ABSTRACT
OBJECTIVES: This study aimed to evaluate and compare the impact of cigarette smoking (CS) and heated tobacco (HT) on the alteration of color and ultrastructural characteristics of human enamel and cementum. BACKGROUND: According to tobacco companies, a less harmful substitute for CS is HT products. Nevertheless, comprehensive research on the effects of HT on tooth structures has been lacking. This study aimed to evaluate and compare the impact of CS and HT on the alteration of color and ultrastructural characteristics of human enamel and cementum. MATERIALS AND METHODS: Thirty intact and noncarious human maxillary premolars extracted for orthodontic treatment purposes, previously disinfected, were used in the study. The specimens were randomly separated into six groups (n = 10), as follows: Group 1: enamel without smoking exposure; Group 2: enamel exposed to CS; Group 3: enamel exposed to HT; Group 4: cementum without smoking exposure; Group 5: cementum exposed to CS; and Group 6: cementum exposed to HT. The measurement of color change was conducted using a spectrophotometer. The surface alterations and mineral composition of enamel and cementum were evaluated using scanning electron microscopy and energy-dispersive X-ray spectroscopy. ANOVA test followed by Tukey's post hoc test was used to determine significant differences between groups. RESULTS: Results showed that CS had a more pronounced effect on enamel and cementum color changes than HT. The impact of CS and HT on color changes was more evident in cementum than in enamel. Surface morphology of enamel and cementum showed alterations in histology following exposure to both smoking types. Moreover, the mineral content experienced a significant reduction after using CS and HT. The reduction in calcium content after CS and HT exposure was similar. However, HT led to a significant decrease in the phosphorus content of enamel when compared with CS. At the same time, CS exposure in cementum resulted in a more significant reduction in Ca/P ratio than HT. CONCLUSIONS: Although HT may appear to present a lower danger to hard dental tissues than CS, it is not entirely harmless. CS results in more color changes on the enamel and cementum of teeth. Both smoking methods affected the mineral content of teeth, with CS having a significant effect on the roots, while HT significantly affected the crowns' mineral composition.
Subject(s)
Cigarette Smoking , Colorimetry , Dental Cementum , Dental Enamel , Microscopy, Electron, Scanning , Tobacco Products , Humans , Dental Cementum/pathology , Dental Cementum/chemistry , Dental Enamel/chemistry , Dental Enamel/drug effects , Tobacco Products/adverse effects , Colorimetry/methods , Cigarette Smoking/adverse effects , Hot Temperature/adverse effects , Spectrometry, X-Ray Emission , Bicuspid , ColorABSTRACT
In humans, the growth pattern of the acellular extrinsic fibre cementum (AEFC) has been useful to estimate the age-at-death. However, the structural organization behind such a pattern remains poorly understood. In this study tooth cementum from seven individuals from a Mexican modern skeletal series were analyzed with the aim of unveiling the AEFC collagenous and mineral structure using multimodal imaging approaches. The organization of collagen fibres was first determined using: light microscopy, transmission electron microscopy (TEM), electron tomography, and plasma FIB scanning electron microscopy (PFIB-SEM) tomography. The mineral properties were then investigated using: synchrotron small-angle X-ray scattering (SAXS) for T-parameter (correlation length between mineral particles); synchrotron X-ray diffraction (XRD) for L-parameter (mineral crystalline domain size estimation), alignment parameter (crystals preferred orientation) and lattice parameters a and c; as well as synchrotron X-ray fluorescence for spatial distribution of calcium, phosphorus and zinc. Results show that Sharpey's fibres branched out fibres that cover and uncover other collagen bundles forming aligned arched structures that are joined by these same fibres but in a parallel fashion. The parallel fibres are not set as a continuum on the same plane and when they are superimposed project the AEFC incremental lines due to the collagen birefringence. The orientation of the apatite crystallites is subject to the arrangement of the collagen fibres, and the obtained parameter values along with the elemental distribution maps, revealed this mineral tissue as relatively homogeneous. Therefore, no intrinsic characteristics of the mineral phase could be associated with the alternating AEFC incremental pattern.
Subject(s)
Dental Cementum , Minerals , X-Ray Diffraction , Humans , Dental Cementum/ultrastructure , Dental Cementum/chemistry , Dental Cementum/metabolism , X-Ray Diffraction/methods , Minerals/metabolism , Minerals/chemistry , Collagen/chemistry , Collagen/metabolism , Microscopy, Electron, Transmission/methods , Scattering, Small Angle , Microscopy, Electron, Scanning/methods , Electron Microscope Tomography/methods , Female , Adult , Male , Middle AgedABSTRACT
The cementum is a highly mineralized tissue that covers the tooth root. The regional differences among the types of cementum, especially in the extrinsic fibers that contribute to tooth support, remain controversial. Therefore, this study used second harmonic generation imaging in conjunction with automated collagen extraction and image analysis algorithms to facilitate the quantitative examination of the fiber characteristics and the changes occurring in these fibers over time. Acellular extrinsic fiber cementum (AEFC) was invariably observed in the superficial layer of the apical cementum in mouse molars, indicating that this region of the cementum plays a crucial role in supporting the tooth. The apical AEFC exhibited continuity and fiber characteristics comparable with the cervical AEFC, suggesting a common cellular origin for their formation. The cellular intrinsic fiber cementum present in the inner layer of the apical cementum showed consistent growth in the apical direction without layering. This study highlights the dynamic nature of the cementum in mouse molars and underscores the requirement for re-examining its structure and roles. The findings of the present study elucidate the morphophysiological features of cementum and have broader implications for the maintenance of periodontal tissue health.
Subject(s)
Collagen , Dental Cementum , Mice , Animals , Dental Cementum/chemistry , Collagen/analysis , Tooth Root/chemistry , Molar , Image Processing, Computer-Assisted , Periodontal Ligament/chemistryABSTRACT
Introduction: This study aimed to prepare a new root repair material including Portland cement, bismuth oxide, and nano-hydroxyapatite and analyze its physicochemical properties and its effects on the proliferation and differentiation of human dental pulp stem cells (hDPSCs). Material and Methods: Bismuth oxide as a radiopaque component and nano-hydroxyapatite particles were added to white Portland cement at 20% and 5% weight ratio, respectively. Characterization of the prepared cement was done using conventional methods. To examine the bioactivity of this new material, atomic absorption spectroscopy (AAS) was used for the investigation of the rate of calcium ions dissolution in simulated body fluid media. The viability of hDPSCs was assessed by an MTT assay after 1, 3 and 7 days. The odontogenic potential of this substance was evaluated by measuring alkaline phosphatase activity and alizarin red S staining. Results: Based on the bioactivity results, the cement presented high bio-activity, corroborating sufficiently with the calcium release patterns. The cell viability was significantly increased in new root repair material containing hydroxyapatite nanoparticles after 3 and 7 days (p<0.05). Conclusion: Moreover, alkaline phosphatase activity increased over 7 days in all experimental groups. The new cement containing nano-hydroxyapatite particles could be a good root repair material.
Objetivo: Este estudio tuvo como objetivo preparar un nuevo material de reparación de raíces que incluye cemento Portland, óxido de bismuto y nano-hidroxiapatita y analizar sus propiedades fisicoquímicas y sus efectos sobre la proliferación y diferenciación de células madre de pulpa dental humana. Material y Métodos: El óxido de bismuto como compo-nente radiopaco y las partículas de nano-hidroxiapatita se agregaron al cemento Portland blanco en una proporción en peso del 20 % y el 5 %, respectivamente. La caracterización del cemento preparado se realizó utilizando métodos con-vencionales. Para examinar la bioactividad de este nuevo material, se utilizó la espectroscopia de absorción atómica para investigar la velocidad de disolución de los iones de calcio en medio fluido corporal simulado. La viabilidad de las células madre de pulpa dental humana se evaluó mediante un ensayo MTT después de 1, 3 y 7 días. El potencial odontogénico de esta sustancia se evaluó midiendo la actividad de la fosfatasa alcalina y la tinción con rojo de alizarina S.Resultados: Con base en los resultados de bioactividad, el cemento presentó alta bioactividad, corroborando suficientemente con los patrones de liberación de calcio. La viabilidad celular aumentó significativamente en el nuevo material de reparación de raíces que contenía nanopartículas de hidroxiapatita después de 3 y 7 días (p<0,05). Conclusión: Además, la actividad de la fosfatasa alcalina aumentó durante 7 días en todos los grupos experimentales. El nuevo cemento que contiene partículas de nanohidroxiapatita podría ser un buen material de reparación radicular.
Subject(s)
Humans , Bismuthum Oxydatum , Silicates/chemical synthesis , Durapatite/chemical synthesis , Dental Cementum/chemistry , Root Canal Filling Materials , Stem Cells , Dental Pulp , NanoparticlesABSTRACT
El propósito de este estudio es evaluar la composición química de tres cementos: Portland tipo I (CEMEX Samper , Cundinamarca, Colombia), Portland tipo I (CEMEX-Diamante, Ibagué, Colombia) y ProRoot MTA (Dentsply-Maillefer, Ballaigues, Suiza). Se utilizó una muestra probabilística de 17 pastillas para cada tipo de cemento. El análisis se llevó a cabo con la microsonda EDAX (Mahwah, NJ, USA) del microscopio de barrido electrónico SEM FEI (Quanta 200, Hillsboro, Oregon USA), bajo condiciones estandarizadas de lectura de las muestras. Se hicieron cuatro lecturas por muestra, para un subtotal de 68 lecturas por cada tipo de cemento y un total de 208 lecturas. Los resultados se obtuvieron en porcentaje de peso sólido por elemento. Los datos generales fueron analizados por las pruebas ANOVA, comparaciones múltiples de Tukey y t de Student. Se observaron tres elementos comunes entre los tres cementos: Ca, Si y Al, pero se encontraron diferencias estadísticamente significativas de los elementos comunes entre el cemento ProRoot MTA y los cementos Portland I. El Bi solo se encontró en el ProRoot MTA y el S solo se encontró en los cementos Portland tipo I. Se concluye que la composición de los tres cementos es similar. Sin embargo, es necesario evaluar el impacto que puede tener, tanto la presencia de S en los cementos Portland I, como la diferencia de concentraciones de los elementos que fueron comunes en los tres cementos en cuanto a biocompatibilidad y efectividad clínica.
The objective of this study is to evaluate the chemical composition of three cements: Portland Type I (CEMEXSamper , Cundinamarca, Colombia), Portland Type I (CEMEX-Diamante, Ibague, Colombia) and Pro Root MTA (Dentsply-Maillefer, Ballaigues, Switzerland). A probabilistic sample of 17 tablets for each type of cement was used. The analysis was carried out with energy dispersive analysis with x-rays (EDAX) (Mahwah, NJ, USA) in the scanning electron microscope (SEM) FEI (Quanta 200, Hillsboro, Oregon, USA) under standard sample reading conditions. Four readings per sample were carried out for a total of 68 readings per cement, and a grand total of 208 readings. The results were obtained as a percentage of solid weight per element. General data was analyzed with the ANOVA test, and Tukey and t of Student multiple comparison tests. Three common elements were observed between the three cements: Ca, Si, and Al, but there were significant statistical differences between the common elements of the ProRoot MTA and the Portland cements I. The Bi was found only in the ProRoot MTA, and the S only in the Portland type I cements. It can be concluded then that the composition of the three cements is similar; however, it is necessary to evaluate the impact that the presence of S in the Portland I cements as well as the difference in concentrations of the three common elements may have in the biocompatibility and clinical effectiveness.
Subject(s)
Chemical Phenomena/methods , Dental Cementum/chemistry , Orthodontics , Root Canal Therapy , ColombiaABSTRACT
This study evaluated the attachment, chemo-attractive, proliferative and mineralization inductive potential of a bovine cementum extract (CPE) on newborn murine dental follicle cells (MDFC) in vitro. Cementum extract was partially purified by DEAE-cellulose chromatografy. A band representing and Mr of 55,000 was excised form the fel and the protein (s) were electroeluted. Attachment assays revealed that CPE (1.0 µg/ml) promoted MDFC attachment by 96 percent in comparison with collagen type I (5 µg/ml), and was five-fold greater compared with serum-free media (SFM), (p<0.05). Between 1 and 5 days CPE at 1.0 µg/ml and collagen type I at 5 µg/ml sustained more than 75 percent attachement and spreading of MDFC when compared to SFM (P<0.05). Contrary to other reports, fibronectin (0.5 µg/ml) was more potent than CPE in promoting MDFC chemoattraction (P<0.05). MDFC proliferation was stimulated by CPE (0.125 µg/ml), but this response was elicited only when CPE was used together with 10 percent FBS (37.3 percent) or 0.2 percent FBS (76 percent) (p<0.05). Alkaline phosphatase expression by MDFC was increased by CPE (1.0 µg/ml), in comparison to the control. Calcium deposits were detected by von Kossa staining in 14-day MDFC cultures treated with CPE. Nodule formation and its mineralization in long-term MDFC cultures were induced by CPE (1.0 µg/ml). Molecules(s) contained in CPE appear to regulate various biological activities in MDFC, indicating that CPE could play a key role in selecting progenitor cells required for the process of cementogenesis during development
Subject(s)
Animals , Cell Adhesion Molecules , Chemotaxis/drug effects , Dental Cementum/chemistry , Dental Sac/cytology , Dental Sac/drug effects , Cell Division , In Vitro Techniques , Proteins/pharmacology , Tissue Extracts/pharmacologySubject(s)
Humans , Male , Female , Infant, Newborn , Infant , Child, Preschool , Child , Dental Caries , Fluorine , Dental Cementum/chemistry , Tooth, Deciduous , Dentin/chemistry , Fluoride Poisoning , Fluorosis, Dental , Food Chemistry , Milk/chemistry , Osteoporosis , Dental Plaque/chemistry , Saliva/chemistrySubject(s)
Dental Cementum/chemistry , Dental Enamel/chemistry , Tooth Resorption/etiology , Tooth Resorption/pathology , Dental Arch/anatomy & histology , Dental Cementum/anatomy & histology , Dental Cementum/ultrastructure , Dental Enamel/anatomy & histology , Dental Enamel/ultrastructure , Endodontics , Microscopy, Electron, Scanning/methods , Microscopy , Tooth Cervix/anatomy & histology , Tooth Cervix/pathology , Tooth Cervix/ultrastructureABSTRACT
Se demostró la actividad antibacteriana "in vitro" frente a una cepa de S. mutans y a una de L. acidophillus, de cuatro materiales utilizados frecuentemente como medios de cementación temporal en la clínica odontológica. Estos materiales fueron dos a base de óxido de zinc eugenol (Temp-Bond y Provy) uno en base a óxido de zinc sin eugenol (Freegenol) y un cemento de protección pulpodentinaria a base de hidróxido de calcio (Dycal), el cual es utilizado frecuentemente en clínica como medio de cementación temporal. Se confeccionaron 60 probetas de cada material, las cuales se esterilizaron 15 minutos por cada lado con luz ultravioleta. Se colocaron 30 probetas de cada material en placas de cultivo con una cepa de S. mutans y 30 en placas con una cepa de L. acidophillus. El cultivo se hizo en Anaerobiosis (sistema jarra Gas-Pack) a 37 grados C, durante 72 horas. para el S. mutans. Para el L. acidophillus el cultivo se hizo en microaerofilia (sistema jarra con vela) a 37 grados C, y se controló a los 4 días. En una lupa cuenta colonias se midieron los diámetros de las áreas de inhibición del desarrollo bacteriano que se produjeron alrededor de las probetas; con estos datos se calculó mediante una fórmula las áreas de inhibición del desarrollo bacteriano que se produjeron alrededor de las probetas de los materiales. Para el estudio estadístico se utilizó el análisis de varianza de una vía, para un trabajo de diseño ortogonal y el test de Tuckey