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Biochemistry · Nucleotide metabolism: xanthine oxidase in reperfusion injury
Sample itemIn ischaemic tissue ATP is degraded and hypoxanthine accumulates. When blood flow returns, why is free radical injury produced?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
B. Xanthine oxidase oxidises hypoxanthine using oxygen and releases superoxide
During ischaemia xanthine dehydrogenase is converted to the oxidase form while ATP breaks down to hypoxanthine. On reperfusion, oxygen allows xanthine oxidase to convert hypoxanthine to xanthine and urate, generating superoxide and hydrogen peroxide.
Option by option
A. Uricase converts the accumulated urate to allantoin and hydrogen peroxide
Humans lack functional uricase, so this step does not occur.
B. Xanthine oxidase oxidises hypoxanthine using oxygen and releases superoxide (correct)
Correct. Reintroduced oxygen drives xanthine oxidase and the release of reactive oxygen species.
C. Adenosine deaminase converts hypoxanthine to uric acid without oxygen
Adenosine deaminase acts on adenosine, not hypoxanthine, and the oxidation to urate needs oxygen.
D. Hypoxanthine is salvaged to IMP and uses up all PRPP
Salvage to IMP needs PRPP but does not generate radicals and would help restore ATP.
Source note: Original NextPrep sample item — pending expert review. This item is original practice material awaiting independent expert review, so confirm important facts in a standard textbook.
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