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在四氢呋喃 2 年吸入致癌性研究中雄性 F344 大鼠肾脏的组织病理学变化:病理学工作组的回顾和再评估。

Histopathologic changes in the kidneys of male F344 rats from a 2-year inhalation carcinogenicity study of tetrahydrofuran: a pathology working group review and re-evaluation.

机构信息

Biotechnics Inc, 401 Augusta Rd, Clemson, SC 29631, USA.

出版信息

Regul Toxicol Pharmacol. 2010 Oct;58(1):100-5. doi: 10.1016/j.yrtph.2010.04.009. Epub 2010 May 4.

Abstract

Risk evaluation and hazard classification for tetrahydrofuran (THF) is based partly on the incidences of renal tumors in male F344/N rats reported in a 2-year carcinogenicity study by the National Toxicology Program (NTP). A Pathology Working Group (PWG) was commissioned to conduct an independent review of the kidney slides from this bioassay (along with two subchronic studies) to assess renal changes in light of recent scientific work on pathogenesis of pre-neoplastic and neoplastic lesions in rat kidney. PWG pathologists confirmed the NTP assessment that adenomas were non-statistically increased in animals exposed to the highest level of THF. However, when pre-neoplastic and neoplastic lesions were combined, there was no difference between control and THF-exposed groups. Also, the majority of these proliferative lesions were in rats with severe chronic progressive nephropathy (CPN). Accordingly, the PWG concluded that renal lesions in the control and THF-exposed groups resulted primarily from regenerative processes associated with advanced CPN. Based on an alpha(2u)-globulin/hyaline droplet response observed in a 4-week study with THF, the PWG could not exclude the possibility of both advanced CPN and low-grade alpha2u-g nephropathy contributing to the renal proliferative lesions developing chronically in high-dose males. Neither condition has a pathologic counterpart in humans.

摘要

四氢呋喃(THF)的风险评估和危害分类部分基于国家毒理学计划(NTP)进行的为期 2 年的致癌性研究中雄性 F344/N 大鼠肾脏肿瘤发生率的报告。一个病理学工作组(PWG)受委托对该生物测定(以及两项亚慢性研究)的肾脏切片进行独立审查,以根据最近关于大鼠肾脏前瘤性和瘤性病变发病机制的科学工作来评估肾脏变化。PWG 病理学家证实 NTP 的评估,即暴露于最高水平 THF 的动物的腺瘤非统计学上增加。然而,当将前瘤性和瘤性病变结合起来时,对照组和 THF 暴露组之间没有差异。此外,这些增生性病变中的大多数发生在患有严重慢性进行性肾病(CPN)的大鼠中。因此,PWG 得出结论,对照组和 THF 暴露组的肾脏病变主要是由与晚期 CPN 相关的再生过程引起的。基于 THF 进行的为期 4 周研究中观察到的α2u-球蛋白/透明滴反应,PWG 不能排除晚期 CPN 和低级别α2u-g 肾病都可能导致高剂量雄性大鼠慢性发展的肾脏增生性病变的可能性。这两种情况在人类中都没有相应的病理表现。

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