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Prenatal nicotine exposure induces poor articular cartilage quality in female adult offspring fed a high-fat diet and the intrauterine programming mechanisms

机译:产前尼古丁暴露会导致高脂饮食的成年雌性后代关节软骨质量变差,并且子宫内编程机制

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Prenatal nicotine exposure (PNE) induces skeletal growth retardation and dyslipidemia in offspring displaying intrauterine growth retardation (IUGR). Cholesterol accumulation resulting from cholesterol efflux dysfunction may reduce the quality of articular cartilage through fetal programming. This study evaluated the quality of articular cartilage of female adult offspring fed a high-fat diet and explored the mechanisms using a rat IUGR model established by the administration of 2.0 mg/kg/d of subcutaneous nicotine from gestational days 11-20. The results demonstrated an increased OARSI (Osteoarthritis Research Society International) score and total cholesterol content, decreased serum corticosterone, and increased IGF1 and dyslipidemia with catch-up growth in PNE adult offspring. Cartilage matrix, IGF1 and cholesterol efflux pathway expression were reduced in PNE fetuses and adult offspring. Therefore, PNE induced poor articular cartilage quality in female adult offspring fed a high-fat diet via a dual programming mechanism. (C) 2016 Elsevier Inc. All rights reserved.
机译:产前尼古丁暴露(PNE)在显示宫内发育迟缓(IUGR)的后代中引起骨骼生长迟缓和血脂异常。胆固醇外排功能障碍引起的胆固醇积聚可能通过胎儿编程降低关节软骨的质量。这项研究评估了高脂饮食的成年雌性后代的关节软骨质量,并探索了使用大鼠IUGR模型的机制,该模型是在妊娠第11至20天通过给予2.0 mg / kg / d皮下烟碱建立的。结果表明,在PNE成年后代中,OARSI(国际骨关节炎研究协会国际)评分和总胆固醇含量增加,血清皮质类固醇降低,IGF1和血脂异常增加,并具有追赶性增长。 PNE胎儿和成年后代的软骨基质,IGF1和胆固醇外排途径表达降低。因此,PNE通过双重编程机制在高脂饮食的成年雌性后代中引起较差的关节软骨质量。 (C)2016 Elsevier Inc.保留所有权利。

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