1.5 Integration Of Metabolism Flashcards
What does muscle metabolise
Carbohydrate and fatty acid oxidation
What does the brain metabolise
Glucose (ketone bodies if needed)
Can’t utilise fatty acid
What does the heart metabolise
Fatty acids and carbs
Too little glucose
Hypoglycaemia
Causes faintness and coma
Too much glucose
Hyperglycaemia
Can cause irreversible damage
ATP requirement in skeletal muscle
Light contraction is met by oxphos
Vigorous contraction uses glycogen breakdown and lactate formation
Metabolic features of the heart
Completely aerobic metabolism
Rich in mitochondria
Utilises TCA cycle substrates (free fa and ketone bodies)
What levels should glucose be kept at
4-5.5mM
Glucose storage organ
Liver (glycogen)
During fasting Acetyl coA
Doesn’t enter TCA cycle but makes ketone bodies
Gluconeogenesis
Formation of glucose from pyruvate
Inputs to gluconeogenesis
Lactate from skeletal muscle converted to pyruvate by lactate dehydrogenase
Amino acids from diet or skeletal muscle
Glycerol converted to DHAP (triglyceride hydrolysis)
How is gluconeogenesis possible as the reversal of glycolysis
Energetically unfavourable so 6 bypass reactions (breaking of phosphoanhydride bonds to make it energetically favourable
Protein as fuel courses
Glucogenic amino acids generate glucose via gluconeogenesis
Ketogenic amino acids generate fatty acids and ketone bodies
Fats as fuel sources
Triglycerides broken down to fatty acids and glycerol
Fatty acids to ketone bodies
Enter gluconeogenesis