Ventricles from 11-day-old chick embryonic heart were disaggregated by elastase and the component cells cultured on glass in maintenance medium containing 10 pc of P3'. After 48 hours incubation at 37ยฐC the medium was removed, the cells rinsed and exposed to a phosphate-free test solution for two ho
Adenine nucleotide degradation in cultured chick heart muscle cells
โ Scribed by Bernhard Wagenknecht; Melvyn Lieberman
- Publisher
- Springer
- Year
- 1991
- Tongue
- English
- Weight
- 521 KB
- Volume
- 107
- Category
- Article
- ISSN
- 0300-8177
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โฆ Synopsis
Cultured chick heart muscle cells degrade ATP during metabolic inhibition via ADP to AMP. Whether AMP is primarily deaminated to IMP or dephosphorylated to adenosine depends on the 'metabolic block' (glycolysis vs. oxidative phosphorylation). Inhibition of glycolysis (deoxyglucose) results in an inosine/adenosine ratio greater than 1 in the supernatant, whereas the nucleoside ratio is less than or equal to 1 during inhibition of oxidative phosphorylation (hypoxia, rotenone). EHNA, a blocker of adenosine deaminase, has little effect on inosine release during metabolic inhibition, consistent with the reported low activity of adenosine deaminase in cardiac muscle cells. The amount of adenosine and inosine released can be largely attenuated by two nucleoside carrier inhibitors, nitrobenzyl-thioinosine and dipyridamole, which suggests that nucleosides are produced intracellularly and subsequently released. These results indicate that the amount of inosine or adenosine released from the cardiomyocyte during impaired energy metabolism (e.g. ischemia) can be controlled by the metabolic state of the cell.
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