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  • Articles  (14)
  • Articles: DFG German National Licenses  (14)
  • Latest Papers from Table of Contents or Articles in Press
  • Bone resorption  (14)
  • Springer  (14)
  • American Chemical Society (ACS)
  • 2020-2024
  • 2015-2019
  • 1980-1984  (14)
  • 1970-1974
  • 1965-1969
  • 1935-1939
  • 1984  (8)
  • 1983  (6)
  • 1968
  • 1935
  • Physics  (14)
  • Economics
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  • Articles  (14)
Source
  • Articles: DFG German National Licenses  (14)
  • Latest Papers from Table of Contents or Articles in Press
Publisher
  • Springer  (14)
  • American Chemical Society (ACS)
Years
  • 2020-2024
  • 2015-2019
  • 1980-1984  (14)
  • 1970-1974
  • 1965-1969
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  • 1
    ISSN: 1432-0827
    Keywords: Diphosphonate ; EHDP ; Bone resorption ; Bone formation ; Chicks
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary Chicks chronically prelabelled with45Ca,3H-tetracycline, and3H-proline were used to measure the weekly effect of EHDP (5 mg P/kg for 28 days) on bone turnover at the whole bone level in vivo. Direct measurements were made of cortical bone resorption (loss of3H-tetracycline and3H-collagen from whole femur, blood-bone ratio of45Ca), skeletal collagen formation and bone mineralization (collagen and calcium mass per whole femur, respectively). Chicks were sacrificed after 5, 14, 21 and 28 days of EHDP administration. By five days of treatment, EHDP caused a greater inhibition of bone mineralization (86%) than bone resorption (30–39%) without affecting skeletal collagen mass. The blood-bone ratio of45Ca decreased 34%, which was similar in degree to the inhibition of3H-tetracycline loss (30%) and3H-collagen loss (39%). Almost complete inhibition of bone resorption and bone mineralization occurred by 14 days of treatment without effects on skeletal collagen mass. No additional effect was seen at 21 and 28 days of EHDP treatment. In chicks, EHDP inhibits almost completely bone mineralization (bone formation) and cortical bone resorption without affecting skeletal collagen mass.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Calcified tissue international 36 (1984), S. 556-558 
    ISSN: 1432-0827
    Keywords: Osteoclast ; Bone resorption ; Mononuclear phagocytes ; Monocytes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary Monocytes, peritoneal macrophages, inflammatory polykaryons, and myeloid cell lines were incubated on slices of human cortical bone and assessed for their capacity to resorb bone by scanning electron microscopy. None of these cell types, mononuclear or multinucleate, induced any detectable change in the bone surface, even after prolonged incubation, and even in the presence of macrophage activators. These findings emphasise the inadequacies of mononuclear phagocytes as surrogate osteoclasts, and expose a discrepancy between45Ca release and bone resorption.
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  • 3
    ISSN: 1432-0827
    Keywords: PTH ; PTH inhibitor ; Cyclic AMP ; Bone resorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary The effects of bPTH-(1-84), bPTH-(1-34), [Nle-8, Nle-18, Tyr-34] bPTH-(1-34), bPTH-(1-34) amide (NTA 1-34, desamino bPTH-(1-34), bPTH-(2-34), bPTH-(3-34), and [Nle-8, Nle-18, Tyr-34] bPTH-(3-34) amide (NTA 3-34) were tested in cultured bone cells, isolated from the osteoblast layers of fetal chicken calvaria (cyclic AMP) and in fetal rat calvaria (cyclic AMP, Ca release, and lactate production). Only bPTH-(1-84), bPTH-(1-34), and NTA 1-34 increased cyclic AMP production in a doserelated manner, both in calvaria and in bone cells, whereas all fragments (except NTA 3-34) stimulated bone resorption, the order of decreasing potency being bPTH-(1-84), NTA 1-34, bPTH-(1-34), desamino bPTH-(1-34), bPTH-(2-34), bPTH-(3-34). As in human cells, the antagonist NTA 3-34 inhibited specifically and in a dose-dependent way the cyclic AMP response of maximal concentrations of both bPTH-(1-84) and bPTH-(1-34) in rat calvaria and in chicken bone cells, when measured after short (15 min) and longer (1 1/2–16 h) incubation periods. In addition, measured after 4 h of incubation, NTA 3-34 completely inhibited bPTH-(1-84)-stimulated Ca release using maximal and submaximal concentrations. However, after 6–24 h of incubation, NTA 3-34 had no effect on bPTH-(1-84)-stimulated Ca and lactate release, even at an antagonist/agonist ratio up to 12.5 M, perhaps due to its lower affinity for the PTH receptor. From these findings we propose that (a) in bone there are two types of receptors, one governing demineralization via regulation of the calcium influx and one governing adenylate cyclase activity, and (b) the receptors are different from each other with respect to their affinities toward the agonists and the antagonist.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Calcified tissue international 36 (1984), S. 189-193 
    ISSN: 1432-0827
    Keywords: Protamine ; Hypocalcemia ; Parathyroid hormone ; Bone resorption ; Bone turnover
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary Protamine is shown to be a powerful disrupter of calcium homeostasis, acutely inducing a severe hypocalcemia in both rabbits and rats. The magnitude of its effect correlates with bone turnover. Protamine does not significantly alter the renal excretion of calcium, and is effective whether or not there is calcium present in the gut. Protamine causes a significant fall in the specific activity of45Ca in the blood in animals whose bone has been prelabeled with45Ca. These data suggest that protamine induces hypocalcemia by blocking calcium efflux from bone. Further work seems indicated to define the biochemical mechanism of this action.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Calcified tissue international 36 (1984), S. 182-188 
    ISSN: 1432-0827
    Keywords: Osteoclast ; Alveolar bone ; Bone resorption ; Differential response
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary Using a histochemical method for demonstrating acid phosphatase activity, we have studied osteoclasts residing at two different bone sites in rat incisor alveolar bone, one at the endosteum and the other at the tooth socket, and compared the response of these osteoclasts to systemic changes. After 12 days of calcium (0%) or phosphorus (0.2%) deprivation, the number of osteoclasts/cross section at the endosteum increased 463% (P〈0.001) and 103% (P〈0.002), respectively. After 10 days of calcium or phosphorus replenishment, the number of osteoclasts at this bone site decreased to levels not significantly different from those in the control. In contrast, the number of osteoclasts at the incisor socket remained insignificantly changed throughout the experimental period. A similar osteoclast differential response was also observed in the alveolar bone surrounding the first molar tooth. After 12 days of calcium deprivation, the number of osteoclasts/mm bone surface increased 371% (P〈0.001) at the endosteum but remained insignificantly changed at the first molar socket. These results suggest that an osteoclast differential response exists in alveolar bone and that the response may be of significance inasmuch as the major function of alveolar bone is to support the teeth. The work described here supports the concept of local as well as systemic regulation of bone metabolism to simultaneously perform the dual functions of mineral homeostasis and mechanical support.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Calcified tissue international 36 (1984), S. 722-724 
    ISSN: 1432-0827
    Keywords: Bone resorption ; Osteoblasts ; Collagenase ; Collagenase inhibitor ; Concanavalin A
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary Cultures of osteoblast-like cells from a rat sarcoma and osteoblast-enriched populations of rat calvarial cells synthesize and secrete a true collagenase and collagenase inhibitor. The enzyme, which is produced in a latent form, appears to be similar to the enzyme produced by fibroblasts.
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  • 7
    ISSN: 1432-0827
    Keywords: Tumor ; Hypercalcemia ; Humoral ; Bone resorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary A transplantable nonmetastasizing Leydig cell tumor, which occurs spontaneously in the aged Fischer rat, was examined bothin vitro andin vivo. Animals carrying this tumor were found to have the syndrome recently called thehumoral hypercalcemia of malignancy, characterized by hypercalcemia, hypercalciuria, hypophosphatemia, renal phosphate wasting, increased urinary 3′5′-cyclic monophosphate (cyclic AMP) excretion, and suppressed circulating parathyroid hormone (PTH) concentrations. The changes in urinary cyclic adenosine monophosphate (cAMP) excretion occurred simultaneously with hypercalcemia in most animals. In one animal, the primary tumor was excised and this was followed by an immediate fall in serum calcium and urine cAMP excretion. Hypercalcemia was due to increased bone resorption. This was shown by bone histology, which demonstrated an increase in osteoclast number and activity on trabecular bone surfaces associated with bone loss in tumor-bearing animals. No tumor cells were seen adjacent to the osteoclasts. There was no evidence of metastatic disease as assessed by bone-seeking isotopes. Urinary hydroxyproline excretion was increased in tumor-bearing hypercalcemic animals, indicating an increase in bone turnover. The tumor cells were established in culture and found to produce a bone-resorbing factorin vitro using a bioassay for bone resorption based on the release of previously incorporated45Ca from fetal rat long bones in culture. This model of the humoral hypercalcemia of malignancy should make it possible to determine the nature of the boneresorbing factor produced by the cultured tumor cells which is responsible for the hypercalcemia, and the relationship of hypercalcemia and the production of the bone-resorbing factor to the other parameters of the syndrome, namely, renal phosphate wasting and increased urinary cAMP excretion.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Calcified tissue international 35 (1983), S. 392-393 
    ISSN: 1432-0827
    Keywords: Osteoporosis ; Infrared ; Bone mineral ; Bone resorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary An infrared and x-ray diffraction study of osteoporotic and normal, archaeological Eskimo bones. Osteoporotic bone apatite is greater in crystal size and/or perfection and lower in CO3 than normal bone apatite.
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  • 9
    ISSN: 1432-0827
    Keywords: Age ; Bone resorption ; Hyperparathyroidism ; Renal osteodystrophy ; Sex
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary The severity and incidence of subperiosteal and intracortical bone resorption were evaluated from fine-detail hand radiographs at × 8 magnification in relation to age and sex in 239 chronically dialyzed adult renal failure patients. The severity of subperiosteal resorption decreased significantly with advancing age in both sexes and the incidence decreased somewhat more in males than in females; no such trends were apparent for intracortical resorption. Although the mean values for the grades of subperiosteal and intracortical resorption were significantly higher in females than in males, when the effect of age and duration of follow-up were taken into consideration, this sex difference remained significant only for intracortical resorption. It is concluded that when studying certain aspects of renal osteodystrophy, differences due to age, sex, and duration of follow-up should be considered in the final interpretation of data.
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Calcified tissue international 35 (1983), S. 294-297 
    ISSN: 1432-0827
    Keywords: Prostaglandins ; Osteoblasts ; Bone resorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary The metabolism of arachidonic acid to its cyclo-oxygenase products was studied in monolayer cultures of osteoblast-rich rat calvarial cells and of clonal cell lines from a rat osteogenic sarcoma, enriched in the osteoblast phenotype. Prostanoids were measured by radioimmunoassay after extraction of media and fractionation by high pressure liquid chromatography. In both normal and malignant osteoblasts the major cyclo-oxygenase product was 6-oxo-prostaglandin F1α, the hydration product of prostacyclin, with lesser amounts of prostaglandin E2 and prostaglandin F2α. No significant thromboxane B2 was detected. Prostaglandins are thought to have a local role in the regulation of bone resorption. These results point to the possible importance of prostacyclin either in bone resorption or in some other local function, e.g., regulation of bone blood flow.
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