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Rat heart mitochondria release adenosine.
Biochemical and Biophysical Research Communications
|June 29, 1983
Summary
Isolated rat heart mitochondria release adenosine, particularly when pyruvate + malate or rotenone are present at 30°C. This release is linked to the adenine nucleotide transporter and regulated by the mitochondrial ATP/ADP ratio.
Area of Science:
- Mitochondrial Physiology
- Biochemistry
- Cellular Respiration
Background:
- Mitochondria are crucial for cellular energy production.
- Adenosine release from mitochondria is not fully understood.
- Mitochondrial adenine nucleotide transporter (ANT) plays a key role in nucleotide exchange.
Purpose of the Study:
- To investigate the conditions and mechanisms of adenosine release from isolated rat heart mitochondria.
- To determine the relationship between mitochondrial respiration and adenosine release.
- To test the hypothesis that adenosine release is mediated by the ANT and regulated by the intramitochondrial ATP/ADP ratio.
Main Methods:
- Isolated rat heart mitochondria were used.
- Adenosine release was measured under various conditions including different temperatures (4°C vs. 30°C).
- The effects of respiratory substrates (pyruvate + malate), inhibitors (rotenone, oligomycin), atractyloside, 1799, calcium (Ca++), and oxygen concentration were assessed.
Main Results:
- Adenosine release was temperature-dependent, with higher release at 30°C compared to 4°C.
- Pyruvate + malate or rotenone significantly increased adenosine release at 30°C.
- State 3 respiration, atractyloside, and 1799 attenuated adenosine release, while oligomycin had a partial effect.
- Adenosine release was independent of Ca++ (200 microM) and low oxygen concentrations (down to 2 microM).
Conclusions:
- Mitochondrial adenosine release is facilitated by the adenine nucleotide transporter.
- The release is modulated by the intramitochondrial ATP to ADP ratio.
- Specific conditions, including the presence of certain substrates and inhibitors, influence adenosine efflux from mitochondria.