Q.P. Code: 526055
Q.P. Code: 526055
com
[MBBS 1123] NOVEMBER 2023 Sub. Code : 6055
M.B.B.S. DEGREE EXAMINATION
(For the candidates admitted from the Academic Year 2019-2020)
and urine sugar compound that yielded a positive reducing-sugar test but was negative
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when measured with glucose oxidase. Treatment of the urine and serum with acid to
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cleave glycosidic bonds did not increase the amount of reducing sugar measure Which
of the following compounds is most likely to be present in this infant’s urine and serum?
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5. Proton pump inhibitors are a mainstay in the treatment of peptic ulcer disease and inhibit
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the gastric hydrogen ATPase. The hydrogen ATPase in the gastric mucosal parietal cell
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utilizes this energy to exchange one hydrogen ion from the cytoplasm for one
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6. Allopurinol is used in the treatment of gout because of its ability to inhibit xanthine
oxidase. This inhibition makes it impossible for the enzyme to degrade xanthine and
hypoxanthine, which reduces the synthesis of urate, the culprit of gout. Allopurinol works
through which one of the following mechanisms?
A) Suicide inhibition
B) Non-competitive inhibition
C) Allosteric interaction with the enzyme that increases Vmax
D) Feedback inhibition
7. A 47-year-old obese man complains of having to get out of bed three times a night to
urinate (polyuria), being constantly thirsty (polydipsia), and eating more often
(polyphagia). The patient is diagnosed with insulin- resistant diabetes mellitus (type 2).
If the patient’s symptoms are due to a problem at the level of the glucose transporter,
which one of the tissues indicated below will be most affected?
A) RBCs B) Muscle
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8. A 24-year-old woman presents with diarrhea, dysphagia, jaundice, and white transverse
lines on the fingernails (Mee lines). The patient is diagnosed with arsenic poisoning,
which inhibits which one of the following enzymes?
A) Isocitrate dehydrogenase B) Pyruvate dehydrogenase
C) Malate dehydrogenase D) Succinate dehydrogenase
9. A 3-year-old boy presents to the pediatric clinic with the symptoms of hypotonia, lactic
acidosis, and seizures. After an extensive workup, he is diagnosed with PDHC
deficiency, an X-linked recessive disorde Which one of the following cofactors is not
required by this enzyme to convert pyruvate to acetyl CoA?
A) Thiamine B) Lipoic acid C) Pantothenate D) Ascorbic acid
13. The rationale for the treatment of patient having gallstones with chenodeoxycholic acid is
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19. A patient presents in your office with very high levels of serum cholesterol. He states that
he has tried to follow the diet and exercise regimen you gave him last yea You decide
that this patient would benefit from a drug such as atorvastatin. This class of drugs is
effective in treating hypercholesterolemia because it has what effect.
A) Stimulates phosphorylation of the β-hydroxy-β-methylglutaryl-CoA reductase
enzyme (HMG CoA reductase)
B) Binds cholesterol preventing it from being absorbed by the intestine
C) Directly prevents the deposition of cholesterol on artery walls
D) Inhibits the enzyme β-hydroxy-β-methylglutaryl-CoA reductase (HMG CoA
reductase)
20. Criggler Najjar syndrome type 1 is a genetic disorder associated with unconjugated
hyperbilirubinemia. What enzyme deficiency is responsible for the disease?
A) Heme oxygenase B) Biliverdin reductase
C) UDP-glucuronosyltranseferase D) G-6 -phosphate dehydrogenase.
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