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• The liver maintains the proper levels of circulating fuels for use by
the brain, muscles, and other tissues.
• It is uniquely situated to carry out this task because all the nutrients
absorbed by the intestines except fatty acids are released into the
portal vein, which drains directly into the liver.
• Glucokinase Converts Blood Glucose to Glucose-6-Phosphate (One
of the liver’s major functions is to act as a blood glucose “buffer”).
• Glucose-6-Phosphate has several alternative fates in the liver,
depending on the glucose demand.
• The Liver Can Synthesize or Degrade Triacylglycerols.
• The liver degrades amino acids to a variety of metabolic
intermediates that can be completely oxidized to CO2 and H2O or
converted to glucose or ketone bodies
Metabolic fate of glucose-6-phosphate (G6P) in liver.
G6P can be converted (1) to glucose for export or (2) to glycogen for storage. Acetyl-CoA
derived from G6P degradation (3) is the starting material for lipid biosynthesis. It is also
consumed in generating ATP by respiration. Degradation of G6P via the pentose
phosphate pathway (4) yields NADPH.
Metabolism of amino acids in the liver
Metabolism of fatty acids in the liver
Blood Transports Metabolites in Interorgan
Metabolic Pathways
Pyruvate produced by muscle glycolysis is the amino-group acceptor for muscle aminotransferases. The
resulting alanine is transported by the bloodstream to the liver, where it is converted back to pyruvate (its
amino group is disposed of via urea synthesis). The pyruvate is a substrate for gluconeogenesis, and the
bloodstream carries the resulting glucose back to the muscles.
Hormonal Control of Fuel Metabolism