First, I need to recall what drug inhibits ODC. Ornithine decarboxylase is involved in the synthesis of polyamines, which are necessary for cell growth. Inhibiting ODC would slow down cell proliferation. The only drug I remember that does this is Eflornithine. It's used topically for hirsutism because it reduces hair growth by inhibiting ODC in the hair follicles.
Now, the question is about parasitic infections. Eflornithine is also used in the treatment of African trypanosomiasis, specifically caused by Trypanosoma brucei. The parasite relies on ODC for polyamine synthesis, so inhibiting it is toxic to the parasite. This makes Eflornithine effective against this infection.
Looking at the options, the possible parasitic infections could be African sleeping sickness (Trypanosoma brucei), leishmaniasis, or others. Since Eflornithine is specifically used for Trypanosoma brucei, that's the answer here. The other options, like Leishmania or other parasites, might use different mechanisms, so they wouldn't be treated with Eflornithine.
The key here is connecting the enzyme inhibition to both the topical use for hirsutism and the parasitic infection. The drug's dual use is important for the answer. So the correct answer should be African trypanosomiasis caused by T. brucei.
**Core Concept**
Ornithine decarboxylase (ODC) inhibition is a key therapeutic mechanism in both dermatology and parasitology. Eflornithine, an irreversible ODC inhibitor, is used topically for hirsutism and intravenously for African trypanosomiasis caused by *Trypanosoma brucei gambiense*.
**Why the Correct Answer is Right**
Eflornithine inhibits ODC, which catalyzes the first step in polyamine synthesis. In hirsutism, this blocks hair follicle growth. In *Trypanosoma brucei*, polyamines are essential for DNA synthesis and cell proliferation. By depleting polyamines, Eflornithine induces parasite death. It is specifically effective against *T. b. gambiense*, not other parasites or protozoa.
**Why Each Wrong Option is Incorrect**
**Option A:** Leishmaniasis is treated with pentavalent antimonials, amphotericin B, or miltefosine—not ODC inhibitors.
**Option B:** Malaria is managed with artemisinin-based therapies, not ODC-targeting drugs.
**Option C:** Giardiasis uses metronidazole or tinidazole, which act via different mechanisms (DNA damage, not polyamine inhibition).
**Clinical Pearl / High-Yield Fact**
Eflornithine is a high-yield drug for NEET
Free Medical MCQs · NEET PG · USMLE · AIIMS
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