About: Hycanthone is a research topic. Over the lifetime, 265 publications have been published within this topic receiving 4340 citations. The topic is also known as: Hycanthone & Lucanthone metabolite.
TL;DR: Worms that had been subjected to amoscanate or hycanthone in the third week after infection showed evidence of this as adults in having a reduced fecundity, and factors such as worm or host physiology, or host immune status may have had roles in the outcome of chemotherapy at different stages of maturation of S. mansoni.
TL;DR: The effect of host immunosuppression on the efficacy of schistosomicidal chemotherapy has been tested in T-cell-deprived CBA mice infected with Schistosoma mansoni, and the possibility that hycanthone, oxamniquine, praziquantel, and previously studied antimony act synergistically with immune effector mechanisms in killing adultschistosomes is discussed.
TL;DR: Following the administration of relatively high doses of the antischistosomal drug hycanthone to mice and hamsters infected with Schistosoma mansoni, a number of worms survived and this drug resistance has remained stable for three subsequent generations of worms.
Abstract: Following the administration of relatively high doses of the antischistosomal drug hycanthone to mice and hamsters infected with Schistosoma mansoni, a number of the worms survived. After a period of 6 to 12 months these parasites resumed production of viable eggs that gave rise to schistosomes that proved resistant to hycanthone and to two other related antischistosomal compounds. This drug resistance has remained stable for three subsequent generations of worms.
TL;DR: Comparative studies of WW and LE strains revealed marked differences in their sensitivity to the schistosomicides employed, although changes in oxamniquine and niridazole the changes were smaller although still quite sufficient to indicate greater resistance of WW strain to these schistoomicides.
Abstract: There has been isolated a Schistosoma mansoni strain from two patients submitted to two courses of treatment with hycanthone (2,5mg/kg, i.m.), in January and April, 1970, and to one course with niridazole (25mg/kg/day x 5, per os), in April, 1971. Before treatment, the number of eggs in the faeces of those patients was, per gram, 2,675 and 1,025, respectively; after completion of treatment, such number had come down to around 100 eggs/gram. Miracidia hatched from the patients faeces could infect Biomphalaria glabrata snails, which elimmated cercariae (WW strain) that were used for experimental infection of albino mice. The infected animais were, afterwards, treated with hycanthone, niridazole and oxamniquine under various schedules. Comparative studies of WW and LE strains (the latter being routinely kept in our laboratories) revealed marked differences in their sensitivity to the schistosomicides employed. Actually, after treatment with hycanthone, at the dosage of 80 mg/kg, i.m., a 100% oogram changes were observed in the intestinal wall of mice inoculated with LE strain, whereas no alterations could be detected in the mice infected with WW strain. As regards oxamniquine and niridazole the changes were smaller although still quite sufficient to indicate greater resistance of WW strain to these schistosomicides. It is worth while remembering that, in the pertaining literature, it is the first time that resistance in S. mansoni strains from treated patients has been demonstrated.