Maternal exposure to low dose BDE209 and Pb mixture induced neurobehavioral anomalies in C57BL/6 male offspring

被引:28
作者
Chen, Yuanhong [1 ,2 ,3 ]
Liu, Shuyun [3 ]
Xu, Hui [1 ,2 ]
Zheng, Huiying [3 ]
Bai, Chenglian [3 ]
Pan, Wenhao [3 ]
Zhou, Huanhuan [3 ]
Liao, Min [4 ]
Huang, Changjiang [3 ]
Dong, Qiaoxiang [1 ,2 ,3 ]
机构
[1] Wenzhou Med Univ, Affiliated Hosp 2, Wenzhou 325035, Peoples R China
[2] Wenzhou Med Univ, Yuying Childrens Hosp, Wenzhou 325035, Peoples R China
[3] Wenzhou Med Univ, Inst Environm Safety & Human Hlth, Wenzhou 325035, Peoples R China
[4] Wenzhou Med Univ, Sch Basic Med, Wenzhou 325035, Peoples R China
基金
中国国家自然科学基金;
关键词
Environmental pollutants; Lead; BDE209; Autism spectrum disorder; Behavioral assessment; AUTISM SPECTRUM DISORDERS; DECABROMODIPHENYL ETHER BDE-209; MORRIS WATER MAZE; HUMAN HEALTH; E-WASTE; BEHAVIORAL PHENOTYPES; SOCIAL DEFICITS; LEAD-EXPOSURE; MOUSE MODELS; CHILDREN;
D O I
10.1016/j.tox.2019.02.016
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Polybrominated diphenyl ethers (PBDEs) and lead (Pb) are common pollutants that co-exist in the environment. These chemicals may be associated with autism spectrum disorder (ASD), yet direct evidence is lacking. More importantly, how co-exposure of these chemicals might affect ASD has never been explored. For assessing the relationship between PBDE/Pb exposure and ASD, pregnant C57BL/6 J female mice were exposed to BDE209 (0.12 ng/day), Pb (1.2 ng/day), or a BDE209/Pb mixture from gestational day (GD) 9.5 to postnatal day (PND) 21 using ALZET osmotic pumps. Polyinosinic-polycytidylic acid (poly I:C) was included as a positive control, as its single dose injection (20 mg/kg.bw; i.p.) at mid-pregnancy (GD 12.5) produces ASD-like behaviors in mouse offspring. These ASD-like phenotypes include decreased preference for social novelty, increased marble burying behavior, and learning impairment. Similar to the poly I:C control, perinatal exposure to Pb or BDE209/Pb mixture elicited increased marble burying and learning impairment, but it had no effect on sociability. Consistent with these behavioral anomalies, Pb and BDE209/Pb co-exposure as well as poly I:C exposure increased the production of pro-inflammation cytokines interleukin 4 (IL-4), interleukin 6 (IL-6), interleukin 10 (IL-10), tumor necrosis factor a (TNFa), interferon y (IFNy), and interleukin 17 A (IL-17 A) in the serum, and decreased neuronal cells in the CA1 and CA3 subregions of the hippocampus. The majority of these changes in the BDE209/Pb mixture group were due to the effect of Pb rather than BDE209. However, BDE209/Pb co exposure elicited a synergistic increase in the production of IL-4, IL-6, TNFa, IFNy, and IL-17A in the serum. BDE209 exposure alone also significantly affected spatial learning and increased the production of IL-10, TNFa, and IL-17 A in the serum of male offspring. Our work demonstrates that perinatal exposure to a low dose of Pb or the BDE209/Pb mixture, although it did not induce typical ASD-like symptoms, elicited restricted, repetitive patterns of behavior and affected learning in male offspring. In addition, the synergistic increase in the systemic inflammatory response in the BDE209/Pb co-exposure group underscores the importance of evaluating chemical mixtures in disease onset.
引用
收藏
页码:70 / 80
页数:11
相关论文
共 71 条
[1]   A review of sources, levels, and toxicity of polybrominated diphenyl ethers (PBDEs) and their transformation and transport in various environmental compartments [J].
Akortia, Eric ;
Okonkwo, Jonathan O. ;
Lupankwa, Mlindelwa ;
Osae, Shiloh D. ;
Daso, Adegbenro P. ;
Olukunle, Olubiyi I. ;
Chaudhary, Abdul .
ENVIRONMENTAL REVIEWS, 2016, 24 (03) :253-273
[2]   Elevated serum levels of interleukin-17A in children with autism [J].
AL-Ayadhi, Laila Yousef ;
Mostafa, Gehan Ahmed .
JOURNAL OF NEUROINFLAMMATION, 2012, 9
[3]   Central nervous changes in social dysfunction:: Autism, aggression, and psychopathy [J].
Anckarsäter, H .
BRAIN RESEARCH BULLETIN, 2006, 69 (03) :259-265
[4]   Attention deficit hyperactivity disorder and autism spectrum disorder in children born to mothers with thyroid dysfunction: a Danish nationwide cohort study [J].
Andersen, S. L. ;
Laurberg, P. ;
Wu, C. S. ;
Olsen, J. .
BJOG-AN INTERNATIONAL JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 2014, 121 (11) :1365-1374
[5]  
[Anonymous], DEV SCI
[6]  
[Anonymous], 2019, LEAD POISONING HLTH
[7]  
[Anonymous], CURR PROTOC TOXICOL
[8]   Elevated plasma cytokines in autism spectrum disorders provide evidence of immune dysfunction and are associated with impaired behavioral outcome [J].
Ashwood, Paul ;
Krakowiak, Paula ;
Hertz-Picciotto, Irva ;
Hansen, Robin ;
Pessah, Isaac ;
Van de Water, Judy .
BRAIN BEHAVIOR AND IMMUNITY, 2011, 25 (01) :40-45
[9]   MRI volumes of amygdala and hippocampus in non-mentally retarded autistic adolescents and adults [J].
Aylward, EH ;
Minshew, NJ ;
Goldstein, G ;
Honeycutt, NA ;
Augustine, AM ;
Yates, KO ;
Barta, PE ;
Pearlson, GD .
NEUROLOGY, 1999, 53 (09) :2145-2150
[10]   Disruptive CHD8 Mutations Define a Subtype of Autism Early in Development [J].
Bernier, Raphael ;
Golzio, Christelle ;
Xiong, Bo ;
Stessman, Holly A. ;
Coe, Bradley P. ;
Penn, Osnat ;
Witherspoon, Kali ;
Gerdts, Jennifer ;
Baker, Carl ;
Vulto-van Silfhout, Anneke T. ;
Schuurs-Hoeijmakers, Janneke H. ;
Fichera, Marco ;
Bosco, Paolo ;
Buono, Serafino ;
Alberti, Antonino ;
Failla, Pinella ;
Peeters, Hilde ;
Steyaert, Jean ;
Vissers, Lisenka E. L. M. ;
Francescatto, Ludmila ;
Mefford, Heather C. ;
Rosenfeld, Jill A. ;
Bakken, Trygve ;
O'Roak, Brian J. ;
Pawlus, Matthew ;
Moon, Randall ;
Shendure, Jay ;
Amaral, David G. ;
Lein, Ed ;
Rankin, Julia ;
Romano, Corrado ;
de Vries, Bert B. A. ;
Katsanis, Nicholas ;
Eichler, Evan E. .
CELL, 2014, 158 (02) :263-276