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1.
Nature ; 598(7882): 629-633, 2021 10.
Article in English | MEDLINE | ID: mdl-34526723

ABSTRACT

During the Early Bronze Age, populations of the western Eurasian steppe expanded across an immense area of northern Eurasia. Combined archaeological and genetic evidence supports widespread Early Bronze Age population movements out of the Pontic-Caspian steppe that resulted in gene flow across vast distances, linking populations of Yamnaya pastoralists in Scandinavia with pastoral populations (known as the Afanasievo) far to the east in the Altai Mountains1,2 and Mongolia3. Although some models hold that this expansion was the outcome of a newly mobile pastoral economy characterized by horse traction, bulk wagon transport4-6 and regular dietary dependence on meat and milk5, hard evidence for these economic features has not been found. Here we draw on proteomic analysis of dental calculus from individuals from the western Eurasian steppe to demonstrate a major transition in dairying at the start of the Bronze Age. The rapid onset of ubiquitous dairying at a point in time when steppe populations are known to have begun dispersing offers critical insight into a key catalyst of steppe mobility. The identification of horse milk proteins also indicates horse domestication by the Early Bronze Age, which provides support for its role in steppe dispersals. Our results point to a potential epicentre for horse domestication in the Pontic-Caspian steppe by the third millennium BC, and offer strong support for the notion that the novel exploitation of secondary animal products was a key driver of the expansions of Eurasian steppe pastoralists by the Early Bronze Age.


Subject(s)
Dairying/history , Human Migration , Proteome , Animals , Archaeology , Asia , Dental Calculus/metabolism , Domestication , Europe , Gene Flow , Grassland , History, Ancient , Horses , Humans , Milk
2.
Nat Commun ; 12(1): 632, 2021 01 27.
Article in English | MEDLINE | ID: mdl-33504791

ABSTRACT

Consuming the milk of other species is a unique adaptation of Homo sapiens, with implications for health, birth spacing and evolution. Key questions nonetheless remain regarding the origins of dairying and its relationship to the genetically-determined ability to drink milk into adulthood through lactase persistence (LP). As a major centre of LP diversity, Africa is of significant interest to the evolution of dairying. Here we report proteomic evidence for milk consumption in ancient Africa. Using liquid chromatography tandem mass spectrometry (LC-MS/MS) we identify dairy proteins in human dental calculus from northeastern Africa, directly demonstrating milk consumption at least six millennia ago. Our findings indicate that pastoralist groups were drinking milk as soon as herding spread into eastern Africa, at a time when the genetic adaptation for milk digestion was absent or rare. Our study links LP status in specific ancient individuals with direct evidence for their consumption of dairy products.


Subject(s)
Dairying , Feeding Behavior , Milk Proteins/metabolism , Africa, Eastern , Amino Acid Sequence , Animals , Archaeology , Bone and Bones/metabolism , Cattle , Collagen/metabolism , Dental Calculus/metabolism , Geography , Humans , Isotope Labeling , Lactase/metabolism , Lactoglobulins/chemistry , Milk Proteins/chemistry , Models, Molecular
3.
Colloids Surf B Biointerfaces ; 188: 110748, 2020 Apr.
Article in English | MEDLINE | ID: mdl-31884082

ABSTRACT

The cleaning and physicochemical properties on tooth root biointerfaces are pivotal for periodontal healing. Herein, this work investigated the impact of multi-treatment on the physicochemical features of tooth root surfaces and the responsive behavior of human gingival fibroblasts (hGFs). It was found that the combination of various mechanical treatments significantly affects the topographical pattern and size as well as wettability on tooth root surfaces. Furthermore, biological experiments revealed that hGF behaviors (i.e., cell adhesion, shape, spreading, arrangement, and viability) were regulated by the topography and wettability of tooth root surfaces. Also, there was no significant difference in the protein expression of NLRP3 inflammasome and IL-1ß in hGFs among tooth root surfaces under various treatments. This study provides new insights to efficiently remove the dental calculus and to understand the interaction between the tooth root interface and cell, which could guide the clinical operation and thereby is more conducive to periodontal recovery.


Subject(s)
Dental Calculus/metabolism , Tooth Root/metabolism , Cell Adhesion , Cell Survival , Dental Calculus/chemistry , Fibroblasts/cytology , Gingiva/cytology , Humans , Particle Size , Surface Properties , Tooth Root/chemistry , Wettability
4.
Biomed Res Int ; 2018: 8531961, 2018.
Article in English | MEDLINE | ID: mdl-29670909

ABSTRACT

Background/Purpose. Chronic periodontitis is an inflammatory disease of gums that causes loss of supporting structures of teeth, that is, gingiva, periodontal ligament, cementum, and alveolar bone. Levels of various cytokines in the serum, gingival tissues, and gingival crevicular fluid in patients with chronic periodontitis have been studied, but limited data are available on the level of cytokines in saliva. Therefore, a study was designed to determine levels of salivary IL-6 and IL-17 in patients with calculus associated chronic periodontitis. Materials and Methods. It was a comparative, cross-sectional study that is comprised of 41 healthy controls and 41 calculus associated chronic periodontitis patients (CP patients). According to the degree of attachment loss, CP patients were subcategorized as mild (CAL 1-2 mm), moderate (CAL 3-4 mm), and severe (CAL > 5 mm) forms of periodontitis. Salivary levels of IL-6 and IL-17 were determined using enzyme-linked immunosorbent assay (ELISA) technique. Data was analyzed using SPSS 20.0. Results. Between healthy controls and CP patients (moderate and severe disease), a statistically significant difference was observed in the concentrations of IL-6 and IL-17. In CP patients, the highest mean ± SD of salivary IL-6 and IL-17 was observed in severe CP, followed by moderate and mild CP. Regarding level of IL-6, a statistically significant difference was observed between mild and severe disease and between moderate and severe subcategories of CP patients. Similarly, statistically significant difference was observed in the level of IL-17 between mild and moderate, mild and severe disease, and moderate and severe disease. Conclusion. The levels of salivary IL-6 and IL-17 were increased significantly in calculus associated CP patients as compared to healthy controls and these levels increased with the progression of CP. Clinical Significance. Salivary levels of IL-6 and IL-17 may help in the subcategorization of CP.


Subject(s)
Chronic Periodontitis/complications , Chronic Periodontitis/metabolism , Dental Calculus/complications , Dental Calculus/metabolism , Interleukin-17/metabolism , Interleukin-6/metabolism , Saliva/chemistry , Severity of Illness Index , Adult , Case-Control Studies , Chronic Periodontitis/pathology , Dental Calculus/pathology , Female , Humans , Male
5.
BMC Oral Health ; 18(1): 52, 2018 03 27.
Article in English | MEDLINE | ID: mdl-29587817

ABSTRACT

BACKGROUND: Chlorhexidine gluconate (CHG) has been proven to be effective in preventing and controlling biofilm formation. At the same time, an increase in calculus formation is known as one of considerable side effects. The purpose of this study was to investigate whether mineral deposition preceding a calculus formation would occur at an early stage after the use of CHG using an in vitro saliva-related biofilm model. METHODS: Biofilms were developed on the MBEC™ device in brain heart infusion (BHI) broth containing 0.5% sucrose at 37 °C for 3 days under anaerobic conditions. Biofilms were periodically exposed to 1 min applications of 0.12% CHG every 12 h and incubated for up to 2 days in BHI containing a calcifying solution. Calcium and phosphate in the biofilm were measured using atomic absorption spectrophotometry and a phosphate assay kit, respectively. Morphological structure was observed using a scanning electron microscope (SEM), and chemical composition was analyzed with an electron probe microanalyzer (EPMA). RESULTS: The concentrations of Ca and Pi following a single exposure to CHG increased significantly compared with the control. Repeatedly exposing biofilms to CHG dose-dependently increased Ca deposition, and the amount of Ca was five times as much as that of the control. Pi levels in CHG-treated biofilms were significantly higher than those from the control group (p < 0.05); however, the influence of the number of exposures was limited. Analyses using an SEM and EPMA showed many clusters containing calcium and phosphate complexes in CHG-treated biofilms. Upon composition analysis of the clusters, calcium was detected at a greater concentration than phosphate. CONCLUSIONS: Findings suggested that CHG may promote mineral uptake into the biofilm soon after its use. It is necessary to disrupt the biofilm prior to the start of a CHG mouthwash in order to reduce the side effects associated with this procedure. The management of patients is also important.


Subject(s)
Chlorhexidine/analogs & derivatives , Dental Calculus/prevention & control , Biofilms/drug effects , Calcium/metabolism , Chlorhexidine/therapeutic use , Dental Calculus/metabolism , Dental Calculus/ultrastructure , Electron Probe Microanalysis , Humans , In Vitro Techniques , Microscopy, Electron, Scanning , Phosphates/metabolism , Saliva/drug effects , Spectrophotometry, Atomic
6.
J Neurol ; 265(6): 1334-1337, 2018 Jun.
Article in English | MEDLINE | ID: mdl-29600388

ABSTRACT

INTRODUCTION: In autopsy cases staged for sporadic Parkinson's disease (PD), the neuropathology is characterized by a preclinical phase that targets the enteric nervous system of the gastrointestinal tract (GIT). Therefore, the ENS might be a source of potential (presymptomatic) PD biomarkers. METHODS: In this clinically based study, we examined the alpha-synuclein (αSyn) concentration in an easily accessible protein storage medium of the GIT, dental calculus, in 21/50 patients with PD and 28/50 age- and gender-matched controls using ELISA. RESULTS: αSyn was detectable in dental calculus and the median concentration in the control patients was 8.6 pg/mg calculus (interquartile range 2.6-13.1 pg/mg). αSyn concentrations were significantly influenced by blood contamination and samples with a hemoglobin concentration of > 4000 ng/mL were excluded. There was no significant difference of αSyn concentrations in the dental calculus of PD patients (5.76 pg/mg, interquartile range 2.91-9.74 pg/mg) compared to those in controls (p = 0.40). CONCLUSION: The total αSyn concentration in dental calculus is not a suitable biomarker for sporadic PD. Disease-related variants such as oligomeric or phosphorylated αSyn in calculus might prove to be more specific.


Subject(s)
Dental Calculus/metabolism , Parkinson Disease/metabolism , alpha-Synuclein/metabolism , Aged , Biomarkers/metabolism , Dental Calculus/pathology , Enzyme-Linked Immunosorbent Assay , Female , Humans , Male , Middle Aged , Parkinson Disease/pathology
7.
Periodontol 2000 ; 76(1): 109-115, 2018 02.
Article in English | MEDLINE | ID: mdl-29194797

ABSTRACT

Dental calculus represents the first fossilized record of bacterial communities as a testimony of evolutionary biology. The development of dental calculus is a dynamic process that starts with a nonmineralized biofilm which eventually calcifies. Nonmineralized dental biofilm entraps particles from the oral cavity, including large amounts of oral bacteria, human proteins, viruses and food remnants, and preserves their DNA. The process of mineralization involves metabolic activities of the bacterial colonies and strengthens the attachment of nonmineralized biofilms to the tooth surface. From a clinical point of view, dental calculus always harbors a living, nonmineralized biofilm, jeopardizing the integrity of the dento-gingival or implanto-mucosal unit. This narrative review presents a brief historical overview of dental calculus formation and its clinical relevance in modern periodontal practice.


Subject(s)
Biofilms/growth & development , Dental Calculus/metabolism , Dental Calculus/microbiology , Disease Progression , Animals , Bacteria/metabolism , Biological Evolution , Calcification, Physiologic , Gingiva , Humans , Microbiota , Mouth/microbiology , Viruses
8.
Arch Oral Biol ; 70: 125-129, 2016 Oct.
Article in English | MEDLINE | ID: mdl-27348051

ABSTRACT

AIM: Matrix-Gla Protein (MGP) is one of the major Gla-containing protein associated with calcification process. It also has a high affinity for Ca2+ and hydroxyapatite. In this study we aimed to evaluate the MGP rs4236 [A/G] gene polymorphism in association with subgingival dental calculus. Also a possible relationship between MGP gene polymorphism and serum and GCF levels of MGP were examined. MATERIAL AND METHODS: MGP rs4236 [A/G] gene polymorphism was investigated in 110 patients with or without subgingival dental calculus, using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) techniques. Additionally, serum and GCF levels of MGP of the patients were compared according to subgingival dental calculus. RESULTS: Comparison of patients with and without subgingival dental calculus showed no statistically significant difference in MGP rs4236 [A/G] gene polymorphism (p=0.368). MGP concentrations in GCF of patients with subgingival dental calculus were statistically higher than those without subgingival dental calculus (p=0.032). However, a significant association was not observed between the genotypes of AA, AG and GG of the MGP rs4236 gene and the serum and GCF concentrations of MGP in subjects. CONCLUSION: In this study, it was found that MGP rs4236 [A/G] gene polymorphism was not to be associated with subgingival dental calculus. Also, that GCF MGP levels were detected higher in patients with subgingival dental calculus than those without subgingival dental calculus independently of polymorphism, may be the effect of adaptive mechanism to inhibit calculus formation.


Subject(s)
Calcium-Binding Proteins/genetics , Calcium-Binding Proteins/metabolism , Extracellular Matrix Proteins/genetics , Extracellular Matrix Proteins/metabolism , Gingival Crevicular Fluid/metabolism , Periodontal Diseases/metabolism , Adult , Calcium-Binding Proteins/blood , Dental Calculus/blood , Dental Calculus/genetics , Dental Calculus/metabolism , Extracellular Matrix Proteins/blood , Female , Genotype , Humans , Male , Middle Aged , Periodontal Diseases/blood , Periodontal Diseases/genetics , Polymerase Chain Reaction/methods , Polymorphism, Genetic , Polymorphism, Single Nucleotide , Tooth Calcification , Matrix Gla Protein
9.
Sci Rep ; 4: 7104, 2014 Nov 27.
Article in English | MEDLINE | ID: mdl-25429530

ABSTRACT

Milk is a major food of global economic importance, and its consumption is regarded as a classic example of gene-culture evolution. Humans have exploited animal milk as a food resource for at least 8500 years, but the origins, spread, and scale of dairying remain poorly understood. Indirect lines of evidence, such as lipid isotopic ratios of pottery residues, faunal mortality profiles, and lactase persistence allele frequencies, provide a partial picture of this process; however, in order to understand how, where, and when humans consumed milk products, it is necessary to link evidence of consumption directly to individuals and their dairy livestock. Here we report the first direct evidence of milk consumption, the whey protein ß-lactoglobulin (BLG), preserved in human dental calculus from the Bronze Age (ca. 3000 BCE) to the present day. Using protein tandem mass spectrometry, we demonstrate that BLG is a species-specific biomarker of dairy consumption, and we identify individuals consuming cattle, sheep, and goat milk products in the archaeological record. We then apply this method to human dental calculus from Greenland's medieval Norse colonies, and report a decline of this biomarker leading up to the abandonment of the Norse Greenland colonies in the 15(th) century CE.


Subject(s)
Dental Calculus/metabolism , Milk/metabolism , Animals , Archaeology , Biological Evolution , Cattle , Dairy Products , Humans , Lactoglobulins/metabolism , Sheep , Tandem Mass Spectrometry
10.
Transplantation ; 96(1): 102-7, 2013 Jul 15.
Article in English | MEDLINE | ID: mdl-23680932

ABSTRACT

BACKGROUND: Oral health and dental maintenance have become part of the standard of care for pediatric liver transplant recipients. These individuals tend to suffer particularly from dental problems, such as gingival enlargement, gingivitis, poor oral hygiene, dental hypoplasia, and caries. Saliva composition influences oral hygiene and disease states. We investigated saliva composition and its association with the oral health of young recipients of liver transplants. METHODS: In 70 patients, 36 liver transplant recipients (ages 2-23 years) and 34 healthy controls (ages 4-21 years), we measured the following variables: (a) oral hygiene, (b) gingival inflammation, (c) caries status, (d) dental calculus formation, (e) oral mucosal pH, and (f) salivary protein composition. RESULTS: Lower mean decayed, missing, and filled teeth index (P=0.0038), higher mean gingival index (P=0.0001), and higher mean calculus score (P=0.003) were found in the transplanted study group compared with the control. The mean mucosal pH for seven intraoral sites was higher in the transplant group (P=0.0006). The median salivary albumin concentration was significantly lower in the transplant group (P=0.01), as was the median salivary albumin/total protein ratio (P=0.0002). CONCLUSIONS: In post-liver transplant pediatric recipients, low incidence of caries, together with high incidence of dental calculus, could be attributed to elevated oral mucosal pH. Salivary albumin and immunoglobulin A levels were relatively low in these patients. Clinicians should pay particular attention to the oral health and dental care of liver transplanted children.


Subject(s)
Dental Calculus/diagnosis , Dental Caries/diagnosis , Gingivitis/diagnosis , Liver Transplantation , Mouth Mucosa/metabolism , Salvia/metabolism , Adolescent , Albumins/metabolism , Child , Child, Preschool , Cross-Sectional Studies , DMF Index , Dental Calculus/epidemiology , Dental Calculus/metabolism , Dental Caries/epidemiology , Dental Caries/metabolism , Female , Follow-Up Studies , Gingivitis/epidemiology , Gingivitis/metabolism , Humans , Hydrogen-Ion Concentration , Immunoglobulin A/metabolism , Incidence , Male , Oral Hygiene Index , Postoperative Complications/diagnosis , Postoperative Complications/metabolism , Young Adult
11.
Pediatr Nephrol ; 27(10): 1961-6, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22814946

ABSTRACT

BACKGROUND: This study aimed to determine whether dental calculus formation is really higher among patients with chronic kidney disease undergoing hemodialysis than among controls. Furthermore, the study evaluated correlations between dental calculus formation and dental plaque, variables that are related to renal disease and/or saliva composition. METHODS: The Renal Group was composed of 30 patients undergoing hemodialysis, whereas the Healthy Group had 30 clinically healthy patients. Stimulated whole saliva and parotid saliva were collected. Salivary flow rate and calcium and phosphate concentrations were determined. In the Renal Group the saliva collection was carried out before and after a hemodialysis session. Patients from both groups received intraoral exams, oral hygiene instructions, and dental scaling. Three months later, the dental calculus was measured by the Volpe-Manhold method to determine the rate of dental calculus formation. RESULTS: The Renal Group presented a higher rate of dental calculus formation (p < 0.01). Correlation was observed between rate of dental calculus formation and whole saliva flow rate in the Renal Group after a hemodialysis session (r = 0.44, p < 0.05). The presence of dental calculus was associated with phosphate concentration in whole saliva from the Renal Group (p < 0.05). CONCLUSION: In conclusion, patients undergoing hemodialysis presented accelerated dental calculus formation, probably due to salivary variables.


Subject(s)
Dental Calculus/etiology , Renal Dialysis/adverse effects , Renal Insufficiency, Chronic/therapy , Adolescent , Age Factors , Brazil , Case-Control Studies , Chi-Square Distribution , Child , Dental Calculus/metabolism , Dental Calculus/physiopathology , Female , Humans , Male , Phosphates/metabolism , Renal Insufficiency, Chronic/metabolism , Renal Insufficiency, Chronic/physiopathology , Risk Assessment , Risk Factors , Saliva/metabolism , Salivation , Time Factors , Young Adult
12.
Arch Oral Biol ; 56(10): 1106-11, 2011 Oct.
Article in English | MEDLINE | ID: mdl-21570059

ABSTRACT

BACKGROUND AND OBJECTIVE: High mobility group chromosomal protein B1 (HMGB1) and N2 (HMGN2), two members of high mobility group (HMG) family, play important role in inflammation. The purpose of this study was to investigate the expression of HMGB1 and HMGN2 in periodontistis. MATERIALS AND METHODS: The expression of HMGB1 and HMGN2 mRNA in gingival tissues and gingival crevicular fluid (GCF) in chronic periodontitis (CP), generalised aggressive periodontitis (G-AgP) patients and healthy subjects was detected by real-time PCR. The protein level of HMGB1 and HMGN2 in peri-implant crevicular fluid (PICF), peri-implant crevicular fluid of peri-implantitis (PI-PICF) and normal patients was determined by Western blotting. Furthermore, IL-1ß, IL-6, IL-8, TNF-α and HMGB1 levels in GCF, PI-PICF and healthy-PICF samples from different groups were determined by ELISA. RESULTS: HMGN2 expression was increased in inflamed gingival tissues and GCF from CP and G-ApG groups compared to control group. HMGB1 expression was the highest in the gingival tissues and GCF from CP patients and was accompanied by increased concentrations of IL-1ß, IL-6, IL-8 proinflammaory cytokines. CONCLUSION: To our knowledge, this is the first study reporting that the expression of HMGB1 and HMGN2 was increased in the gingival tissues and GCF in CP and G-AgP and the PICF in PICF. Our data suggest that HMGB1 may be a potential target for the therapy of periodontitis and PI.


Subject(s)
Dental Implants , Gingiva/metabolism , Gingival Crevicular Fluid/chemistry , HMGB1 Protein/analysis , HMGN2 Protein/analysis , Peri-Implantitis/metabolism , Periodontitis/metabolism , Adolescent , Adult , Aged , Aggressive Periodontitis/metabolism , Alveolar Bone Loss/metabolism , Chronic Periodontitis/metabolism , Dental Calculus/metabolism , Dental Plaque Index , Female , Gingival Hemorrhage/metabolism , Gingivitis/metabolism , Humans , Inflammation Mediators/analysis , Interleukin-1beta/analysis , Interleukin-6/analysis , Interleukin-8/analysis , Male , Middle Aged , Periodontal Pocket/metabolism , Periodontium/metabolism , Tumor Necrosis Factor-alpha/analysis , Young Adult
13.
J Periodontol ; 82(3): 445-51, 2011 Mar.
Article in English | MEDLINE | ID: mdl-20843234

ABSTRACT

BACKGROUND: A large amount of calculus may hamper the efficacy of daily oral hygiene and thereby accelerate plaque formation. Salivary concentrations of orthophosphate and pyrophosphate are important in preventing calculus formation. Activity of orthophosphate, pyrophosphate, and pyrophosphatase was studied in whole saliva in calculus-forming groups and plaque-forming groups. METHODS: The material for this study consists of 60 healthy individuals (age range: 15 to 30 years; mean age: 22 years). Depending on calculus index score, individuals were divided into four groups, each of 15 patients: Group 1, calculus index score 0 to 0.6; Group 2, calculus index score 0.7 to 1.8; Group 3, calculus index score 1.9 to 3; and Group 4, plaque group where index varied from 0 to 3. The saliva was collected and biochemically analyzed for concentration of orthophosphate, pyrophosphate, and pyrophosphatase. RESULTS: The mean values of orthophosphate in Groups 1, 2, 3, and 4 were 0.2559, 1.3639, 1.7311, and 0.1868 mM, respectively. The mean values of pyrophosphate in Groups 1, 2, 3, and 4 were 0.3258, 0.1091, 0.0314, and 0.3860 mM, respectively. The mean values of pyrophosphatase in Groups 1, 2, 3, and 4 were 10.7937, 15.4249, 27.2900, and 7.5427 units/ml, respectively. CONCLUSIONS: A holistic approach toward the control of periodontal disease should include antiplaque and anticalculus agents. The results are conclusive that the components orthophosphate, pyrophosphate, and pyrophosphatase present in saliva have a very significant role to play in formation and inhibition of calculus. This study reinforces the idea of using pyrophosphate and newer bisphosphonates as potential anticalculus agents.


Subject(s)
Dental Calculus/metabolism , Diphosphates/analysis , Phosphates/metabolism , Pyrophosphatases/metabolism , Adolescent , Adult , Dental Calculus/etiology , Dental Calculus/prevention & control , Dental Plaque/metabolism , Diphosphates/metabolism , Female , Humans , Male , Oral Hygiene Index , Phosphates/analysis , Pyrophosphatases/analysis , Saliva/chemistry , Young Adult
14.
Oral Dis ; 13(3): 296-302, 2007 May.
Article in English | MEDLINE | ID: mdl-17448212

ABSTRACT

OBJECTIVE: We studied the effects of food components on the in vitro formation of calcium phosphate precipitates. MATERIALS AND METHODS: The effects of food components, such as starch, soybean flour, fish meal, rapeseed oil, and coconut oil, on calcium phosphate precipitation were studied using a pH drop method. RESULTS: Although the addition of starch had no effect on the rate of precipitation of amorphous calcium phosphate (ACP), it increased both the rate of transformation of ACP to hydroxyapatite (HAP) and the induction time (i.e. time for the initiation of transformation of ACP to HAP to occur); this was irrespective of the heat treatment of the starch. Amylopectin (insoluble constituent of starch) was effective in increasing the rate of HAP transformation, but amylose (soluble constituent of starch) was not. Oil specimen obtained from rapeseed (400 microl ml(-1)) increased the entire reaction of calcium phosphate precipitation, but that from coconut did not. Protein food, such as soybean flour and fish meal, decreased the rate of transformation of ACP to HAP and increased the induction time, while they had no effect on the rate of ACP precipitation. CONCLUSION: These results suggest that carbohydrate and oil (both are staple diets for the humans) enhance oral calcification (dental calculus formation or re-mineralization of tooth enamel), while side dishes of protein food would decrease it.


Subject(s)
Dental Calculus/metabolism , Dietary Carbohydrates/metabolism , Dietary Fats/metabolism , Dietary Proteins/metabolism , Tooth Calcification/physiology , Calcium Phosphates/chemistry , Chemical Precipitation , Dietary Proteins/adverse effects , Fish Products/adverse effects , Hydrogen-Ion Concentration , Hydroxyapatites/metabolism , Plant Oils/metabolism , Glycine max/adverse effects , Glycine max/metabolism , Starch/metabolism , Tooth Remineralization
15.
Eur J Oral Sci ; 113(1): 20-7, 2005 Feb.
Article in English | MEDLINE | ID: mdl-15693825

ABSTRACT

The aims of this study were to evaluate (i): whether vitamin C in chewing gum, alone or in combination with carbamide, influences calculus formation, and (ii) whether carbamide affects the release, stability and uptake of vitamin C in a chewing gum. In two test series (Series I and II), 30 subjects, all calculus formers, participated. They were instructed to chew on five (Series I) or 10 (Series II) pieces of gum per day for a period of 3 months. The chewing gums were: vitamin C (60 mg, Series I), non-vitamin C (Series I) and vitamin C + carbamide (30 mg + 30 mg, Series II). In both series, no gum was used as a negative control. Calculus formation was scored on three lingual sites on the six anterior mandibular teeth according to the Volpe-Manhold index. The effect on plaque and gingivitis was also determined. A significant reduction in the total calculus score was observed after the use of vitamin C (33%) and vitamin C + carbamide (12%) gums compared with no gum use; this reduction was most pronounced in the heavy calculus formers. A reduced amount of visible plaque was also observed after use of vitamin C and non-vitamin C gum, but only the vitamin C gum reduced the number of bleeding sites (37%). In a separate study, the release, stability and uptake of vitamin C were evaluated using the iodine titration method in both saliva and urine after exposure to the following gums: vitamin C + carbamide (30 mg + 30 mg) and vitamin C (30 mg). There was no indication that carbamide affected the release, stability or uptake of vitamin C when used in a chewing gum.


Subject(s)
Ascorbic Acid/chemistry , Chewing Gum , Dental Calculus/prevention & control , Adult , Ascorbic Acid/administration & dosage , Cross-Over Studies , Cuspid/pathology , Dental Calculus/metabolism , Dental Calculus/pathology , Dental Plaque/prevention & control , Diffusion , Double-Blind Method , Drug Combinations , Drug Stability , Female , Gingivitis/prevention & control , Humans , Incisor/pathology , Iodine/analysis , Iodine/urine , Male , Mandible , Middle Aged , Saliva/chemistry , Saliva/drug effects , Saliva/metabolism , Urea/administration & dosage , Urea/chemistry
17.
Crit Rev Oral Biol Med ; 13(5): 426-41, 2002.
Article in English | MEDLINE | ID: mdl-12393761

ABSTRACT

Dental calculus is composed of inorganic components and organic matrix. Brushite, dicalcium phosphate dihydrate, octacalcium phosphate, hydroxyapatite, and whitlockite form the mineral part of dental calculus. Salivary proteins selectively adsorb on the tooth surface to form an acquired pellicle. It is followed by the adherence of various oral micro-organisms. Fimbriae, flagella, and some other surface proteins are essential for microbial adherence. Microbial co-aggregation and co-adhesion enable some micro-organisms, which are incapable of adhering, to adhere to the pellicle-coated tooth surface. Once organisms attach to the tooth surface, new genes could be expressed so that mature dental plaque can form and biofilm bacteria assume increased resistance to antimicrobial agents. Supersaturation of saliva and plaque fluid with respect to calcium phosphates is the driving force for plaque mineralization. Both salivary flow rate and plaque pH appear to influence the saturation degree of calcium phosphates. Acidic phospholipids and specific proteolipids present in cell membranes play a key role in microbial mineralization. The roles of crystal growth inhibitors, promoters, and organic acids in calculus formation are discussed. Application of biofilm culture systems in plaque mineralization is concisely reviewed. Anti-calculus agents used--centering on triclosan plus polyvinyl methyl ether/maleic acid copolymer, pyrophosphate plus polyvinyl methyl ether/maleic acid copolymer, and zinc ion-in commercial dentifrices are also discussed in this paper.


Subject(s)
Dental Calculus/etiology , Dental Calculus/prevention & control , Bacterial Adhesion , Biofilms/growth & development , Calcium Phosphates/metabolism , Dental Calculus/chemistry , Dental Calculus/metabolism , Dental Pellicle , Dental Plaque/metabolism , Dentifrices/therapeutic use , Diphosphates/therapeutic use , Humans , Maleates/therapeutic use , Polyethylenes/therapeutic use , Salivary Proteins and Peptides/physiology , Triclosan/therapeutic use , Zinc Compounds/therapeutic use
18.
J Synchrotron Radiat ; 8(Pt 2): 990-2, 2001 Mar 01.
Article in English | MEDLINE | ID: mdl-11513004

ABSTRACT

We present here the first study of the local environment of zinc ions in biological calcium phosphates. It was suggested from in vitro studies that zinc inhibits the formation of hydroxyapatite and promotes the formation of more soluble phases, like tricalcium phosphate. Several mechanisms of zinc - calcium phosphate interaction were proposed, yielding either to the adsorption or to the incorporation of zinc ions into the phosphate structure. The results obtained here show that, under in vivo conditions, the zinc atoms are fully incorporated into the crystalline structure of the calcium phosphates.


Subject(s)
Dental Calculus/chemistry , Zinc/chemistry , Calcium Phosphates/chemistry , Calcium Phosphates/metabolism , Dental Calculus/metabolism , Fourier Analysis , Humans , Spectrometry, X-Ray Emission/methods , Zinc/metabolism
19.
N Z Dent J ; 97(427): 9-14, 2001 Mar.
Article in English | MEDLINE | ID: mdl-11355249

ABSTRACT

Several individual species of dental plaque bacteria have the ability to initiate the precipitation of calcium phosphate minerals in vitro; other plaque components have been shown to inhibit mineralisation. We have examined subjects' overall plaque mineralisation promoter and inhibitor properties, and have attempted to correlate them with supragingival calculus development over 6 months. Three-day-old plaque was collected from 22 adult subjects at the start and end of the study. To detect promoter activity, the plaque was placed in a suspension of brushite, the liquid phase of which was supersaturated with respect to hydroxyapatite. The extent of mineralisation was determined by the rise in phosphate concentration over 4 days. To detect inhibitor activity, plaque was placed in a similar suspension, which also contained hydroxyapatite. Promoter activity was compared with that hydroxyapatite, and inhibitor activity was compared with polyaspartate. The subjects' teeth were scaled at the start of the study, and calculus deposition was measured at the end using the Volpe Manhold method. Most plaque samples showed some promoter or inhibitor activity, or both, but no significant correlation existed between these activities and a subject's development of calculus. A significant inverse correlation existed between plaque mineralisation promoter activity and its inhibitor activity at the start of the study. Our results suggest that the nucleating and mineralisation inhibitory properties of young plaque will probably not be a useful target for a practical preventive methodology for supragingival calculus.


Subject(s)
Calcium Phosphates/metabolism , Dental Calculus/metabolism , Dental Plaque/metabolism , Adult , Aged , Calcium Phosphates/agonists , Calcium Phosphates/antagonists & inhibitors , Crystallization , Dental Calculus/chemistry , Dental Calculus/etiology , Dental Plaque/chemistry , Dental Plaque/complications , Depression, Chemical , Female , Humans , Hydroxyapatites/metabolism , Male , Middle Aged , Statistics, Nonparametric , Stimulation, Chemical
20.
Postepy Hig Med Dosw ; 55(5): 733-54, 2001.
Article in Polish | MEDLINE | ID: mdl-11795206

ABSTRACT

To non mucin proteins of human saliva belong: cystatins, statherin, histatins and acidic proline-rich protein. These saliva proteins influence hard and soft tissues by forming a pellicle layer on oral mucosa and enamel, by taking part in removing bacteria or initiating of bacterial colonization. Most of them are able to inhibit the formation of dental calculus and control the calcium phosphate homeostasis.


Subject(s)
Dental Calculus/metabolism , Saliva/chemistry , Saliva/physiology , Salivary Proteins and Peptides/chemistry , Salivary Proteins and Peptides/physiology , Bacterial Adhesion , Calcium Phosphates/chemistry , Cystatins/chemistry , Cystatins/physiology , Dental Calculus/prevention & control , Dental Pellicle , Humans , Peptides/chemistry , Peptides/physiology , Proline-Rich Protein Domains , Proteins/chemistry , Proteins/physiology
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