Lejonklou Margareta H, Dunder Linda, Bladin Emelie, Pettersson Vendela, Rönn Monika, Lind Lars, Waldén Tomas B, Lind P Monica
Department of Medical Sciences, Occupational and Environmental Medicine, Uppsala University , Uppsala, Sweden.
Department of Medical Sciences, Cardiovascular Epidemiology, Uppsala University , Uppsala, Sweden.
Environ Health Perspect. 2017 Jun 28;125(6):067018. doi: 10.1289/EHP505.
Bisphenol A (BPA) is an endocrine-disrupting chemical that may contribute to development of obesity and metabolic disorders. Humans are constantly exposed to low concentrations of BPA, and studies support that the developmental period is particularly sensitive.
The aim was to investigate the effects of low-dose developmental BPA exposure on metabolic parameters in male and female Fischer 344 (F344) rat offspring.
Pregnant F344 rats were exposed to BPA via their drinking water, corresponding to 0.5 μg/kg BW/d (BPA0.5; n=21) or 50 μg/kg BW/d (BPA50; n=16), from gestational day (GD) 3.5 until postnatal day (PND) 22, and controls were given vehicle (n=26). Body weight (BW), adipose tissue, liver (weight, histology, and gene expression), heart weight, and lipid profile were investigated in the 5-wk-old offspring.
Males and females exhibited differential susceptibility to the different doses of BPA. Developmental BPA exposure increased plasma triglyceride levels (0.81±0.10 mmol/L compared with 0.57±0.03 mmol/L, females BPA50 p=0.04; 0.81±0.05 mmol/L compared with 0.61±0.04 mmol/L, males BPA0.5 p=0.005) in F344 rat offspring compared with controls. BPA exposure also increased adipocyte cell density by 122% in inguinal white adipose tissue (iWAT) of female offspring exposed to BPA0.5 compared with controls (68.2±4.4 number of adipocytes/HPF compared with 55.9±1.5 number of adipocytes/HPF; p=0.03) and by 123% in BPA0.5 females compared with BPA50 animals (68.2±4.4 number of adipocytes/high power field (HPF) compared with 55.3±2.9 number of adipocytes/HPF; p=0.04). In iWAT of male offspring, adipocyte cell density was increased by 129% in BPA50-exposed animals compared with BPA0.5-exposed animals (69.9±5.1 number of adipocytes/HPF compared with 54.0±3.4 number of adipocytes/HPF; p=0.03). Furthermore, the expression of genes involved in lipid and adipocyte homeostasis was significantly different between exposed animals and controls depending on the tissue, dose, and sex.
Developmental exposure to 0.5 μg/kg BW/d of BPA, which is 8-10 times lower than the current preliminary EFSA (European Food Safety Authority) tolerable daily intake (TDI) of 4 μg/kg BW/d and is within the range of environmentally relevant levels, was associated with sex-specific differences in the expression of genes in adipose tissue plasma triglyceride levels in males and adipocyte cell density in females when F344 rat offspring of dams exposed to BPA at 0.5 μg/kg BW/d were compared with the offspring of unexposed controls. https://doi.org/10.1289/EHP505.
双酚A(BPA)是一种内分泌干扰化学物质,可能导致肥胖和代谢紊乱的发生。人类持续暴露于低浓度的双酚A中,研究表明发育期对此尤为敏感。
本研究旨在调查低剂量双酚A发育暴露对雄性和雌性Fischer 344(F344)大鼠后代代谢参数的影响。
将怀孕的F344大鼠从妊娠第3.5天至出生后第22天通过饮用水暴露于双酚A,剂量分别为0.5 μg/kg体重/天(BPA0.5;n = 21)或50 μg/kg体重/天(BPA50;n = 16),对照组给予赋形剂(n = 26)。对5周龄后代的体重、脂肪组织、肝脏(重量、组织学和基因表达)、心脏重量和血脂谱进行了研究。
雄性和雌性对不同剂量双酚A的易感性存在差异。与对照组相比,发育期双酚A暴露增加了F344大鼠后代的血浆甘油三酯水平(雌性BPA50组为0.81±0.10 mmol/L,对照组为0.57±0.03 mmol/L,p = 0.04;雄性BPA0.5组为0.81±0.05 mmol/L,对照组为0.61±0.04 mmol/L,p = 0.005)。与对照组相比,暴露于BPA0.5的雌性后代腹股沟白色脂肪组织(iWAT)中的脂肪细胞密度增加了122%(68.2±4.4个脂肪细胞/高倍视野(HPF),对照组为55.9±1.5个脂肪细胞/HPF;p = 0.03),与BPA50组雌性相比,BPA0.5组雌性增加了123%(68.2±4.4个脂肪细胞/HPF,BPA50组为55.3±2.9个脂肪细胞/HPF;p = 0.04)。在雄性后代的iWAT中,暴露于BPA50的动物与暴露于BPA0.5的动物相比,脂肪细胞密度增加了129%(69.9±5.1个脂肪细胞/HPF,BPA0.5组为54.0±3.4个脂肪细胞/HPF;p = 0.03)。此外,根据组织、剂量和性别,暴露动物和对照动物之间参与脂质和脂肪细胞稳态的基因表达存在显著差异。
当将暴露于0.5 μg/kg体重/天双酚A的母鼠的F344大鼠后代与未暴露对照组的后代进行比较时,发育期暴露于0.5 μg/kg体重/天的双酚A(比欧洲食品安全局(EFSA)目前初步确定的4 μg/kg体重/天的每日可耐受摄入量(TDI)低8 - 10倍,且在环境相关水平范围内)与雄性脂肪组织中基因表达、血浆甘油三酯水平以及雌性脂肪细胞密度的性别特异性差异有关。https://doi.org/10.1289/EHP505