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慢性暴露于无铅汽油或2,2,4-三甲基戊烷期间,F344大鼠近端肾小管细胞增殖增加及α2u-球蛋白蓄积的定位。

Elevated proliferation of proximal tubule cells and localization of accumulated alpha 2u-globulin in F344 rats during chronic exposure to unleaded gasoline or 2,2,4-trimethylpentane.

作者信息

Short B G, Burnett V L, Swenberg J A

机构信息

Department of Biochemical Toxicology and Pathobiology, Chemical Industry Institute of Toxicology, Research Triangle Park, North Carolina 27709.

出版信息

Toxicol Appl Pharmacol. 1989 Dec;101(3):414-31. doi: 10.1016/0041-008x(89)90191-9.

Abstract

In order to better characterize the pathogenesis of alpha 2u-globulin (alpha 2uG) nephropathy, cell proliferation was quantitated within the three proximal tubule segments of the kidney (P1, P2, and P3) and proximal tubule segments affected by chronic progressive nephrosis (CPN) in male and female F344 rats exposed to 10, 70, or 300 ppm unleaded gasoline (UG) or 50 ppm 2,2,4-trimethylpentane (TMP) from 3 to 50 weeks. The P2 segment of male rats exposed to UG or TMP responded with dose-related increases in cell turnover (up to 11-fold) that persisted during chronic exposure. This proliferative response closely paralleled the extent and severity of immunohistochemically detectable alpha 2uG in the P2 segment. Neither alpha 2uG nor cytotoxicity was evident in cells of the P1 or P3 segment; however, cell proliferation was increased (up to 8-fold) for up to 22 weeks of exposure in the P3 segment. Increased numbers of proximal tubules affected by CPN were found in males exposed to UG or TMP for 22 or 48 weeks, compared to controls. These lesions contained epithelial cells that were highly proliferative. Control or treated female rats exhibited neither alpha 2uG nephropathy nor increases in P2 or P3 cell turnover, and the extent of CPN was greatly reduced as compared to male rats. The results of this and related studies suggest that chronic cell proliferation associated with alpha 2uG nephropathy and CPN in male rats exposed to UG or isoparaffinic components of UG, such as TMP, may be responsible for the sex- and species-specific nephrocarcinogenic effects of UG.

摘要

为了更好地描述α2u球蛋白(α2uG)肾病的发病机制,对雄性和雌性F344大鼠从3周龄至50周龄暴露于10、70或300 ppm无铅汽油(UG)或50 ppm 2,2,4-三甲基戊烷(TMP)后,肾脏的三个近端小管节段(P1、P2和P3)以及受慢性进行性肾病(CPN)影响的近端小管节段内的细胞增殖进行了定量分析。暴露于UG或TMP的雄性大鼠的P2节段出现与剂量相关的细胞更新增加(高达11倍),在慢性暴露期间持续存在。这种增殖反应与P2节段中免疫组化可检测到的α2uG的程度和严重程度密切平行。在P1或P3节段的细胞中,α2uG和细胞毒性均不明显;然而,在P3节段暴露长达22周时,细胞增殖增加(高达8倍)。与对照组相比,暴露于UG或TMP 22周或48周的雄性大鼠中,受CPN影响的近端小管数量增加。这些病变包含高度增殖的上皮细胞。对照或经处理的雌性大鼠既未表现出α2uG肾病,P2或P3细胞更新也未增加,并且与雄性大鼠相比,CPN的程度大大降低。这项研究及相关研究的结果表明,暴露于UG或UG的异链烷烃成分(如TMP)的雄性大鼠中,与α2uG肾病和CPN相关的慢性细胞增殖可能是UG性别和物种特异性肾致癌作用的原因。

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