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关于甲醛致癌作用与大鼠鼻腔病理学及人类健康风险评估的简要综述。

A brief review of formaldehyde carcinogenesis in relation to rat nasal pathology and human health risk assessment.

作者信息

Morgan K T

机构信息

CIIT, Research Triangle Park, North Carolina 27709, USA.

出版信息

Toxicol Pathol. 1997 May-Jun;25(3):291-307. doi: 10.1177/019262339702500307.

Abstract

The 1980 report that inhaled formaldehyde induced nasal squamous cell carcinomas in rats had a significant societal impact and resulted in extensive research in the fields of rodent nasal pathology and human cancer risk assessment. This article presents an overview of the evolution of these events. It is concluded that the nasal passages of humans and rats are fundamentally identical biological target organs. Nevertheless, in the case of human health risk assessment, minor differences between these species may be critically important. Special attention should be paid to interspecies differences in nasal dosimetry and local metabolism; thus, chemical toxicity data derived from rats require careful interpretation when used for human risk assessments. In the case of formaldehyde, it is recommended that low-concentration (< or = 2 ppm airborne exposure) extrapolation, where no tissue damage is observed, be uncoupled from the responses at high concentrations (> or = 6 ppm), where epithelial degeneration, regenerative cell replication, and inflammation appear to be essential driving forces in formaldehyde carcinogenesis. The presence of treatment-related nasal lesions in rats following exposure to chemicals should always be treated as an indication of a potential human health risk, whether exposure is by the inhalation, oral, or dermal route.

摘要

1980年关于吸入甲醛可诱发大鼠鼻腔鳞状细胞癌的报告产生了重大的社会影响,并引发了在啮齿动物鼻腔病理学和人类癌症风险评估领域的广泛研究。本文概述了这些事件的发展历程。得出的结论是,人类和大鼠的鼻腔是基本相同的生物靶器官。然而,在人类健康风险评估中,这些物种之间的细微差异可能至关重要。应特别关注鼻腔剂量学和局部代谢方面的种间差异;因此,当将大鼠的化学毒性数据用于人类风险评估时,需要仔细解读。就甲醛而言,建议将未观察到组织损伤的低浓度(≤2 ppm空气暴露)外推与高浓度(≥6 ppm)时的反应区分开来,在高浓度下,上皮变性、再生细胞复制和炎症似乎是甲醛致癌作用的重要驱动力。无论化学物质是通过吸入、口服还是皮肤途径接触,大鼠接触化学物质后出现与治疗相关的鼻腔病变都应始终被视为潜在人类健康风险的指标。

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