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Biomedical subjects

E Hausmann

Publications and source records attributed to E Hausmann.

At least 91 records · Page 5Linked to original sources

Experimental alveolar bone loss in the monkey evaluated by 125I absorptiometry.

An 125I absorptiometry technique is described which has sufficient precision to detect the alveolar bone loss associated with ligature-related periodontitis in the monkey. Six monkeys had significant drops in alveolar bone mass 14 days after the the application of a silk ligature around the gingival margin of an adjacent tooth. Variation in the magnitude of bone loss was observed. These may represent variations in the pathogenicity of the microflora produced in response to a ligature and/or variation in host response to the insult produced by specific dental plaque organisms. The lack of bone loss post-ligature plus antibiotic therapy supports the theory that the bacterial-host interaction, not simply irritation from the ligature alone, is responsible for the bone loss. The potential for bone regeneration after ligature-induced bone loss is demonstrated.

Absorption↗

Longitudinal study of experimentally induced periodontal disease in Macaca arctoides: relationship between microflora and alveolar bone loss.

Macaca arctoides monkeys develop periodontal disease, and they harbor a periodontopathic indigenous flora largely similar to that of humans. This study showed that various Haemophilus isolates and H2O2-splitting asaccharolytic Bacteroides melaninogenicus strains constituted major segments of the monkey periodontal microflora. These organisms have not been previously identified among human isolates. Furthermore, the present data revealed that asaccharolytic B. melaninogenicus strains increased in proportion from a few percent to about 66% of the total isolates concomitant with the development of a significant loss of alveolar bone mass. Hence, this study strongly implicates B. melaninogenicus subsp. asaccharolyticus and closely related strains as important pathogens in actively destructive periodontal disease.

Alveolar Process↗

Quantitative analyses of osteoclast changes in resorbing bone organ cultures.

The stimulation of bone resorption, assessed by the release of 45Ca from prelabeled bones, was associated with an increase in number of osteoclasts per bone section in parathyroid hormone (PTH)-treated bones, but not in lipopolysaccharide (LPS)-treated bones. By contrast the number of nuclei per osteoclast increased following LPS treatment, but was not affected by PTH. LPS-treated bones had more multinucleated cells, some having as many as 27 nuclei per osteoclast. More osteoclasts were adjacent to the bone collar in bones treated with LPS or PTH than in control bones. In LPS-treated bones this area also contained the largest osteoclasts, as determined by the greatest number of nuclei per osteoclast. The results suggest that LPS and PTH stimulate osteoclastic resorption by different mechanisms.

Animals↗

The alteration of osteoclast morphology by diphosphonates in bone organ culture.

Two diphosphonates alter the morphology of the osteoclast, as they inhibit the calcium45 release from bones stimulated to resorb by lipopolysaccharide. Disodium dichloromethylene diphosphonate was more potent than disodium ethane-1-hydroxy-1, 1-diphosphonate in both inhibiting 45calium release and altering osteoclast morphology. Alteration in the morphology of osteoclasts is associated with little or no change in the morphology of the surrounding non-osteoclast cells. These results indicate a specific morphological effect of diphosphonates on osteoclasts.

Animals↗

Prostaglandins: bone resorption stimulating factors released from monkey gingiva.

Gingival fragments from monkeys have been found to release a factor in vitro into incubation medium which stimulates bone resorption in organ culture. Indomethacin effectively blocks the occurrence of this stimulatory factor in the gingival incubation medium. All of this bone resorptive activity can be accounted for by prostaglandin-like material. The prostaglandins contributing to the bone resorptive activity have been found to be prostaglandins E1 and E2.

Alveolar Process↗