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dc.contributor.authorMugera, GM
dc.contributor.authorWard, JM
dc.date.accessioned2015-07-28T16:07:05Z
dc.date.available2015-07-28T16:07:05Z
dc.date.issued1977
dc.identifier.citationCancer Treatment Reports [1977, 61(7):1333-1338]en_US
dc.identifier.urihttp://europepmc.org/abstract/med/563288
dc.identifier.urihttp://hdl.handle.net/11295/89080
dc.description.abstractThe toxicity of maytansine given by sc administration was studied in 5-week-old mald F344 rats. The LD50 (14-day) was 0.48 mg/kg. A dose response to drug administration was indicated by body weight changes and diarrhea. A single, acutely toxic dose of maytansine was shown to possess marked activity against dividing cells which was regarded as an important factor in the pathogenesis of acute lesions in tissues with a normal high rate of cell division. Histologically, mitotic figues were observed in many tissues from 6 to 24 hours after drug administration. Subsequently, necrotizing lesions led to atrophic changes in gastrointestinal tract mucosa, thymus, spleen, bone marrow, and testis. Maytansine also induced hemorrhagic lesions in parenchymatous organs and brain and perivascular monomuclear infiltration in the meninges, and chromatolysis and vacuolation of dorsal root ganglion cells, accompanied by clinical signs of ataxia. Ulcerative skin lesions were observed at the sc site of drug administration.en_US
dc.language.isoenen_US
dc.titleAcute toxicity of maytansine in F344 rats.en_US
dc.typeArticleen_US
dc.type.materialenen_US


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