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Biomedical subjects

O Fejerskov

Publications and source records attributed to O Fejerskov.

At least 163 records · Page 9Linked to original sources

Effect of long-term administration of fluoride on plasma fluoride and calcium in relation to forming enamel and dentin in rats.

Three groups of 1-month-old rats were kept on water containing 0.2, 56.5 and 113 parts/10(6) F-, respectively, for a period of 2 months. These groups were set up in order to study the relationship between long-term administration of high doses of waterborne fluoride, plasma values of fluoride and calcium and changes in forming dentin and enamel of the rat incisor. The microradiographic study revealed that increased levels of fluoride caused a delay in mineralization of the enamel. In the 113 parts/10(6) group the radiolucent areas in the enamel exhibited a distinct periodicity along the tooth, a phenomenon which cannot at present be explained. In the dentin the fluoride interfered with the process of mineralization giving rise to radiolucent and radiopaque banding in the experimental groups. With increasing levels of fluoride in the water supply a significant increase of plasma fluoride was recorded. In contrast the serum calcium values in both experimental groups were reduced to the same extent, which differed significantly from that of the control group. It is concluded that the fluoride doses which are needed to create fluorotic changes in rats may interfere with calcium metabolism and basic mineralization processes.

Amelogenesis↗

A scanning electron microscopic and microradiographic study of pits in fluorosed human enamel.

The aim of the present study has been to correlate the surface appearance of pitted, fluorosed enamel in the scanning electron microscope (SEM) with the microradiographic features of the underlying tissue. Intact enamel surfaces of severely fluorosed teeth appeared similar to that of normal enamel. In the unabraded surfaces discrete pits were sharply demarcated from the surrounding intact enamel surface leaving steep walls of parallel running rods. The microradiographic appearance of sections made through pits indicated that focal loss of surface enamel occurred corresponding to the inner highly hypomineralized part of the fluorotic subsurface lesion. The abrupt wall formation and the finding that the striae of Retzius never changed direction along the margins of the lesions indicated that pits in fluorosed enamel may be secondarily produced defects rather than true hypoplasias. Further evidence of the posteruptive origin of the defects was derived from the observation that enamel lamellae occasionally formed part of the lateral border. The relatively higher degree of radiopacity observed in the tissue surrounding the pit indicates a posteruptively acquired deposition of minerals in the exposed porous enamel.

Dental Enamel↗

Surface ultrastructure of some oral bacteria.

Adhesion of Streptococcus sanguis, Fusobacterium nucleatum and an Actinomyces sp. to enamel and epon and their interspecies cohesion was studied with scanning and transmission electron microscopy. For adhesion studies enamel or epon was coated with salivary macromolecules and then cells of S. sanguis and in some experiments also with F. nucleatum or Actinomyces sp. Cells of S. sanguis were seen scattered over the surface of a thin "pellicle" that was heavily stained, and F. nucleatum and Actinomyces sp. adhered to S. sanguis or directly to the "pellicle". For studies of cohesion S. sanguis was brought to cohere with F. nucleatum or Actinomyces sp. and then processed for transmission electron microscopy. The morphology of the cell surface structures involved was studied in negatively stained preparations or in thin sections of material treated with ruthenium red or poststained with uranyl and lead salts, phosphotungstic acid or periodic acid-thiocarbohydrazide-osmium tetroxide. S. sanguis demonstrated a fuzzy coat of fimbriae that seemed to unfold in areas of contact with other cells, while cells of F. nucleatum had 6-10 polar pilus-like fimbriae, which appeared to be instrumental in cohesion, as did a dense coat of long, slender fimbriae that covered cells of Actinomyces sp.

Actinomyces↗

Human dentition and experimental animals.

A review of the recent literature concerning enamel maturation patterns following cessation of protein matrix secretion confirms that developing rodent enamel exhibits an overall mineral distribution different from that of developing enamel in man, monkey, dog, and swine. This seems to be a result of structural differences of the enamel as the pattern of crystal growth appears similar in these species. Whether the differences in enamel structure are reflected in significant differences in cellular events leading to enamel formation and mineralization remain unknown, as detailed radioautographic and ultrastructural studies almost always have dealt with rodent teeth. It is therefore concluded that such studies should be initiated in experimental animals having an enamel formation and mineralization pattern strictly comparable to that of man. Some requirements for such an experimental animal are suggested.

Ameloblasts↗

Concanavalin A and ricinus communis receptor sites in normal human oral mucosa.

Fluorescein conjugates of concanavalin A (Con-A) and Ricinus communis fraction 120 (RCA120) were shown to bind to the cell surfaces of basal and spinous cell layers in oral buccal mucosa. Palatal epithelium showed distinct binding to basal and spinous cells; cell membranes in the granular layer occasionally bound Con-A and always RCA120. The ultrastructural localization of Con-A binding sites on exfoliated buccal cells was detected by the Con-A peroxidase staining method. The Con-A receptors were seen on the cell surface in association with the outer leaflet of the plasma membrane. The reaction products appeared as a homogeneous, electron-dense layer containing irregularly distributed globules.

Basement Membrane↗

Clinical appearance of dental fluorosis in permanent teeth in relation to histologic changes.

Based on studies in Northern Tanzania a new classification system of dental fluorosis is proposed. The classification system includes 10 scores designed to characterize the degree of dental fluorosis affecting buccal/lingual and occlusal surfaces. With aid of polarized and ordinary light microscopy the histologic features behind the individual scores are described. The macroscopic appearance of increasing degrees of dental fluorosis were well correlated to the degree of subsurface porosity. Above a certain level of subsurface hypomineralization various degrees of loss of surface enamel occurred, presumably as a result of posteruptively acquired injuries. Application of the new classification system to samples of children born in areas with 3.5, 6.0 and 21.0 parts/10(6) F- in the water supplies revealed that the distribution of dental fluorosis within the individual followed the same pattern irrespective of fluoride concentration in the water. While the classical Dean index was unable to distinguish between dental fluorosis in the 6.0 and the 21.0 parts/10(6) area it was possible with the new system to disclose that particularly the posterior teeth were significantly more affected in the latter area. Comparisons of degree of dental fluorosis with available measurements of enamel thickness proved that the within-tooth as well as within-dentition variations are determined by enamel thickness rather than length of exposure to body fluids. The limitations of the Dean index are discussed with special attention to its validity as a biological index in relation to current efforts to determine the minimal toxic effect of fluoride on the dental hard tissues.

Adolescent↗

Effect of experimental neutropenia on oral wound healing in guinea pigs.

The influence of experimental neutropenia on the wound healing process in standardized excisional palatal wounds was studied in 16 guinea pigs. Corresponding wounds in 15 normal animals were used as controls. Neutropenia was induced and maintained by daily injections of heterologous anti-neutrophil serum. One-micron sections from biopsies of palatal mucosa sampled 6, 24, 48 and 120 h after wounding were evaluated with special reference to the progress of epithelial wound repair and to the occurrence and location of inflammatory cells and bacteria. In animals treated with anti-serum, neutrophilic leukocytes disappeared from the wound cavity, whereas other inflammatory cells remained unchanged. Further bacterial invasion deep into the cavity was observed. The epithelial repair took place at a deeper level in the wounds of neutropenic animals compared with those of normal animals. The rate of re-epithelialization was the same in neutropenic and control wounds. The experiment indicates that the neutrophils in oral wounds provide a principal agency for host defense against microorganisms and probably thereby indirectly determine the direction and level of epithelial cell migration.

Agranulocytosis↗

Structural studies on calcium fluoride formation and uptake of fluoride in surface enamel in vitro.

The structural changes in human enamel during exposure to an acetate buffer, pH 4, containing 150 parts/10(6) fluoride have been studied using scanning electron microscopy and polarized light microscopy. After exposure for 2 h the enamel surface was covered by a fine-granular layer of calcium fluoride. The underlying enamel was highly eroded with an increased pore volume in the outer layer. Following an equilibration period of 3 months the uptake of fluoride in the apatite lattice had resulted in a highly mineralized, 100-micrometer-thick surface layer rich in fluoride covering a subsurface porous zone with an unchanged fluoride content. The deeply located, caries-like porous zone may have provided calcium and phosphate for saturation of the liquid.

Acetates↗

The permeability of a keratinizing squamous epithelium in culture.

Horseradish peroxidase or lanthanum was applied to the surface of keratinized oral epithelium growing in tissue culture and the extent of penetration of these substances examined with the electron microscope. Both tracer substances penetrated between the superficial keratinized squames of the tissue, the lanthanum reaching the basal cell layer and the peroxidase diffusing to within 3--8 cells of the basal layer. The permeability of the keratinized layer in this epithelium is in contrast to the situation in vivo where an intercellular barrier is found in the superficial layer. This difference might be related to the absence of membrane-coating granules from the tissue maintained in culture.

Animals↗