Subchronic toxicity evaluation of potassium bromate in Fischer 344 rats

被引:15
作者
Dodd, Darol E. [1 ]
Layko, Debra K. [1 ]
Cantwell, Katherine E. [1 ]
Willson, Gabrielle A. [2 ]
Thomas, Russell S. [1 ]
机构
[1] Hamner Inst Hlth Sci, Res Triangle Pk, NC 27709 USA
[2] Expt Pathol Labs Inc, Res Triangle Pk, NC 27709 USA
关键词
Potassium bromate; F344; rats; Hyaline droplets; OXIDATIVE DNA-DAMAGE; CELL-PROLIFERATION; RENAL CARCINOGEN; F344; RATS; GLUTATHIONE; CYSTEINE; KIDNEYS; STRESS; MICE;
D O I
10.1016/j.etap.2013.10.005
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Male F344 rats were exposed to potassium bromate (KBrO3) in drinking water at concentrations of 0, 5, 20, 100, 200, or 400 mg/L for 2 or 13 weeks. Endpoints evaluated included clinical observations, body weights, serum chemistry, gross pathology, organ weights, and select tissue histopathology (kidney, lung, liver, thyroid, and tunica vaginalis). Weekly body weight and water consumption means were similar between KBrO3 and control groups throughout the study. Increases in kidney weights were observed in rats of the 400 mg/L group following 2- or 13-weeks exposure. Hyaline droplets were observed in renal tubules of rats of the 200 and 400 mg/L groups following 2 weeks exposure and in rats of the 400 mg/L group at 13 weeks. There were no KBrO3-related microscopic findings in the lung, liver, thyroid, and tunica vaginalis at the 2- and 13-week time points. A no observed effect level of 100 mg/L KBrO3 (8.1 mg/kg/day) was selected based on the absence of microscopic alterations in the kidney. (c) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:1227 / 1234
页数:8
相关论文
共 25 条
[1]  
American Industrial Hygiene Association (AIHA), 2013, EM RESP PLANN GUID W
[2]   Carcinogenicity of potassium bromate administered in the drinking water to male B6C3F1 mice and F344/N rats [J].
DeAngelo, AB ;
George, MH ;
Kilburn, SR ;
Moore, TM ;
Wolf, DC .
TOXICOLOGIC PATHOLOGY, 1998, 26 (05) :587-594
[3]   ACUTE CYTOGENETIC EFFECTS OF POTASSIUM BROMATE ON RAT BONE-MARROW CELLS INVIVO [J].
FUJIE, K ;
SHIMAZU, H ;
MATSUDA, M ;
SUGIYAMA, T .
MUTATION RESEARCH, 1988, 206 (04) :455-458
[4]   METABOLISM OF POTASSIUM BROMATE IN RATS .1. INVIVO STUDIES [J].
FUJII, M ;
OIKAWA, K ;
SAITO, H ;
FUKUHARA, C ;
ONOSAKA, S ;
TANAKA, K .
CHEMOSPHERE, 1984, 13 (11) :1207-1212
[5]   OZONATION OF BROMIDE-CONTAINING WATERS - KINETICS OF FORMATION OF HYPOBROMOUS ACID AND BROMATE [J].
HAAG, WR ;
HOIGNE, J .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1983, 17 (05) :261-267
[6]  
Hazardous Substance Data Bank (HSDB), 2009, 1253 HSDB
[7]   PRIMARY MUTAGENICITY SCREENING OF FOOD-ADDITIVES CURRENTLY USED IN JAPAN [J].
ISHIDATE, M ;
SOFUNI, T ;
YOSHIKAWA, K ;
HAYASHI, M ;
NOHMI, T ;
SAWADA, M ;
MATSUOKA, A .
FOOD AND CHEMICAL TOXICOLOGY, 1984, 22 (08) :623-636
[8]   ORAL-ADMINISTRATION OF THE RENAL CARCINOGEN, POTASSIUM BROMATE, SPECIFICALLY PRODUCES 8-HYDROXYDEOXYGUANOSINE IN RAT TARGET ORGAN DNA [J].
KASAI, H ;
NISHIMURA, S ;
KUROKAWA, Y ;
HAYASHI, Y .
CARCINOGENESIS, 1987, 8 (12) :1959-1961
[9]   LACK OF RENAL TUMOR-INITIATING ACTIVITY OF A SINGLE DOSE OF POTASSIUM BROMATE, A GENOTOXIC RENAL CARCINOGEN IN MALE F344/NCR RATS [J].
KURATA, Y ;
DIWAN, BA ;
WARD, JM .
FOOD AND CHEMICAL TOXICOLOGY, 1992, 30 (03) :251-259
[10]  
KUROKAWA Y, 1986, JNCI-J NATL CANCER I, V77, P977