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无处不在的塑化剂邻苯二甲酸二(2-乙基己基)酯增强自闭症儿童单核细胞的现有炎症特征。

Ubiquitous plasticizer, Di-(2-ethylhexyl) phthalate enhances existing inflammatory profile in monocytes of children with autism.

机构信息

Department of Pharmacology and Toxicology, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.

Department of Pharmacology and Toxicology, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.

出版信息

Toxicology. 2020 Dec 15;446:152597. doi: 10.1016/j.tox.2020.152597. Epub 2020 Sep 28.

Abstract

Genetic as well as environmental factors are believed to play a significant role in the pathogenesis and progression of autism spectrum disorder (ASD). Phthalates are ubiquitous environmental contaminants as they are used plasticizers in several household/industrial products such as vinyl flooring, plastic toys, and cosmetic products. One of the plasticizers that is quite prevalent in these products is di-2-ethylhexyl phthalate (DEHP) which can cause human exposure via dermal/inhalation/ingestion routes. DEHP and its metabolites are associated with behavioral dysregulations and reported to be increased in systemic circulation of ASD children. DEHP is reported to cause upregulation of several inflammatory cytokines in different cells/tissues, however its role in inflammatory signaling of ASD monocytes has not been investigated earlier. Therefore, this study evaluated the effects of DEHP (at 5 μM final concentration for 24 h) on inflammatory profile (NFkB, STAT3, IL-6, TNF-α, IL-1β) in monocytes of ASD subjects and typically developing control (TDC) children. Our data show that DEHP upregulates NFkB/STAT3 expression which is associated with increased inflammatory profile in monocytes of ASD and TDC subjects, however its effect is much greater in magnitude in the former group. This was confirmed by utilization of NFkB inhibitor, PDTC and STAT3 inhibitor, Stattic which caused reduction in inflammatory cytokines from DEHP-treated monocytes in ASD group. In short, DEHP causes further elevation in inflammatory signaling in ASD monocytes which could be due to existing inflammation in this group. These data suggest that use of plasticizers such as DEHP should be minimized in order to avoid their potential effects on immune dysfunction associated with ASD.

摘要

遗传和环境因素被认为在自闭症谱系障碍 (ASD) 的发病机制和进展中起重要作用。邻苯二甲酸酯是普遍存在的环境污染物,因为它们被用作几种家庭/工业产品的增塑剂,如乙烯基地板、塑料玩具和化妆品。这些产品中相当普遍的一种增塑剂是邻苯二甲酸二(2-乙基己基)酯 (DEHP),它可以通过皮肤/吸入/摄入途径导致人类暴露。DEHP 及其代谢物与行为失调有关,并据报道在 ASD 儿童的全身循环中增加。据报道,DEHP 会导致不同细胞/组织中几种炎症细胞因子的上调,但它在 ASD 单核细胞炎症信号中的作用尚未被研究。因此,本研究评估了 DEHP(最终浓度为 5 μM,作用 24 小时)对 ASD 患者和典型发育对照 (TDC) 儿童单核细胞炎症谱(NFkB、STAT3、IL-6、TNF-α、IL-1β)的影响。我们的数据表明,DEHP 上调 NFkB/STAT3 表达,这与 ASD 和 TDC 受试者单核细胞炎症谱增加有关,但在前者中的作用更大。这一点通过使用 NFkB 抑制剂 PDTC 和 STAT3 抑制剂 Stattic 得到了证实,它们导致 ASD 组中 DEHP 处理的单核细胞中炎症细胞因子减少。简而言之,DEHP 导致 ASD 单核细胞中炎症信号进一步升高,这可能是由于该组存在炎症。这些数据表明,应尽量减少使用 DEHP 等增塑剂,以避免其对与 ASD 相关的免疫功能障碍的潜在影响。

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