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Glutamate interconversions and glucogenicity in the sheep
The American Journal of Physiology
|December 1, 1981
Summary
This study reveals how sheep utilize glutamate, a key amino acid, for energy and glucose production. Acidosis and fasting significantly alter glutamate metabolism, impacting liver and hindquarter functions.
Area of Science:
- Metabolic Physiology
- Animal Nutrition
- Biochemistry
Background:
- Glutamate is a crucial amino acid involved in various metabolic pathways.
- Understanding glutamate metabolism is vital for animal health and physiological regulation.
Purpose of the Study:
- To quantify net and unidirectional glutamate metabolism in different ovine tissues.
- To assess the contribution of glutamate to glutamine and glucose production under varying physiological states.
- To investigate the impact of acidosis and fasting on glutamate flux and interconversion.
Main Methods:
- Simultaneous measurement of net and unidirectional glutamate flux in portal-drained viscera, liver, kidneys, and hindquarters of sheep.
- Utilized radiolabeled [14C]glutamate to trace metabolic pathways.
- Compared glutamate metabolism in fed, acidotic, and fasted states.
Main Results:
- Blood glutamate concentrations decreased with acidosis and fasting.
- Liver was a major source of plasma glutamate in fed sheep, while hindquarters utilized it; both fluxes were reduced by nutritional and acid-base challenges.
- Acidosis and fasting predominantly affected hepatic glutamate production and hindquarter utilization.
- Glutamate conversion to glutamine was low (12-25%), with most occurring extrarenally.
- Glutamate contributed significantly to glucose production (20-26%), with kidneys playing a key gluconeogenic role, especially during acidosis and fasting (40-45%).
Conclusions:
- Glutamate metabolism is significantly altered by acidosis and fasting in sheep.
- The liver and hindquarters show altered glutamate flux in response to physiological stress.
- Kidneys play a substantial gluconeogenic role, particularly under conditions of acidosis and fasting.