Joly Condette Claire, Bach Véronique, Mayeur Camille, Gay-Quéheillard Jérôme, Khorsi-Cauet Hafida
*Peritox Laboratory, EA4285 UMI01 INERIS, Faculty of Medicine, Jules Verne University of Picardy, Amiens †Commensal and Probiotics-Host Interactions Laboratory, INRA, UMR 1319 MICALIS, Jouy-en-Josas, France.
J Pediatr Gastroenterol Nutr. 2015 Jul;61(1):30-40. doi: 10.1097/MPG.0000000000000734.
Pesticide exposure via residues in food may be especially harmful when it takes place in the developing child. The present study was designed to assess the impact of perinatal exposure to chlorpyrifos (CPF, an insecticide known to cross the placental barrier).
Female rats were exposed to oral CPF (1 or 5 mg kg day vs vehicle controls) from gestation onset up to weaning of the pups that were individually gavaged (CPF or vehicle) thereafter. Two developmental time points were studied: weaning (day 21) and adulthood (day 60). After sacrifice, samples from the intestinal tract and other organs underwent microbiological and histological analyses.
Rat pups exposed to 5 mg kg day CPF were both significantly smaller (body length) and lighter than controls. Exposure to CPF was associated with changes in the histological structures (shorter and thinner intestinal villosities), an intestinal microbial dysbiosis, and increased bacterial translocation in the spleen and liver. These significant microbial changes in the gut were associated with impaired epithelium protection (mucin-2) and microbial pattern recognition receptor (Toll-like 2 and 4) gene expression.
Exposure to CPF during gestation and development affected the pups' intestinal development, with morphological alteration of the structures involved in nutrient absorption, intestinal microbial dysbiosis, alteration of mucosal barrier (mucin-2), stimulation of the innate immune system, and increased bacterial translocation. Perinatal exposure to CPF may therefore have short- and long-term impacts on the digestive tract.
通过食物中的残留农药接触农药,对于发育中的儿童可能特别有害。本研究旨在评估围产期接触毒死蜱(CPF,一种已知可穿过胎盘屏障的杀虫剂)的影响。
从妊娠开始至幼崽断奶,雌性大鼠口服CPF(1或5毫克/千克/天,与溶剂对照组相比),此后对幼崽单独灌胃(CPF或溶剂)。研究了两个发育时间点:断奶期(第21天)和成年期(第60天)。处死后,对肠道和其他器官的样本进行微生物学和组织学分析。
暴露于5毫克/千克/天CPF的幼鼠体型(体长)明显小于对照组,体重也更轻。接触CPF与组织结构变化(肠绒毛更短更细)、肠道微生物失调以及脾脏和肝脏中细菌易位增加有关。肠道中这些显著的微生物变化与上皮保护(粘蛋白-2)受损和微生物模式识别受体(Toll样受体2和4)基因表达改变有关。
在妊娠和发育期间接触CPF会影响幼鼠的肠道发育,导致参与营养吸收的结构形态改变、肠道微生物失调、粘膜屏障(粘蛋白-2)改变、先天免疫系统受到刺激以及细菌易位增加。因此,围产期接触CPF可能对消化道产生短期和长期影响。