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Broering, P

45 Ca 2+ release is partially blocked by co-treatment with the ryanodine receptor inhibitor, ruthenium red ( 3 H]ryanodine binding within the SR membranes and markedly increase skeletal muscle ryanodine receptor (RyR1) open probability ( 3 H]ryanodine binding or the rapid 45 Ca 2+ release induced by LCAC treatment (Yamada et al., 2000)

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Secondly, PC provides a source of propionyl units which are easily transformed into succinate for mitochondrial utilization in the citric acid cycle as a source of anaplerotic energy