Examples of pyruvate

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Oxygen, glucose and pyruvate uptakes as well as lactate release were evaluated.
For this reason, pyruvate, hypotaurine, penicillamine and epinephrine were also were excluded from the media.
In the absence of the inhibitor, a direct relationship was seen between fluid accumulation and both glucose (but not pyruvate) consumption and lactate production.
Species-specific requirements of exogenous glucose and pyruvate and metabolic alteration among species were not directly elucidated in this study.
When available, glucose is taken up by the embryos at a high rate in comparison with pyruvate.
Developmentally related changes in the uptake and metabolism of glucose, glutamine and pyruvate by cattle embryos produced in vitro.
The rate of uptake of glucose and pyruvate can be related to their respective concentrations in the culture medium.
The kinetics of polar body formation were also fastest in pyruvate-containing medium.
The sensitivity of one-cell mouse embryos to pyruvate and lactate.
In the absence of glutamine, the addition of pyruvate to glucose-containing medium restored viability as well as supporting a high meiotic completion rate.
The total activity of this enzymatic reaction in cell-free worm systems could, however, not account for the rate of pyruvate decarboxylation observed with intact parasites.
Evidence in support of this suggestion was the finding that the rates of pyruvate decarboxylation in cell-free fractions showed considerable variation in different experimental studies.
The sensitivity of one cell regionalization in early mouse embryos as demonstrated mouse embryos to pyruvate and lactate.
The role of glucose and pyruvate transport in regulating nutrient utilisation by preimplantation mouse embryos.
The role of glucose and pyruvate transport in regulating nutrient utilization by preimplantation embryos.
As pyruvate is produced by glycolysis and consumed by gluconeogenesis, parasite-induced starvation of the host should result in a depletion of hepatocellular pyruvate.
In the absence of substrate, less than 9% of the oocytes survived, but viability was restored by either pyruvate or glucose.
In the absence of the energy substrates pyruvate, glucose and lactate, the number of blastocysts developing from morulae was reduced.

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