Glucose oxidation by developing rat intestine changed dramat- ically during the period of suckling and weaning. After weaning, glucose oxidation to C02 by intestinal slices increased over 3- fold. This was associated with an increase in lactate production from glucose and an increase in the rate of pyruvate decarbox- ylation. Active pyruvate dehydrogenase in intestine of developing rats also increases in activity at the time of weaning, suggesting that the suppression of glucose oxidation during the suckling period is controlled by pyruvate dehydrogenase. Glucose oxidation to CO2 and pyruvate decarboxylation to CO2 by intestinal slices of postweaned animals was inhibited by exogenous 3-hydroxvbutyr- ate. But exogenous 3-hydroxybutyrate did not inhibit glucose and pyruvate oxidation in intestine of suckling animals which have higher levels of endogenous 3-hydroxybutyrate than intestine of postweaned rats. Palmitate, in contrast, inhibited glucose and pyruvate oxidation by both pre- and post weaned intestine. © 1984 International Pediatric Research Foundation, Inc.
CITATION STYLE
Kimura, R. E., Thulin, G., & Warshaw, J. B. (1984). The effect of ketone bodies and fatty acid on intestinal glucose metabolism during development. Pediatric Research, 18(7), 575–579. https://doi.org/10.1203/00006450-198407000-00001
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