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首页> 外文期刊>Regulatory Toxicology and Pharmacology: RTP >Histopathology re-examination of the NTP toxicity/carcinogenicity studies of tert-butyl alcohol to identify renal tumor and toxicity modes of action
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Histopathology re-examination of the NTP toxicity/carcinogenicity studies of tert-butyl alcohol to identify renal tumor and toxicity modes of action

机译:组织病理学重新检查叔丁醇的NTP毒性/致癌性研究,以鉴定肾肿瘤和毒性作用

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摘要

Tert-butyl alcohol (TBA) targets the rat kidney following repeated exposures, including renal tubule tumors. The mode of action (MOA) of these tumors, concluded by a pathology working group, involves both alpha2u-globulin nephropathy (alpha 2u-gN) and exacerbated chronic progressive nephropathy (CPN), but has been disputed and an undefined MOA proposed. This study further reviews the histology slides of male and female rat kidneys from the NTP drinking water 13-week toxicity and 2-year carcinogenicity studies, including the 15-month interim sacrifice group. The papillary epithelial lining alteration formerly referred to as "transitional cell hyperplasia" develops as part of advanced CPN and does not represent a separate toxicity. No changes were observed in the kidney pelvis urothelium. The only alterations in subchronic male rats involved alpha 2u-gN and CPN, without test article-related alterations in females. Focused examination of areas of parenchyma unaffected by CPN in TBA-treated male and female rats of the chronic studies revealed no renal tubule abnormalities other than from the effects of alpha 2u-gN and CPN. Unrelated to toxicity were spontaneous amphophilic or vacuolar tubule proliferative lesions. All observed TBA-associated non-neoplastic and neoplastic histopathological changes in the kidney can be explained by alpha 2u-gN or enhanced CPN, neither of which are relevant to humans.
机译:叔丁醇(TBA)靶向大鼠肾,后再曝光,包括肾小管肿瘤。通过病理学工作组结束的这些肿瘤的作用方式(MOA)涉及α2u-球蛋白肾病(Alpha 2u-Gn)和加剧慢性慢性肾病(CPN),但已经提出了争议和未定义的MOA。本研究进一步评论了来自NTP饮用水13周毒性和2年致癌性研究的男性和女大鼠肾脏的组织学幻灯片,包括15个月的临时牺牲组。以前称为“过渡细胞增生”的乳头上皮衬里改变作为高级CPN的一部分,并且不代表单独的毒性。肾盂尿溶质中没有观察到任何变化。次级雄性大鼠唯一的改变涉及阿尔法2U-GN和CPN,没有测试与女性的文章相关的改变。 CPN在慢性研究的TBA治疗的雄性和女性大鼠中未受CPN不受影响的疗法检查的重点检查揭示了除了α2U-GN和CPN的影响之外的肾小管异常。与毒性无关是自发的递液或真空小管增殖性病变。所有观察到的TBA相关的非肿瘤和肿瘤组织病理学和肿瘤组织病理学变化可以通过α2U-GN或增强的CPN解释,既不是与人类相关的。

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