Chapter 1. Carbohydrates (17)
1.1. Glycolysis – Investment Phase
1.2. Glycolysis – Payoff Phase
1.3. Regulation of PFK-1 and FBPase-1 by F-2,6-BP and During the Fed and Fasting State
1.4. Gluconeogenesis
1.5. Pyruvate Dehydrogenase Complex
1.6. Fates of Pyruvate
1.7. Pyruvate Dehydrogenase Deficiency and Arsenic Poisoning
1.8. Hormonal Regulation of Glycogen by Insulin, Glucagon, and Epinephrine
1.9. TCA Cycle
1.10. Glycogen Synthesis (Glycogenesis) and Degradation (Glycogenolysis)
1.11. Malate-Aspartate and Glycerol-Phosphate Shuttles
1.12. Pentose Phosphate Pathway, G6PD Deficiency
1.13. Electron Transport Chain, Oxidative Phosphorylation
1.14. Metabolism and Disorders of Galactose
1.15. Metabolism and Disorders of Fructose and Sorbitol
1.16. Lactase Deficiency
1.17. Glycogen Storage Diseases
Chapter 2. Amino Acids And Proteins (10)
2.1. Amino Acids (Overview)
2.2. Amino Acid Derivatives
2.3. Catecholamine Synthesis and Degradation
2.4. Inborn Errors of Amino Acid Metabolism (Overview), Phenylketonuria (PKU)
2.6. Disorders of Tyrosine Catabolism, Alkaptonuria
2.7. Branched-Chain Amino Acid Catabolism, Maple Syrup Urine Disease
2.8. Urea Cycle, Hyperammonemia, Ornithine Transcarbamylase Deficiency
2.9. The Cahill and Cori Cycles
2.10. Organic Acidemias
2.11. Homocystinuria
Chapter 3. Lipids (7)
3.1. Triglyceride Catabolism, Beta Oxidation of Even-Chain Fatty Acids
3.2. Beta Oxidation of Odd-Chain Fatty Acids (VOMIT Pathway)
3.3. Ketone Bodies
3.4 Cholesterol Synthesis
3.5. Fatty Acid Synthesis
3.6 Lipid Digestion & Absorption
3.7 Lipid Transport (Key Enzymes, Major Apolipoproteins, and Lipoprotein Functions)
Chapter 4. Alcohol Metabolism (1)
4.1. Alcohol Metabolism
Chapter 5. Heme & Porphyrias (2)
5.1. Heme Synthesis
5.2. Porphyrias