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在大鼠模型中,暴露于环境污染物和补充叶酸会通过父系在代际间影响胎儿骨骼发育。

Exposure to environmental contaminants and folic acid supplementation intergenerationally impact fetal skeleton development through the paternal lineage in a rat model.

作者信息

L Charest Phanie, Tessougue Emmanuel, Lessard Maryse, Herst Pauline M, Navarro Pauline, Kimmins Sarah, Trasler Jacquetta M, MacFarlane Amanda J, Benoit-Biancamano Marie-Odile, Bailey Janice L, Dalvai Mathieu

机构信息

Department of Animal Sciences, Faculty of Agricultural and Food Sciences, Université Laval, Quebec City, QC, Canada.

Centre de Recherche en Reproduction Développement et Santé Intergénérationnelle (CRDSI), Université Laval, Quebec City, QC, Canada.

出版信息

Front Toxicol. 2022 Sep 27;4:881622. doi: 10.3389/ftox.2022.881622. eCollection 2022.

DOI:10.3389/ftox.2022.881622
PMID:36238601
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9552329/
Abstract

Persistent organic pollutants (POPs) are ubiquitous in the environment, which is of concern since they are broadly toxic for wildlife and human health. It is generally accepted that maternal prenatal folic acid supplementation (FA) may beneficially impact offspring development, but it has been recently shown that the father's exposures also influence the health of his offspring. Bone is an endocrine organ essential for whole-body homeostasis and is susceptible to toxicants. Herein, we tested the hypotheses that prenatal paternal exposure to POPs induces developmental bone disorders in fetuses across multiple generations and that FA supplementation attenuates these disorders. We used a four-generation rat model, in which F0 founder females were divided into four treatment groups. F0 females were gavaged with corn oil or an environmentally-relevant POPs mixture and fed either a control diet (2 mg FA/kg), or FA supplemented diet (6 mg FA/kg) before mating and until parturition (four treatments in total). After the birth of the F1 litters, all F0 females and subsequent generations received the FA control diet. Staining with alcian blue and alizarin red S of male and female fetal skeletons was performed at Gestational Day 19.5. Paternal direct and ancestral exposure to POPs delayed bone ossification and decreased the length of long limb bones in fetuses. Maternal FA supplementation did not counteract the POPs-associated delayed fetal ossification and reduced long bone length. In conclusion, prenatal paternal POPs exposure causes developmental bone abnormalities over multiple generations, which were not corrected by maternal FA supplementation.

摘要

持久性有机污染物(POPs)在环境中无处不在,鉴于它们对野生动物和人类健康具有广泛毒性,这令人担忧。人们普遍认为,母亲在孕期补充叶酸(FA)可能对后代发育有益,但最近研究表明,父亲的接触也会影响其后代的健康。骨骼是维持全身稳态所必需的内分泌器官,且易受毒物影响。在此,我们检验了以下假设:产前父体接触POPs会在多代胎儿中诱发发育性骨骼疾病,而补充FA可减轻这些疾病。我们使用了四代大鼠模型,其中F0代奠基雌性大鼠被分为四个处理组。F0代雌性大鼠在交配前直至分娩期间,通过灌胃给予玉米油或与环境相关的POPs混合物,并分别喂食对照饮食(2毫克FA/千克)或补充FA的饮食(6毫克FA/千克)(总共四种处理)。F1代幼崽出生后,所有F0代雌性大鼠及其后代均接受FA对照饮食。在妊娠第19.5天,对雄性和雌性胎儿骨骼进行阿尔辛蓝和茜素红S染色。父体直接和祖辈接触POPs会延迟胎儿骨骼骨化,并缩短胎儿四肢长骨的长度。母体补充FA并不能抵消与POPs相关的胎儿骨化延迟和长骨长度缩短。总之,产前父体接触POPs会在多代中导致发育性骨骼异常,而母体补充FA并不能纠正这些异常。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/193b/9552329/8809fdfd3e75/ftox-04-881622-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/193b/9552329/df0b25b51a95/ftox-04-881622-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/193b/9552329/3337e156ebba/ftox-04-881622-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/193b/9552329/6f04b8dc247e/ftox-04-881622-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/193b/9552329/8809fdfd3e75/ftox-04-881622-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/193b/9552329/df0b25b51a95/ftox-04-881622-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/193b/9552329/3337e156ebba/ftox-04-881622-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/193b/9552329/6f04b8dc247e/ftox-04-881622-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/193b/9552329/8809fdfd3e75/ftox-04-881622-g004.jpg

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本文引用的文献

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2
Perinatal oral exposure to low doses of bisphenol A, S or F impairs immune functions at intestinal and systemic levels in female offspring mice.围产期口腔接触低剂量双酚 A、S 或 F 会损害雌性子代小鼠肠道和全身的免疫功能。
Environ Health. 2020 Aug 31;19(1):93. doi: 10.1186/s12940-020-00614-w.
3
Perinatal low-dose PBDE-47 exposure hampered thyroglobulin turnover and induced thyroid cell apoptosis by triggering ER stress and lysosomal destabilization contributing to thyroid toxicity in adult female rats.
围产期低剂量 PBDE-47 暴露通过触发内质网应激和溶酶体不稳定,阻碍甲状腺球蛋白的转化并诱导甲状腺细胞凋亡,导致成年雌性大鼠的甲状腺毒性。
J Hazard Mater. 2020 Jun 15;392:122265. doi: 10.1016/j.jhazmat.2020.122265. Epub 2020 Feb 10.
4
Folic acid supplementation reduces multigenerational sperm miRNA perturbation induced by environmental contaminant exposure.补充叶酸可减少环境污染物暴露引起的多代精子miRNA紊乱。
Environ Epigenet. 2019 Dec 14;5(4):dvz024. doi: 10.1093/eep/dvz024. eCollection 2019 Oct.
5
Prenatal Exposure to Environmentally-Relevant Contaminants Perturbs Male Reproductive Parameters Across Multiple Generations that are Partially Protected by Folic Acid Supplementation.环境相关污染物的产前暴露会扰乱多个世代雄性生殖参数,而叶酸补充可部分保护这些参数。
Sci Rep. 2019 Sep 25;9(1):13829. doi: 10.1038/s41598-019-50060-z.
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