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Factors affecting gluconeogenesis in the neonatal subhuman primate (Macaca mulatta)
Biology of the Neonate
|January 1, 1980
Summary
Newborn non-human primates show rising blood glucose with age. Despite adequate gluconeogenic substrates, low enzyme levels limit glucose production, but fatty acids correlate with glucose levels.
Area of Science:
- Biochemistry
- Neonatal Physiology
- Primate Metabolism
Background:
- Gluconeogenesis is vital for maintaining blood glucose homeostasis, especially in neonates.
- Subhuman primates (Macaca mulatta) serve as a valuable model for studying human neonatal metabolism.
- Understanding neonatal gluconeogenic capacity is crucial for identifying metabolic vulnerabilities.
Purpose of the Study:
- To investigate the capacity for gluconeogenesis in newborn Macaca mulatta.
- To correlate blood glucose levels with gluconeogenic substrate availability and enzyme activity.
- To examine the relationship between serum-free fatty acids and glucose metabolism in neonates.
Main Methods:
- Studied 33 newborn Macaca mulatta in a basal steady state.
- Measured basal blood glucose, alanine, lactate, and serum-free fatty acid levels.
- Assessed hepatic and renal cortical content of key gluconeogenic enzymes.
Main Results:
- Basal blood glucose levels increased with postnatal age.
- Adequate gluconeogenic substrates (alanine, lactate) were present even when glucose and gluconeogenesis rates were low.
- Key gluconeogenic enzyme levels were low in the first week compared to adults.
- Low enzyme induction did not fully explain low blood glucose; serum-free fatty acids correlated with glucose and gluconeogenesis.
Conclusions:
- Neonatal primate gluconeogenesis is limited by low key enzyme levels, not substrate availability.
- Serum-free fatty acids play a significant role in regulating neonatal glucose levels and gluconeogenesis.
- These findings highlight potential metabolic challenges in primate neonates requiring further investigation.