Dose and time relationships in the endocrine response of the irradiated adult rat testis.
dc.contributor.author | Delic, Julian I | |
dc.contributor.author | Hendry, Jolyon H | |
dc.contributor.author | Morris, Ian D | |
dc.contributor.author | Shalet, Stephen M | |
dc.date.accessioned | 2010-12-03T16:51:47Z | |
dc.date.available | 2010-12-03T16:51:47Z | |
dc.date.issued | 1986 | |
dc.identifier.citation | Dose and time relationships in the endocrine response of the irradiated adult rat testis., 7 (1):32-41 J Androl | en |
dc.identifier.issn | 0196-3635 | |
dc.identifier.pmid | 3003018 | |
dc.identifier.uri | http://hdl.handle.net/10541/117157 | |
dc.description.abstract | The dose- and time-dependent responses for the interstitial and tubular compartments in irradiated adult rat testes are described. Leydig cell dysfunction, as indicated by increased serum LH (to a maximum of 385% of control after 5 Gy) and decreased serum T (to a minimum of 30% of control after 10 Gy), was observed at 8 weeks postirradiation. Subsequent recovery of Leydig cell function was then observed, so that after 9 months serum T was normal but LH was still marginally elevated. The dysfunction, with a threshold of about 4 to 5 Gy, was associated with a loss of Leydig cells from the testis. Spermatogenic damage was observed; after doses of 3 Gy and above a marked dose-response was recorded as assessed by counts of tubule cross sections exhibiting spermatogenesis. Reduced serum levels of androgen binding protein indicated Sertoli cell dysfunction at 8 weeks after 3 Gy and above, with values of less than one half of those seen in the controls. Serum FSH also was elevated to between 150% and 200% of control, and after 9 months closely reflected androgen binding protein changes. Unlike the Leydig cell, no recovery with time was observed for this aspect of Sertoli cell function. | |
dc.language.iso | en | en |
dc.subject.mesh | Androgen-Binding Protein | |
dc.subject.mesh | Animals | |
dc.subject.mesh | Dose-Response Relationship, Radiation | |
dc.subject.mesh | Follicle Stimulating Hormone | |
dc.subject.mesh | Kinetics | |
dc.subject.mesh | Leydig Cells | |
dc.subject.mesh | Luteinizing Hormone | |
dc.subject.mesh | Male | |
dc.subject.mesh | Organ Size | |
dc.subject.mesh | Radiation Injuries | |
dc.subject.mesh | Rats | |
dc.subject.mesh | Rats, Inbred Strains | |
dc.subject.mesh | Receptors, Cell Surface | |
dc.subject.mesh | Receptors, LH | |
dc.subject.mesh | Regeneration | |
dc.subject.mesh | Seminiferous Tubules | |
dc.subject.mesh | Testicular Diseases | |
dc.subject.mesh | Testosterone | |
dc.title | Dose and time relationships in the endocrine response of the irradiated adult rat testis. | en |
dc.type | Article | en |
dc.contributor.department | Paterson Laboratories, Christie Hospital and Holt Radium Institute, Manchester, M20 9BX, UK. | en |
dc.identifier.journal | Journal of Andrology | en |
html.description.abstract | The dose- and time-dependent responses for the interstitial and tubular compartments in irradiated adult rat testes are described. Leydig cell dysfunction, as indicated by increased serum LH (to a maximum of 385% of control after 5 Gy) and decreased serum T (to a minimum of 30% of control after 10 Gy), was observed at 8 weeks postirradiation. Subsequent recovery of Leydig cell function was then observed, so that after 9 months serum T was normal but LH was still marginally elevated. The dysfunction, with a threshold of about 4 to 5 Gy, was associated with a loss of Leydig cells from the testis. Spermatogenic damage was observed; after doses of 3 Gy and above a marked dose-response was recorded as assessed by counts of tubule cross sections exhibiting spermatogenesis. Reduced serum levels of androgen binding protein indicated Sertoli cell dysfunction at 8 weeks after 3 Gy and above, with values of less than one half of those seen in the controls. Serum FSH also was elevated to between 150% and 200% of control, and after 9 months closely reflected androgen binding protein changes. Unlike the Leydig cell, no recovery with time was observed for this aspect of Sertoli cell function. |