Disorders of fatty acid oxidation include;
A. Carnitine deficiency
B. Carnitine deficiency
C. Ketoacidosis
D. All of the above
Answer: D
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A. Carnitine deficiency
B. Carnitine deficiency
C. Ketoacidosis
D. All of the above
Answer: D
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A. Thiolase
B. β-hydroxyacyl CoA dehydrogenase
C. Enoyl CoA hydratase
D. Acyl CoA dehydrogenase
Answer: A
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A. Oxidation of fatty acyl CoA
B. Hydration of the unsaturated fatty acyl CoA
C. Oxidation of the β-hydroxy derivative
D. None of the above
Answer: D
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A. Carnitine acyl transferase 1 facilitates synthesis of Acyl carnitine
B. Carninitine acyl translocase transports acyl carnitine across the inner mitochondrial membrane into the matrix
C. Mitochondrial Carnitine acyl transferase II re-synthesizes fatty acyl CoA
D. Free carnitine remains in the mitochondrial matrix
Answer: D
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A. Free fatty acids travels through the blood stream bound to serum albumin
B. Fatty acid activation occurs in the cytosol as fatty acyl CoAs
C. Fatty acid oxidation occurs in the mitochondrial matrix
D. None of the above
Answer: D
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A. Activation of intracellular second messenger cascade
B. Phosphorylation of hormone sensitive lipase
C. Lipolysis of triglycerides into glycerol and free fatty acids
D. None of the above
Answer: D
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A. Hepatic conversion of acetyl coA from FA oxidation
B. Amino acid breakdown to ketone bodies
C. Hepatic and skeletal muscle glycogenesis
D. Hepatic gluconeogenesis
Answer: C
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