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• W1992018786 abstract "We evaluated the antiemetic activity of resiniferatoxin, an ultrapotent capsaicin analogue, on cisplatin- and apomorphine-induced emesis in dogs, and on cisplatin-induced acute and delayed emesis in ferrets. In the dog, resiniferatoxin (10 μg/kg, s.c.) 30 min before the injection of cisplatin markedly prevented acute emesis induced by cisplatin. When animals were given resiniferatoxin (10 μg/kg, s.c.) 24 h prior to cisplatin, the emesis was still inhibited, but not significantly. Resiniferatoxin (10 μg/kg, s.c.) 30 min before the administration of apomorphine also significantly reduced the emetic responses induced by apomorphine in dogs. In the ferret, resiniferatoxin (10 μg/kg, s.c.) 30 min prior to cisplatin completely inhibited acute emesis caused by cisplatin (10 mg/kg, i.p.). When ferrets were given resiniferatoxin (10 μg/kg, s.c.) 16 h prior to cisplatin, the emesis was still significantly inhibited. Cisplatin (5 mg/kg, i.p.) induced both acute (0–24 h) and delayed (24–72 h) phase emesis, and a single injection of resiniferatoxin (10 μg/kg, s.c.) at 36 h after cisplatin significantly reduced subsequent emetic responses during the 36–72 h period. These results suggest that resiniferatoxin-related vanilloids may be useful drugs against both acute and delayed emesis induced by cancer chemotherapy." @default.
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• W1992018786 date "2002-05-01" @default.
• W1992018786 modified "2023-10-17" @default.
• W1992018786 title "Resiniferatoxin antagonizes cisplatin-induced emesis in dogs and ferrets" @default.
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• W1992018786 doi "https://doi.org/10.1016/s0014-2999(02)01541-8" @default.
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