth were enrolled into the case control study. TGFB1 polymorphism was determined using the PCR‐RFLP assay for +869T>C in codon 10 and +915G>C in codon 25 as well as TaqMan real‐time PCR assays for promoter ?800G>A and ?509C>T SNPs. Results: In kidney transplant patients suffering from gingival overgrowth, mean score of gingival overgrowth was 1.38 ± 0.60, whereas in control subjects it was 0.0. The patients with gingival overgrowth were characterized by similar distribution of TGFB1 genotypes and allele in comparison to subjects without gingival overgrowth. Among 16 potentially possible haplotypes of TGFB1 gene, only four were observed in the studied sample of kidney transplant patients: G_C_T_G, G_T_C_G, G_C_C_C, and A_C_T_G, with similar frequency in patients with and without gingival overgrowth. Conclusion: No association between the TGFB1 gene polymorphism and gingival overgrowth was revealed in kidney transplant patients administered cyclosporine A.     

In vivo evaluation of an oral health toothpaste with 0.1% vitamin E acetate and 0.5% sunflower oil (with vitamin F)

Objectives : To measure the delivery of active ingredients of a new oral health toothpaste with zinc citrate trihydrate/triclosan and containing α‐tocopherol acetate (vitamin E) and sunflower oil (vitamin F) and compare its anti‐plaque/anti‐ginigvitis efficacy to that of a clinically proven control toothpaste. Methods : The new toothpaste contained 0.1% vitamin E acetate (α‐tocopherol acetate) and 0.5% sunflower oil as a source for vitamin F (linoleic acid). It also included an anti‐caries agent (0.32% sodium fluoride) and a proven gum‐health active system (0.3% triclosan and 0.75% zinc citrate trihydrate). Three studies were carried out. In study 1 (n=45) the bio‐availability of zinc and triclosan was measured in plaque 12h after brushing with the test toothpaste. In study 2 (n=93) the effect of the test toothpaste on plaque and gingival condition was investigated over three weeks in a randomised, parallel, double‐blind, controlled design. The control toothpaste was a fluoride toothpaste containing 0.3% triclosan. Healthy adult volunteers with GI>1.0 were enrolled and given a full mouth scale and polish. Plaque levels (Modified Quigley and Hein Index) and gingival condition (Gingival Index) were assessed at baseline and after three weeks. Study 3 (n=93) lasted for nine weeks. Subjects did not receive a full mouth scale and polish at baseline but the study was otherwise identical to study 2. Results : In study 1, no triclosan was detected in baseline plaque samples; mean triclosan concentration in plaque 12h after last brushing with the test toothpaste was 5.78μg/g (std=4.74); the mean zinc concentration rose from 15.2μg/g zinc ion in baseline plaque samples to 84.3μg/g zinc ion (p>0.0001) in samples taken 12h after brushing. In study 2, mean plaque and gingival indices were significantly reduced in both test and control group after three weeks compared to baseline; there was no significant difference between the test and control group after three weeks. In study 3, mean plaque and gingival indices were significantly reduced in both test and control group after three and nine weeks compared to baseline; there was no significant difference between the test and control group after three and nine weeks. Conclusion : The delivery of zinc and triclosan from a new oral health toothpaste containing zinc citrate trihydrate and triclosan was unaffected by the addition of α‐tocopherol acetate (vitamin E) and sunflower oil (vitamin F). The new toothpaste was effective in reducing plaque levels and improving gingival conditions to the same degree as a clinically proven positive control. Regular oral hygiene with this toothpaste is therefore beneficial for maintaining healthy and strong gums.     

模型转化法建立磨牙及其牙周组织的三维有限元模型

目的建立下颌第二恒磨牙及其牙周膜、牙槽骨的分析用模型。方法应用CAE软件3D MAX6.0及CATIA4.0生成磨牙及其牙周组织的三维有限元模型,利用HYPERMESH划分网格,生成可分析的三维有限元实体模型。结果建立了下颌第二恒磨牙及其牙周膜、牙槽骨的三维有限元模型,可以分别进行受力状态下应力、应变的分析。结论该模型可供口腔正畸矫治中磨牙的受力分析应用。