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  • 1
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Physiology 43 (1981), S. 225-238 
    ISSN: 0066-4278
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Medicine , Biology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Medicine 29 (1978), S. 23-29 
    ISSN: 0066-4219
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Medicine 40 (1989), S. 251-267 
    ISSN: 0066-4219
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Pharmacology 12 (1972), S. 337-352 
    ISSN: 0362-1642
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Medicine , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of periodontal research 21 (1986), S. 0 
    ISSN: 1600-0765
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: The effects of human gingival extracts on in vitro, bone resorption were examined and related to the amount of plaque, gingival inflammation and bone resorption present at the time of sampling. Twenty patients with varying degrees of periodontal disease were used in this study. The plaque index and bleeding index were recorded. the marginal gingiva removing surgically and immediately freeze dried. Alveolar bone resorption was then measured from the cemento enamel junction (CFI) to the alveolar bone crest directly during surgical exposure or on radiographs. The bone resorting activity of extracts from freeze dried gingiva was then tested in an in vitro bone resorption assay. No bone resorting activity was noted in 17 of the 18 extracts tested and thus no correlation could be found with the clinical indices. Mean values of the T/C ratios for 18 extracts tested indicate a biphasic suppression of control resorption by the extracts. The extracts suppressed resorption stimulated by known bone resorbing agents. H [eating of the extract prior to testing eliminated this suppressive effect. It is concluded that inhibitors of bone resorption are present in human gingival extracts. Their presence may explain our inability to demonstrate bone resorhing activity in human gingiva.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of periodontal research 16 (1981), S. 0 
    ISSN: 1600-0765
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Twenty-four beagle dogs were divided into three groups of eight dogs each. Periodontitis was induced in three of the denial quadrants of each dog using wire ligatures while one quadrant was not ligaled and was kept cleaned. One group of dogs received no additional treatment, one group received systemic metronidazole and the third group received systemic indomethacin. The in vitro bone resorbing activity of extracts from freeze dried gingiva from the groups was compared.Extracts of gingiva from ligaled teeth produced significant bone resorption. Metronidazole treatment suppressed this ligature-induced bone resorbing activity while indomethacin had no effect. Extracts from gingiva from around clean non-ligated teeth had somewhat less activity than extracts from gingiva of ligaled teeth, although some significant resorption remained in all treatment groups. Bacterial cultures from melronidazoletreated groups showed a change from a predominantly Gram negative obligatory anerobic flora (B. assacharolyticus), to one predominated by Gram negative, facultative anaerobes (Capnocytophaga and Campylobacter). It was concluded that metronidazole suppressed bone resorbing activity by inducing a change in the flora of the gingival crevice.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Calcified tissue international 34 (1982), S. 270-272 
    ISSN: 1432-0827
    Keywords: Parathyroid hormone ; Minipumps ; Bone resorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary To determine if osmotic minipumps can be used for the local delivery of parathyroid hormone (PTH), we examined the bone resorbing activity of PTH in minipumps, either removed and assayed in bone organ cultures or released over rat calvaria. Biological activity of PTH was maintained for up to 6 days when the hormone solution contained serum and the minipumps and tubing were siliconized and flushed with diluent prior to use. Addition of cysteine did not enhance activity.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Osteoporosis international 4 (1994), S. S53 
    ISSN: 1433-2965
    Keywords: Bone turnover ; Bone markers ; Bone density ; Risk assessment ; Osteoporosis prevention
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Osteoporosis prevention programs, based on risk assessment, are an important goal both for individual patients and for improved public health. I have reviewed some of the current approaches to such programs and the major questions which must be answered in order to validate these approaches. In particular, new knowledge concerning the usefulness of markers of bone turnover and of the effectiveness of antiresponsive strategies should greatly improve our ability to prevent osteoporotic fractures. Meanwhile, there is enough information to support the concept that risk assessment should be used to develop a cost-effective prevention program and to guide the approach to therapy.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1433-2965
    Keywords: Bone alkaline phosphatase ; Deoxypyridinoline crosslinks ; N- telopeptide of type I collagen ; Osteocalcin ; Parathyroid hormone ; Type I procollagen peptide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Calcium and vitamin D (1200 mg/day + 800 IU) has been shown to reduce hip fracture incidence in older women living in long-term care facilities who had borderline low vitamin D levels. We examined the effect of a short course of calcium and vitamin D on biochemical markers of bone turnover in older community-living women. Twelve community-living women (mean age 75 years) in good general health, without diseases or on medications known to affect bone, were entered into the study. All women were treated with calcium citrate (1500 mg/day of elemental calcium) and vitamin D3 (1000 IU/day) (Ca + D) for 6 weeks. Biochemical markers of bone turnover were measured in serum and urine collected at baseline (two samples), 5 and 6 weeks on Ca + D, and 5 and 6 weeks after termination of Ca + D. Markers of bone formation were osteocalcin, bone alkaline phosphatase and type I procollagen peptide. Markers of bone resorption were urinary hydroxyproline, free pyridinoline and deoxypyridinoline crosslinks, and N-telopeptides of type I collagen. Parathyroid hormone (PTH) and 25-hydroxyvitamin D were also measured at baseline, 6 weeks on treatment and 6 weeks after termination of treatment. All markers of bone resorption decreased on Ca + D and returned to baseline after termination of Ca + D (p〈0.05). Markers of bone formation did not change with Ca + D treatment. PTH decreased on Ca + D and returned to baseline after treatment, and 25-hydroxyvitamin D increased with treatment and remained elevated 6 weeks after the end of treatment. We conclude that Ca + D reduces bone resorption in older women, possibly by suppressing PTH levels.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Osteoporosis international 3 (1993), S. 136-140 
    ISSN: 1433-2965
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Prostaglandins (PGs), particularly PGE2, are produced by bone and have powerful effects on bone metabolism. PGs have an initial, transient, direct inhibitory effect on osteoclast function. However, the major long-term effect in bone organ culture is to stimulate bone resorption by increasing the replication and differentiation of new osteoclasts. PGs also stimulate osteoclast formation in cell culture systems. Stimulation of osteoclastic bone resorption may be important in mediating bone loss in response to mechanical forces and inflammation. PGs have a biphasic effect on bone formation. At relatively low concentrations or in the presence of glucocorticoids, the replication and differentiation of osteoblasts is stimulated and bone formation is increased. This increase is associated with an increase in production of insulin-like growth factor-I (IGF-I). However, at high concentrations or in the presence of IGF-I, PGE2 inhibits collagen synthesis. In osteoblastic cell lines this inhibition can be shown to occur at the level of transcription of the collagen gene. The stimulatory effect on bone formation has been demonstrated when PGs are administered exogenously, but it is not clear how endogenous PG production affects bone formation in physiological or pathologic circumstances. The production of PGs in bone is highly regulated. The major source appears to be cells of the osteoblast lineage. A major site of regulation is at the level of the enzyme PG endoperoxide synthase (cyclooxygenase or PGH synthase). PGE2 production and PGH synthase mRNA are increased by PTH and interleukin-1 and decreased by estrogen. Glucocorticoids probably act by a different mechanism, decreasing either arachidonic acid or PGH synthase activity. Many other factors including mechanical forces and growth factors influence PG production in bone. Thus endogenous PGs are probably important local regulators of bone turnover, and abnormalities in their production could play a role in the pathogenesis of osteoporosis.
    Type of Medium: Electronic Resource
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