Related Experiment Videos
Plasma pool source for fibrinogen synthesis in postabsorptive conscious dogs
1Endocrine Research Unit, Mayo Clinic and Foundation, Rochester, Minnesota 55905.
The American Journal of Physiology
|April 1, 1991
Summary
Fibrinogen synthesis in dogs primarily uses leucine from the portal vein, not the hepatic artery. Alpha-ketoisocaproate (KIC) from the portal vein has minimal direct impact on fibrinogen production.
Area of Science:
- * Physiology
- * Biochemistry
- * Nutritional Science
Background:
- * Hepatic protein synthesis is crucial for physiological functions.
- * Understanding amino acid sources (portal vein vs. hepatic artery) is key to hepatic metabolism.
- * Leucine and alpha-ketoisocaproate (KIC) are important amino acid metabolites.
Purpose of the Study:
- * To determine the relative contributions of portal vein- and hepatic artery-derived leucine and KIC to hepatic protein synthesis.
- * To investigate the role of precursor pool origin in fibrinogen synthesis.
- * To explore potential zonation in hepatic amino acid metabolism.
Main Methods:
- * Simultaneous infusion of dual-labeled leucine or KIC tracers in postabsorptive dogs.
- * Tracers administered via leg vein (systemic) and mesenteric (portal) catheters.
- * Measurement of tracer radioactivity in plasma and fibrinogen-bound leucine.
Main Results:
- * Fibrinogen synthesis predominantly utilized leucine delivered via the portal vein.
- * Hepatic artery contribution to leucine for fibrinogen synthesis was negligible.
- * Intraportal KIC showed limited direct contribution to fibrinogen synthesis.
Conclusions:
- * Hepatic fibrinogen synthesis relies almost exclusively on portal vein-supplied leucine.
- * Hepatic artery does not significantly contribute leucine for fibrinogen production.
- * Findings support the concept of zonation in hepatic amino acid metabolism and protein synthesis.