Spermatogenic and mutagenic damage after paternal exposure to systemic indium-114m.
dc.contributor.author | Hoyes, Katherine P | |
dc.contributor.author | Sharma, Harbans L | |
dc.contributor.author | Jackson, H | |
dc.contributor.author | Hendry, Jolyon H | |
dc.contributor.author | Morris, Ian D | |
dc.date.accessioned | 2010-04-09T09:14:05Z | |
dc.date.available | 2010-04-09T09:14:05Z | |
dc.date.issued | 1994-08 | |
dc.identifier.citation | Spermatogenic and mutagenic damage after paternal exposure to systemic indium-114m. 1994, 139 (2):185-93 Radiat. Res. | en |
dc.identifier.issn | 0033-7587 | |
dc.identifier.pmid | 8052694 | |
dc.identifier.uri | http://hdl.handle.net/10541/96084 | |
dc.description.abstract | The 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.iso | en | en |
dc.subject.mesh | Animals | |
dc.subject.mesh | Body Weight | |
dc.subject.mesh | Indium Radioisotopes | |
dc.subject.mesh | Infertility, Male | |
dc.subject.mesh | Litter Size | |
dc.subject.mesh | Male | |
dc.subject.mesh | Mutation | |
dc.subject.mesh | Organ Size | |
dc.subject.mesh | Radiation Dosage | |
dc.subject.mesh | Rats | |
dc.subject.mesh | Rats, Sprague-Dawley | |
dc.subject.mesh | Spermatogenesis | |
dc.subject.mesh | Testis | |
dc.title | Spermatogenic and mutagenic damage after paternal exposure to systemic indium-114m. | en |
dc.type | Article | en |
dc.contributor.department | Department of Experimental Radiation Oncology, Paterson Institute for Cancer Research, Manchester, United Kingdom. | en |
dc.identifier.journal | Radiation Research | en |
html.description.abstract | The 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. |