Hydrogen peroxide metabolism in alveolar macrophages after exposure to hypoxia and heat
Language English Country Czech Republic Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
16343036
DOI
10.33549/physiolres.930863
PII: 863
Knihovny.cz E-resources
- MeSH
- Macrophages, Alveolar cytology enzymology metabolism MeSH
- Nitrites metabolism MeSH
- Glucosephosphate Dehydrogenase metabolism MeSH
- Glutathione metabolism MeSH
- Glutathione Peroxidase metabolism MeSH
- Cell Hypoxia physiology MeSH
- Catalase metabolism MeSH
- Rats MeSH
- Cells, Cultured MeSH
- Thiobarbituric Acid Reactive Substances metabolism MeSH
- Hydrogen Peroxide metabolism MeSH
- Rats, Wistar MeSH
- Superoxide Dismutase metabolism MeSH
- Hot Temperature * MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Nitrites MeSH
- Glucosephosphate Dehydrogenase MeSH
- Glutathione MeSH
- Glutathione Peroxidase MeSH
- Catalase MeSH
- Thiobarbituric Acid Reactive Substances MeSH
- Hydrogen Peroxide MeSH
- Superoxide Dismutase MeSH
High temperature can change the effects of intra- and intercellular regulators and therefore modify the cellular response to hypoxia. We investigated H(2)O(2) production by alveolar macrophages, isolated from adult male rats, which were incubated under conditions of oxygen deficiency and high temperature (experiment in vitro). The incubation of these cells for 2 hours at 10 % or 5 % oxygen led only to slight fluctuations in the H(2)O(2) level, while the rise of temperature from 37 degrees C up to 42 degrees C significantly increased its generation. Level of thiobarbituric acid-reactive substances (TBARS) underwent similar changes. Under these conditions the accumulation of H(2)O(2) was found to be caused mainly by its decreased cleavage rather than its enhanced production. This is indicated by decreased catalase and glutathione peroxidase activity together with a parallel absence of significant changes in superoxide dismutase (SOD) activity. Slight fluctuation of reduced glutathione level and the pronounced increase of glucose-6-phosphate dehydrogenase (G6PD) activity were detected. Strong (5 %) but not moderate (10 %) lack of oxygen led to a sharp increase in formation of cellular nitrite ions by alveolar macrophages. In general, our data showed that high temperature did not lead to any qualitative shifts of defined hypoxia-derived changes in oxidant/antioxidant balance in alveolar macrophages, but promoted sensitivity of cells to oxygen shortage.
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