pubmed-article:11349434 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:11349434 | lifeskim:mentions | umls-concept:C0024554 | lld:lifeskim |
pubmed-article:11349434 | lifeskim:mentions | umls-concept:C0043227 | lld:lifeskim |
pubmed-article:11349434 | lifeskim:mentions | umls-concept:C0034693 | lld:lifeskim |
pubmed-article:11349434 | lifeskim:mentions | umls-concept:C0178784 | lld:lifeskim |
pubmed-article:11349434 | lifeskim:mentions | umls-concept:C0205070 | lld:lifeskim |
pubmed-article:11349434 | lifeskim:mentions | umls-concept:C0405581 | lld:lifeskim |
pubmed-article:11349434 | lifeskim:mentions | umls-concept:C0178602 | lld:lifeskim |
pubmed-article:11349434 | lifeskim:mentions | umls-concept:C0205341 | lld:lifeskim |
pubmed-article:11349434 | lifeskim:mentions | umls-concept:C0600688 | lld:lifeskim |
pubmed-article:11349434 | lifeskim:mentions | umls-concept:C0220825 | lld:lifeskim |
pubmed-article:11349434 | lifeskim:mentions | umls-concept:C0748342 | lld:lifeskim |
pubmed-article:11349434 | lifeskim:mentions | umls-concept:C1441672 | lld:lifeskim |
pubmed-article:11349434 | lifeskim:mentions | umls-concept:C0282116 | lld:lifeskim |
pubmed-article:11349434 | lifeskim:mentions | umls-concept:C0013125 | lld:lifeskim |
pubmed-article:11349434 | lifeskim:mentions | umls-concept:C2603343 | lld:lifeskim |
pubmed-article:11349434 | lifeskim:mentions | umls-concept:C0205171 | lld:lifeskim |
pubmed-article:11349434 | lifeskim:mentions | umls-concept:C1442465 | lld:lifeskim |
pubmed-article:11349434 | lifeskim:mentions | umls-concept:C0085752 | lld:lifeskim |
pubmed-article:11349434 | pubmed:dateCreated | 2001-5-14 | lld:pubmed |
pubmed-article:11349434 | pubmed:abstractText | The present study was performed to clarify whether toxic effects of the antitumor drug, adriamycin (ADR) on the male genital organ can be adequately detected 2 and 4 weeks after a single intravenous administration in the rat. ADR was intravenously administered once to 10 Crj:CD (SD) male rats/group aged 6 weeks (4-week group) and 8 weeks (2-week group) at doses of 0, 2 and 6 mg/kg. The rats were sacrificed at the age of 10 weeks. For comparison 10 rats/group were killed 2 weeks after a single intravenous administration at the age of 4 weeks (immature group). Saline was administered to control rats. Histopathological examination and a quantitative morphometry were carried out after measurement of testes weights at necropsy. In rats of the 4-week and 2-week groups, mean absolute testicular weight in all groups was significantly decreased. However, changes in mean relative weight were not evident in the 2-week group. Disappearance of seminiferous epithelial cells was observed histopathologically in rats dosed with 2 and 6 mg/kg in the 2-week group. The change was more severe in the 4-week group, when reduction of spermatogenesis and giant cells were also observed at 6 mg/kg. The quantitative morphometry in the 2-week group showed decreases in the numbers of spermatogonia and spermatocytes in stages X and XII at 2 mg/kg, and in the numbers of spermatogonia in all stages and spermatocytes in all stages except stage V at 6 mg/kg. Moreover, the numbers of spermatogonia and spermatocytes in all stages and spermatids in stages II-III and V were decreased with dose related manner in the 4-week group. In contrast, no obvious change in testes weights was apparent in the immature group. However, the numbers of spermatogonia and spermatocytes in all stages were decreased at 6 mg/kg. In conclusion, testicular toxicity of ADR could be detected 2 weeks after a single administration. Susceptibility of the testes of immature rats to ADR might be less than that of older animals. | lld:pubmed |
pubmed-article:11349434 | pubmed:language | eng | lld:pubmed |
pubmed-article:11349434 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11349434 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:11349434 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11349434 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11349434 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:11349434 | pubmed:month | Oct | lld:pubmed |
pubmed-article:11349434 | pubmed:issn | 0388-1350 | lld:pubmed |
pubmed-article:11349434 | pubmed:author | pubmed-author:KatsukiSS | lld:pubmed |
pubmed-article:11349434 | pubmed:author | pubmed-author:KawachiMM | lld:pubmed |
pubmed-article:11349434 | pubmed:author | pubmed-author:TsunenariII | lld:pubmed |
pubmed-article:11349434 | pubmed:author | pubmed-author:MatsumaruTT | lld:pubmed |
pubmed-article:11349434 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:11349434 | pubmed:volume | 25 Spec No | lld:pubmed |
pubmed-article:11349434 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:11349434 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:11349434 | pubmed:pagination | 103-15 | lld:pubmed |
pubmed-article:11349434 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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pubmed-article:11349434 | pubmed:year | 2000 | lld:pubmed |
pubmed-article:11349434 | pubmed:articleTitle | Collaborative work to evaluate toxicity on male reproductive organs by repeated dose studies in rats 10). Testicular toxicity of adriamycin observed 2 and 4 weeks after a single intravenous administration. | lld:pubmed |
pubmed-article:11349434 | pubmed:affiliation | Department of Toxicology & Safety Assessment, Kawanishi Pharma Research Institute, Nippon Boehringer Ingelheim Co., Ltd., 3-10-1 Yato, Kawanishi, Hyogo 666-0193, Japan. | lld:pubmed |
pubmed-article:11349434 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:11349434 | pubmed:publicationType | Comparative Study | lld:pubmed |