Microscopic evaluation of bacterial colonization of interdental subgingival sites prior to and during experimental gingivitis in man.

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Variability of histologic criteria in clinically healthy human gingiva

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Comparison between histological and clinical parameters during human experimental gingivitis.

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In vivo early human dental plaque formation on different supporting substances. A scanning electron microscopic and bacteriological study.

Different studies have shown that various substances may have an influence on early human dental plaque formation. The purpose of the present study was to compare on tooth substances and supporting prosthetic materials the amount of plaque deposition by SEM and the quantity of selected bacteria using anaerobic culturing techniques. 5 bridges, replacing a missing molar or premolar, were incorporated in 3 patients. In the midbuccal area of each pontic, a semi-precision attachment was placed allowing the insertion of the following test facings: enamel, dentine, non gamma 2-amalgam, alloys of 85% and 55% gold, silver-palladium, chrome-cobalt, chrome-cobalt-titanium, and ceramic. For each material, 2 facings were fabricated. After 4 and 24 hours in situ, bacteriological samples were taken and processed for further identification. After a 2nd period of 4 and 24 hours in situ, the same facings were carefully removed and prepared for SEM-examination. All 4-hour specimens exhibited various areas covered by plaque, the amount of which varied with the different supporting substances. The very smooth surfaces (e.g., gold) harbored sparse deposits, while the rougher (e.g., amalgam) were covered by more plaque. After 24 hours of plaque development, an increase in the number of micro-organisms was noted for all the specimens. After 4 and 24 hours of plaque accumulation, no specific trends suggesting a preferential colonization on the different substances were observed. This study has shown that the amount of early deposits on different substances seems to be related to the degree of their surface roughness, while plaque formation was qualitatively similar.link_to_subscribed_fulltex

Histological and clinical parameters of human gingiva following 3 weeks of chemical (chlorhexidine) or mechanical plaque control

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Microvascular volumes in healthy and inflamed gingiva in humans.

It has been suggested that the vascular alterations found in inflamed gingiva may be of significance in the enhanced extension of the pathological process into the periodontium. The purpose of this investigation was to measured the changes in blood vascular volume occurring in gingiva with the onset of gingivitis and its resolution. Twenty-six individuals participated in this study. Gingival biopsies were taken following a 21-day experimental gingivitis, following resolution of a 21-d experimental gingivitis and during a 6-month experimental gingivitis and a 6-month period of optimal oral hygiene. A total of 126 biopsies was obtained, from which 378 sections were cut at 2 microns for stereological analysis. At low magnification, reference volumes were estimated using point counting procedures and expressed as mm3 of gingiva per mm length of vestibular gingiva, in a vestibulo-lingual plane. At higher magnification the ratio between the volume of vessels and connective tissue was calculated. The final results were expressed as mm3 of vessels per mm length of vestibular gingiva, in a vestibulo-lingual plane. The mean vessel volume expressed per unit length of vestibular gingiva ranged from 0.010 to 0.024 mm3/mm. No statistically significant differences in vascular volumes were found between inflamed and non-inflamed gingiva. It was concluded that the changes in vascular architecture during early gingivitis described in the literature had either taken place in the subjects prior to the time of experimentation or that any vascular changes (cytologic or functional) which had taken place may be compensatory for the changes in architecture described in the literature.link_to_subscribed_fulltex

Vascular adhesion molecules and initial development of inflammation in clinically healthy human keratinized mucosa around teeth and osseointegrated implants

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