Objective. To study the in vitro effects of human haptoglobin (Hp) on bone resorption and prostanoid formation. Methods. Parietal bones were dissected out from neonatal mice that had been injected with '%a, and were cultured in chemically defined medium with or without test substances. Bone resorpt
Oxygen consumption of calvarial bone cells in vitro
β Scribed by K. Schirrmacher; S. Lauterbach; D. Bingmann
- Book ID
- 102914830
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- English
- Weight
- 523 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0736-0266
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Tissues with tortuous and narrow diffusion pathways and cells that are remote from blood vessels nonetheless can show high metabolic activity of which the underlying bases (transport mechanisms) are not fully understood. In one such bone tissue, the O~2~ consumption was measured by analyzing the decrease in the partial pressure of oxygen (PO~2~) in a closed chamber containing calvarial fragments from adult guinea pigs (250β400 g) or from neonatal rats and guinea pigs. The O~2~ consumption of fragments from adult guinea pigs amounted to 0.05. 0.066, and 0.095 ml/100 g * minute at 24. 27, and 36.5Β°C, respectively. When the temperature exceeded 43Β°C, O~2~ consumption irreversibly stopped. Both antimycin A and rotenone, which block the respiratory chain, reduced O~2~ consumption to approximately 20% of control values. O~2~ consumption was significantly higher in neonatal animals (0.369 ml/100 g * minute at 27Β°C) and could be blocked completely by antimycin A. On the basis of the high consumption of O~2~ by bone cells. we hypothesize that specialized transport systems, i.e., gap junctions, are required to provide a sufficient supply of nutrients to cells in osseous tissue.
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