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[Study on mercury in dental calculus].

It has been reported that dental calculus contains trace elements of mercury besides lead, cadmium and zinc. The mercury is one of the hazardous metal elements from the environmental point of view. The purpose of this study was to clarify the mechanism of the accumulation of mercury in the dental calculus. The results were as follows: 1. The concentration of mercury was 1.6 ppm in the dental calculus collected from the subjects with no amalgam fillings. 2. The most of the mercury was found in the organic fraction of the dental calculus. 3. In the culture study of Bacterionema matruchotii in vitro, with the increase of Bacterionema matruchotii the uptake of mercury by the bacteria increased. And the maximum uptake of mercury was seen between 7 to 14 days of the culture period. 4. After 7 days of culture, the bacterial cells were destroyed into several fractions and the quantity of the mercury in the respective fractions was assayed. About 90% of mercury was found in the cell wall. From these results, it was suggested that the uptake of mercury by the bacteria was the cause of mercury accumulation in the dental calculus.

Actinomycetaceae↗

High resolution electron microscopy of the interface between dental calculus and denture resin.

Dental calculus may grow on the denture surface. In order to demonstrate the mechanism of deposition, the interface between calculus and denture resin was investigated using a high resolution electron microscope. Ultrathin sections were also used for electron diffraction of selected areas to reveal any mineral phase. The mineral layers without mineralized bacteria adjacent to the denture surface revealed a marked variation in thickness and crystal shape. Three types of crystal shape were observed at the junction: needle-like, rod-like and plate-like crystals. High resolution electron microscopy (HREM) showed that both rod-like and plate-like crystals were an aggregation of fine crystallites. The lattice fringes of the fine crystallites were observed among the near atomic structures of resin polymer at the interface in all three types of crystals. The electron diffraction patterns of selected areas revealed that needle-like and rod-like crystals were composed of hydroxyapatite (OH-AP), while plate-like crystals were composed of a mixture of OH-AP and whitlockite. These findings indicate that, after saliva penetrates through the acrylic resin, calcium and phosphate ions in the saliva are trapped in the molecular chains of the resin polymer, while the local ion concentration then increases to reach supersaturation, whereas a spontaneous precipitation would occur at the superficial layer of the denture resin. Furthermore, a thin intermediate layer of crystallites might be indispensable for the scaffolding process in the calculus formation on the denture surface.

Acrylic Resins↗

Microbeam x-ray diffraction analysis of dental calculus.

The crystalline components of human dental calculus were investigated using microbeam x-ray diffraction analysis. Hydroxyapatite and octacalcium phosphate were most frequently found in that portion having porous and zonal structure. In the portion of the homogeneous illustration showing high calcification, whitlockite is a main component. Brushite was unexpectedly rare, and no calcite was detected in any portion of human dental calculus. The mechanism of the formation of dental calculus being considered in this paper is that octacalcium phosphate or brushite is formed during the initial stage of calcification of dental plaque, and is gradually hydrolyzed and transformed into hydroxyapatite and/or whitlockite.

Calcium Phosphates↗

Use of the feed additive sodium hexametaphosphate to prevent dental calculus in squirrel monkeys (Saimiri spp.).

Dental calculus and associated periodontal disease are serious clinical problems in captive squirrel monkeys. Calculus begins to appear as early as 2 years of age, with subsequent development of periodontal disease, dental abscessation, tooth loss and other sequelae. When used as a feed additive, sodium hexametaphosphate (HMP) retards the growth of calculus on previously cleaned teeth in rhesus monkeys, lemurs, and other species. We wanted to determine whether HMP would reduce dental calculus in squirrel monkeys (Saimiri spp.) whose teeth had not been pre-cleaned. The study animals were divided into two groups. One received a standard diet; the other received an identical diet containing the HMP additive at a concentration effective in other primate and non-primate species that had received dental cleaning prior to treatment with HMP. Teeth were graded for extent of calculus formation at the start of the study and at 3 and 6 months during HMP treatment. We compared the results from the two groups both by total score per animal and according to tooth type (e.g., incisors versus incisors in test and control groups). At the end of 6 months, dental calculus did not differ significantly between the experimental groups. Therefore, we conclude that HMP is ineffective in squirrel monkeys with preexisting dental calculus.

Animal Feed↗

Fluorescence spectroscopy of dental calculus.

BACKGROUND: Correct diagnosis of the presence and extent of subgingival calculus is important for periodontal treatment planning and reassessment after periodontal therapy. Traditional tactile methods often lack sensitivity. The present investigation shall contribute to understanding the fundamental fluorescence properties that may be useful for optical detection of both supra- and subgingival calculus. OBJECTIVES: The aim of this study was to investigate emission spectra from supra- and subgingival calculus under a wide range of excitation wavelengths. METHODS AND RESULTS: Extracted human molars with either supragingival or subgingival calculus deposits on the root surface were selected (n = 3 each). Emission spectra were recorded from the calculus of each tooth and corresponding areas of clean root surfaces using a fluorescence spectrophotometer at excitation wavelengths from 360 nm up to 580 nm in steps of 20 nm. The spectra were corrected for the wavelength dependent instrument sensitivity and normalized to peak intensity (the highest peak was set at 1.0). Emission spectra of calculus exhibited distinct fluorescence bands between 570 and 730 nm not present in clean root surfaces. This fluorescence emission was strongest for excitation wavelengths from 400 to 420 nm. No differences were observed between supra- and subgingival calculus. CONCLUSIONS: Human dental calculus can clearly be differentiated from clean root surfaces by emission spectrophotometry. The characteristic fluorescence emission of supra- and subgingival calculus may be due to a variety of porphyrin derivatives and may provide the basis for future diagnostic procedures.

Dental Calculus↗

Raman spectra of human dental calculus.

Raman spectra of human dental calculus have been observed for the first time by use of micro-Raman spectroscopy. The spectral features of calculus were influenced easily by heating caused by laser irradiation. Therefore, the measurements were carried out at relatively low power (5 mW, 1-micron spot size). The spectra could be characterized as phosphate vibrational bands due to the v1, v2, v3, and v4 modes. The overall spectral features did not resemble those of pure minerals such as brushite, octacalcium phosphate, and hydroxyapatite. There were spectral differences among mixed calculus particles obtained from 18 adults, probably due to variations in local mineral composition and differences among patients. However, the averaged spectral features did not vary significantly with formation period from 1 to 6 months. Freshly removed and stored (5-11 months) calculus also gave comparable Raman spectra. Measurements on a fractured sample indicated that Raman spectra at saliva and dentin interfaces are nearly identical, and major mineral constituents may not vary significantly along the growth axis of calculus.

Adult↗

Fluoride profiles in dental calculus from Japanese, Chinese and British residents.

Whether the fluoride concentrations and profiles differ in human dental calculus obtained from different countries was investigated. A total of 203 dental calculus deposits on 203 permanent teeth from residents (mean age, 52.1 years) of Nagoya (Japan), Shanghai (China), Leeds (Great Britain) and the Wuhan mountainous area (China, fluoridated area) were analysed. An abrasive microsampling procedure was used to examine fluoride distribution. There were five types of fluoride profiles in dental calculus in each area/country (designated types L, J, U, T, W). In supragingival calculus, type L (highest in the outermost layers) and type J (highest in the innermost layers) both had significantly higher values than type U (high in the surface and innermost layers) but were relatively identical. In subgingival calculus, type W (high in the outermost, mid and innermost layers) was characteristics. Calculus from the Wuhan mountainous area (fluoridated) had the highest fluoride concentration, followed by Leeds (non-fluoridated), and Nagoya and Shanghai (non-fluoridated) calculus had the lowest. Fluoride concentrations in supragingival calculus were higher in teeth extracted because of periodontal diseases than dental caries. It is concluded that fluoride concentrations and distribution in dental calculus differ from country to country, probably due to different fluoride environments.

Adult↗

Distribution of fluoride in human dental calculus.

The distribution of fluoride in human dental calculus was investigated using a mechanical sampling technique and the fluoride electrode. The fluoride concentrations were highest at the outer surface of dental calculus and, then fell to a plateau for the interior of the calculus, rising again as the tooth surface was approached. The coefficient of variation of fluoride concentration was significantly greater in the sub- than in the supragingival calculus (p < 0.01). The supragingival calculus thus tended to show a smoother distribution profile for fluoride than the subgingival calculus. Total fluoride, average fluoride, and maximum fluoride concentrations were not significantly different in supra- and subgingival calculus. No significant different were observed between males and females.

Adult↗

Purification of a protein component in extracts from supragingival dental calculus.

In the present study supragingival dental calculus of unknown age was collected from the mandibular incisors of three individuals and solubilized by EDTA. The extracts were examined by gel filtration, ionic exchange chromatography and amino acid analysis. A protein component with similar characteristics to the main protein component of the acquired enamel pellicle was a regular constituent of the calculus extracts from the three subjects.

Amino Acids↗

[The Ultradent apparatus for removing dental calculus].

New device for removal of dental calculus "Ultradent" is considered. Base functional units and their interaction are described. Technical specification of the device is reported. Serial production of the device was started from 1987.

Dental Calculus↗

A preliminary investigation into the ultrastructure of dental calculus and associated bacteria.

INTRODUCTION: Though dental calculus is generally recognised as comprising mineralised bacteria, areas of non-mineralised bacteria may be present. AIM: To investigate the ultrastructure of non-decalcified young and mature supragingival calculus and subgingival calculus, and the possible presence of internal viable bacteria. MATERIALS AND METHODS: Supragingival calculus was harvested from five patients, 9-10 weeks after scaling and root debridement. Five samples of mature supragingival and subgingival calculus were taken from patients presenting with adult periodontitis. Specimens were fixed and embedded for transmission electron microscopy. RESULTS: The ultrastructure of young and mature supragingival calculus was similar with various large and small crystal types. Non-mineralised channels were observed extending into the calculus, often joining extensive lacunae, both containing intact non-mineralised coccoid and rod-shaped microorganisms. Subgingival calculus possessed more uniform mineralisation without non-mineralised channels and lacunae. CONCLUSION: Supragingival calculus contains non-mineralised areas which contain bacteria and other debris. The viability of the bacteria, and their identification could not be determined in this preliminary investigation. As viable bacteria within these lacunae may provide a source of re-infection, further work needs to be done to identify the bacteria in the lacunae, and to determine their viability.

Adult↗

Dental calculus: recent insights into occurrence, formation, prevention, removal and oral health effects of supragingival and subgingival deposits.

Dental calculus, both supra- and subgingival occurs in the majority of adults worldwide. Dental calculus is calcified dental plaque, composed primarily of calcium phosphate mineral salts deposited between and within remnants of formerly viable microorganisms. A viable dental plaque covers mineralized calculus deposits. Levels of calculus and location of formation are population specific and are affected by oral hygiene habits, access to professional care, diet, age, ethnic origin, time since last dental cleaning, systemic disease and the use of prescription medications. In populations that practice regular oral hygiene and with access to regular professional care, supragingival dental calculus formation is restricted to tooth surfaces adjacent to the salivary ducts. Levels of supragingival calculus in these populations is minor and the calculus has little if any impact on oral-health. Subgingival calculus formation in these populations occurs coincident with periodontal disease (although the calculus itself appears to have little impact on attachment loss), the latter being correlated with dental plaque. In populations that do not practice regular hygiene and that do not have access to professional care, supragingival calculus occurs throughout the dentition and the extent of calculus formation can be extreme. In these populations, supragingival calculus is associated with the promotion of gingival recession. Subgingival calculus, in "low hygiene" populations, is extensive and is directly correlated with enhanced periodontal attachment loss. Despite extensive research, a complete understanding of the etiologic significance of subgingival calculus to periodontal disease remains elusive, due to inability to clearly differentiate effects of calculus versus "plaque on calculus". As a result, we are not entirely sure whether subgingival calculus is the cause or result of periodontal inflammation. Research suggests that subgingival calculus, at a minimum, may expand the radius of plaque induced periodontal injury. Removal of subgingival plaque and calculus remains the cornerstone of periodontal therapy. Calculus formation is the result of petrification of dental plaque biofilm, with mineral ions provided by bathing saliva or crevicular fluids. Supragingival calculus formation can be controlled by chemical mineralization inhibitors, applied in toothpastes or mouthrinses. These agents act to delay plaque calcification, keeping deposits in an amorphous non-hardened state to facilitate removal with regular hygiene. Clinical efficacy for these agents is typically assessed as the reduction in tartar area coverage on the teeth between dental cleaning. Research shows that topically applied mineralization inhibitors can also influence adhesion and hardness of calculus deposits on the tooth surface, facilitating removal. Future research in calculus may include the development of improved supragingival tartar control formulations, the development of treatments for the prevention of subgingival calculus formation, the development of improved methods for root detoxification and debridement and the development and application of sensitive diagnostic methods to assess subgingival debridement efficacy.

Adult↗

[Sex determination from dental calculus by polymerase chain reaction (PCR)].

We studied sex determination from dental calculus by the PCR method using primers which recognize DYZ3 region of Y-chromosome and DXZ1 of X-chromosome. The amounts of DNA obtained from 1.7-25.0 mg of dental calculus samples ranged 0.6-26.4 micrograms, and the majority of DNA was low molecular weight DNA. After PCR amplification, Y and X products were observed by the method of polyacrylamide gel electrophoresis. Both Y and X amplification products were observed in 26 out of 29 male samples, while, Y products was not detected in two samples and neither Y nor X product was detected in one sample. In 17 out of 20 female samples, only X product was observed, while, Y and X products were observed in three samples. The minimum amount of DNA for sex determination was 3 pg. Sex determination using DNA in dental calculus will be quite useful for forensic application because it can be done without destruction of morphological characteristics of teeth.

DNA↗

Aspirated dental calculus in a dog.

Aspiration of a dental calculus, with lodgement of the calculus in a mainstem bronchus, was identified in a dog after dental prophylaxis. The calculus was located by use of radiography and bronchoscopy, and was removed via thoracotomy. Aspiration is a possible complication of dental prophylaxis. Endotracheal intubation with a properly inflated cuff, and thoroughly rinsing the oral cavity after prophylaxis, may avoid this and similar complications.

Animals↗

Demonstration of the central dark line in crystals of dental calculus.

Using an electron microscope and Fourier transform infrared (FTIR) microspectroscopy, we studied the lattice images of crystallites of dental calculus to demonstrate the presence of the central dark line (CDL) in its crystallite and to compare this CDL with that of bone and synthetic hydroxyapatite crystals. Ultrastructural observations revealed clearly a number of crystallites, which displayed a proper lattice image and CDL similar to that of bone, in the dental calculus. FTIR microspectroscopy revealed that the dental calculus displayed a set of major spectra analogous to that of bone. These results suggest that the formation process of hydroxyapatite crystals with CDL in dental calculus, which is considered to be an unusual type of calcified structure in association with microorganisms, is basically similar to that of the ordinary calcifying hard tissues (bone, enamel, etc.).

Animals↗

Identification of calprotectin, a calcium binding leukocyte protein, in human dental calculus matrix.

Calprotectin is a calcium binding protein produced by leukocytes, macrophages and epithelial cells, and its levels in several tissues increase during infections and in many inflamed areas, suggesting that it may be an indicator of inflammatory activity. Osteopontin is a prominent phosphorylated glycoprotein in bone matrix, having calcium binding capacity. Recently, it has been reported that calprotectin and osteopontin are present in urinary stones (pathological mineralized masses in the body), and that these proteins may be involved in their formation. Dental calculus formed by mineralization of dental plaque is an inflammatory factor which may contribute to periodontal disease. It contains many organic components involved in mineralization. We recently found osteopontin molecules in human dental calculus and suggested that the components of its matrix may be similar to those of urinary stones. In this study, we investigated the presence of calprotectin in human dental calculus by immunohistochemical and immunoblotting analyses using a specific antibody for calprotectin. After fixation and demineralization of dental calculi adhered to tooth roots, sections embedded in paraffin were immunoreacted with the antibody for calprotectin and positive immunostaining for calprotectin was observed. Dental calculus proteins were then extracted with EDTA and separated by electrophoresis on 15% polyacrylamide gels. By immunoblotting analysis, 3 or 4 bands were observed at 11, 14.5, 22-25, 28 or 36.5 kDa and these patterns corresponded to those of calprotectin subunits. When non-immune rabbit serum was used instead of calprotectin-specific antibody as a negative control, no immunoreactivity was observed. These findings indicate that calprotectin is associated not only with antibacterial action but also with calcium binding capacity during dental calculus formation.

Calcium-Binding Proteins↗

Relationship between diet, dental calculus and periodontal disease in domestic and feral cats in Australia.

OBJECTIVE: To compare the dental calculus scores and prevalence of periodontal disease in domestic cats eating commercially available canned and dry foods with those in feral cats consuming a diet consisting of small mammals, birds, reptiles and insects. ANIMALS: Twenty-nine feral cats and 20 domestic cats were included in the study. PROCEDURE: A dental chart and dental calculus scores were recorded using the maxillary canine, maxillary third and fourth premolar, mandibular canine, mandibular fourth premolar and first molar teeth on both sides. Periodontal disease was recorded using gingival recession, increased periodontal pocket formation, radiographic alveolar bone loss, osteomyelitis, furcation and root exposure, and the presence of calculus as indicators. RESULTS: Dental calculus scores were significantly higher in domestic cats than in feral cats. There was no statistical difference in the prevalence of periodontal disease between the two groups. CONCLUSIONS: It can be inferred that diet may play a role in the accumulation of calculus, but a diet based on live prey does not protect cats against periodontal disease.

Animal Feed↗