A. Carbohydrate
B. Protein
C. Fat
D. All of the above
Related Mcqs:
- The total blood concentration of ketone bodies in well fed individual is__________?
A. 1 mg%
B. 5 mg%
C. 12 mg%
D. 20 mg% - The ketone bodies, which are excreted in diabetic ketoacidosis ?
A. Acetoacetic acid and pyruvic acid
B. Acetoacetic acid and oxalocacetic acid
C. Acetoacetic acid and alpha ketoglutaric acid
D. Acetoacetic acid and beta hydroxyl butyric acid - Ketone bodies are normally synthesized from______________?
A. Acetyl-CoA
B. Glucose
C. Glycerol
D. Acetone - Alkaptonuria, an inherited metabolic disorder of L0tyrosine metabolism is due to lack of_____________?
A. Parahydroxy phenyl pyruvate Hydroxylase
B. Tyrosine transaminase
C. Homogentisate oxidase
D. Tyrosine oxidase - Ketone body formation takes place in_______________?
A. Liver
B. Kidney
C. Spleen
D. Blood - Which of the following is not a ketone body______________?
A. Acetone
B. Acetic acid
C. Acetocetate
D. Beta hydroxybutyric acid - Which of the following organs cannot use ketone bodies_______________?
A. Brain
B. Liver
C. Kidney
D. Spleen - Reilly bodies are inclusion bodies seen in hurler’s disease within___________?
A. Lymphocytes
B. Fibroblast
C. RBC
D. WBC - HMG-CoA is formed during metabolism of all except______________?
A. Cholesterol
B. Leucine
C. Ketone bodies
D. Bile acids - Ligant for peroxisome proliferation activating receptor (PPAR) receptors, a group of nuclear hormone receptors that are involved in the regulation of genes related to glucose and lipid metabolism is_____________?
A. Repaglinide
B. Voglibose
C. Exanatide
D. Rosiglitgazone
