Review 1 Glycolysis Flashcards
Liver
Fatty acid, glucose, amino acid
Adipose Tissue
Fatty acid
Skeletal Muscle
At rest: Fatty acid
Exertion: Glucose
Heart Muscle
Fatty acid
Brain
Fed state: glucose
Starvation: ketone bodies/glucose
Kcal/cal (dry)
Carb
Protein
Fat
Carb=4
Protein=4
Fat=9
Glycogenolysis
Glycogen–>Glucose
Stim: Glucagon, Epinephrine, Starve State
Glycogenesis
Glucose–>Glycogen
Stim: Insulin, Fed State
Glycolysis
Glucose–>Lactate and Pyruvate
Stim: Insulin, Fed State
Gluconeogenesis
Non carb products–>Glucose
Stim: Glucagon, Epinephrine, Starve State
3 stages to glycolysis
Priming Stage(ATP investment) Splitting Stage Oxidoreduction-phosphorylation stage (ATP earnings)
3 irreversible enzymes of glycolysis
- Hexokinase/Glucokinase
Glucose–>Glucose 6 phosphate - PFK-1
Fructose 6-phosphate–>Fructose 1,6 bisphosphate - Pyruvate Kinase
Phosphoenolpyruvate–>
2 Pyruvate
Hexokinase vs. Glucokinase
Hexokinase: All cell types, inhibited by glucose-6-phosphate, constitutive enzyme, low Km
Glucokinase: Liver and pancreas, Translocation between nucleus and cytosol, Fructose 6-P promotes translocation to nucleus(inactive), Glucose promotes translocation to cytosol(active), Inducible enzyme: enzyme synthesis increased by insulin, High Km
Pyruvate Carboxylase Genetic Deficiency
increase in blood alanine, lactate and pyruvate levels
Diagnosis: Developmental Delay, Recurrent Seizures, Metabolic Acidosis
Pyruvate Dehydrogenase Deficiency (PDH) genetic deficiency
Increases circulatory pyruvate and lactate concentration
Diagnosis: reduced head circumference (microcephaly), poor muscle coordination, and mental retardation