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dc.contributor.authorHoyes, Katherine P
dc.contributor.authorSharma, Harbans L
dc.contributor.authorJackson, H
dc.contributor.authorHendry, Jolyon H
dc.contributor.authorMorris, Ian D
dc.date.accessioned2010-04-09T09:14:05Z
dc.date.available2010-04-09T09:14:05Z
dc.date.issued1994-08
dc.identifier.citationSpermatogenic and mutagenic damage after paternal exposure to systemic indium-114m. 1994, 139 (2):185-93 Radiat. Res.en
dc.identifier.issn0033-7587
dc.identifier.pmid8052694
dc.identifier.urihttp://hdl.handle.net/10541/96084
dc.description.abstractThe cytotoxic and mutagenic consequences of systemic administration of 114mIn have been examined. Adult male rats were dosed intraperitoneally with 14.8 or 3.7 MBq/kg 114mIn. Approximately 0.25% of the injected radioactivity was localized within the testis by 24 h and was retained with an effective half-life of 49.5 days. Breeding studies were started 3 days after injection, males being housed with two females for seven consecutive mating trials of 19 days, separated by 2 days. Indium-114m caused a reduction in litter size and an increase in the incidence of pre- and postimplantation losses and dominant lethal mutations. These effects became evident from 24 days but were most marked between 87-126 days after treatment and persisted up to 147 days. When animals were mated 200 days after treatment, no significant changes were observed. In a parallel study, administration of 14.8 MBq/kg 114mIn resulted in decreased testis and epididymal weight and sperm reserves. Maximal reduction occurred between 87-108 days after injection followed by recovery toward control values, but neither organ had reached normal levels at 200 days. A single dose of 3.7 MBq/kg, however, had no effect on reproductive organ weight or sperm content. Male F1 progeny from the 14.8 MBq/kg group of the second mating period (commencing at 24 days) displayed decreased testis weights and sperm content and provoked a higher incidence of dominant lethal mutations. This effect was not observed in male progeny from any other time or the alternative dose level.
dc.language.isoenen
dc.subject.meshAnimals
dc.subject.meshBody Weight
dc.subject.meshIndium Radioisotopes
dc.subject.meshInfertility, Male
dc.subject.meshLitter Size
dc.subject.meshMale
dc.subject.meshMutation
dc.subject.meshOrgan Size
dc.subject.meshRadiation Dosage
dc.subject.meshRats
dc.subject.meshRats, Sprague-Dawley
dc.subject.meshSpermatogenesis
dc.subject.meshTestis
dc.titleSpermatogenic and mutagenic damage after paternal exposure to systemic indium-114m.en
dc.typeArticleen
dc.contributor.departmentDepartment of Experimental Radiation Oncology, Paterson Institute for Cancer Research, Manchester, United Kingdom.en
dc.identifier.journalRadiation Researchen
html.description.abstractThe cytotoxic and mutagenic consequences of systemic administration of 114mIn have been examined. Adult male rats were dosed intraperitoneally with 14.8 or 3.7 MBq/kg 114mIn. Approximately 0.25% of the injected radioactivity was localized within the testis by 24 h and was retained with an effective half-life of 49.5 days. Breeding studies were started 3 days after injection, males being housed with two females for seven consecutive mating trials of 19 days, separated by 2 days. Indium-114m caused a reduction in litter size and an increase in the incidence of pre- and postimplantation losses and dominant lethal mutations. These effects became evident from 24 days but were most marked between 87-126 days after treatment and persisted up to 147 days. When animals were mated 200 days after treatment, no significant changes were observed. In a parallel study, administration of 14.8 MBq/kg 114mIn resulted in decreased testis and epididymal weight and sperm reserves. Maximal reduction occurred between 87-108 days after injection followed by recovery toward control values, but neither organ had reached normal levels at 200 days. A single dose of 3.7 MBq/kg, however, had no effect on reproductive organ weight or sperm content. Male F1 progeny from the 14.8 MBq/kg group of the second mating period (commencing at 24 days) displayed decreased testis weights and sperm content and provoked a higher incidence of dominant lethal mutations. This effect was not observed in male progeny from any other time or the alternative dose level.


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