Triphenyl phosphate induces lipid metabolism disorder and promotes obesity through PI3K/AKT signaling pathway

IF 9.7 1区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Environment International Pub Date : 2025-04-01 DOI:10.1016/j.envint.2025.109428
Tianlan Li , Yiwa Liu , Jingyi Cao, Xianzhu Lu, Yinghan Lu, Yuhan Wang, Chunmei Zhang, Meifen Wu, Song Deng, Li Li, Ming Shi
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Abstract

Triphenyl phosphate (TPHP) is a widely used organic phosphate flame retardant that has been reported as a potential environmental obesogen. However, the potential impact and mechanism of action of TPHP on adipose tissue are still unclear. This study investigates the potential impact of TPHP on lipid metabolism disorders through in vivo and in vitro experiments. Male and female BALB/c mice were exposed to TPHP (0, 1, 10, and 150 mg/kg/day) for 60 days, and 3T3-L1 preadipocytes were treated with concentrations of TPHP (0, 0.1, 1, 10 μM) during differentiation. The results showed that exposure to TPHP could cause gender specific dyslipidemia, with male mice exhibiting dose-dependent increases in inguinal adipose tissue coefficient, adipocyte hypertrophy, and upregulation of adipose differentiation and adipogenesis-related genes. In contrast, female mice did not show significant changes in tissue morphology. This suggested that TPHP might promote the potential occurrence of adiposity by disrupting the lipid metabolism homeostasis of male adipose tissue. During the differentiation and maturation process of 3T3-L1 preadipocytes, exposure to TPHP led to increased lipid accumulation and disrupted lipid homeostasis by simultaneous activation adipogenesis and lipolysis. Multiple omics data showed that the activation of the peroxisome proliferator-activated receptor γ (PPARγ) signaling pathway and fatty acid metabolism was the core mechanism of TPHP induced metabolic dysfunction. Further research showed that TPHP activated the PI3K/AKT pathway, and PI3K inhibitor (LY294002) could rescue TPHP induced lipid droplet formation and normalize the expression of adipogenic markers. These findings confirm that TPHP is a potential environmental obesogen that can disrupt the metabolic homeostasis of white adipose tissue through the PPARγ and PI3K/AKT signaling pathways, with higher susceptibility in males. This study provides compelling evidence for the obesogenic effects of TPHP and information for risk assessment of organophosphorus flame retardants.

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磷酸三苯酯通过 PI3K/AKT 信号通路诱导脂质代谢紊乱并促进肥胖症的发生
磷酸三苯酯(TPHP)是一种应用广泛的有机磷酸盐阻燃剂,是一种潜在的环境致肥物质。然而,TPHP对脂肪组织的潜在影响和作用机制尚不清楚。本研究通过体内和体外实验探讨了TPHP对脂质代谢紊乱的潜在影响。雄性和雌性BALB/c小鼠分别暴露于TPHP(0、1、10和150 mg/kg/天)60 天,3个 T3-L1前脂肪细胞在分化过程中分别接受浓度为0、0.1、1、10 μM的TPHP处理。结果表明,暴露于TPHP可引起性别特异性血脂异常,雄性小鼠表现出剂量依赖性的腹股沟脂肪组织系数增加,脂肪细胞肥大,脂肪分化和脂肪形成相关基因上调。相比之下,雌性小鼠的组织形态没有明显变化。提示TPHP可能通过破坏男性脂肪组织脂质代谢稳态而促进肥胖的潜在发生。在3个 T3-L1前脂肪细胞的分化和成熟过程中,暴露于TPHP通过同时激活脂肪生成和脂肪分解导致脂质积累增加和脂质稳态破坏。多组学数据显示,激活过氧化物酶体增殖物激活受体γ (PPARγ)信号通路和脂肪酸代谢是TPHP诱导代谢功能障碍的核心机制。进一步研究表明,TPHP激活了PI3K/AKT通路,PI3K抑制剂LY294002可以挽救TPHP诱导的脂滴形成,使成脂标志物的表达正常化。这些发现证实,TPHP是一种潜在的环境致肥因子,可以通过PPARγ和PI3K/AKT信号通路破坏白色脂肪组织的代谢稳态,在男性中易感性更高。本研究为TPHP的致肥作用提供了有力证据,也为有机磷阻燃剂的风险评估提供了信息。
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来源期刊
Environment International
Environment International 环境科学-环境科学
CiteScore
21.90
自引率
3.40%
发文量
734
审稿时长
2.8 months
期刊介绍: Environmental Health publishes manuscripts focusing on critical aspects of environmental and occupational medicine, including studies in toxicology and epidemiology, to illuminate the human health implications of exposure to environmental hazards. The journal adopts an open-access model and practices open peer review. It caters to scientists and practitioners across all environmental science domains, directly or indirectly impacting human health and well-being. With a commitment to enhancing the prevention of environmentally-related health risks, Environmental Health serves as a public health journal for the community and scientists engaged in matters of public health significance concerning the environment.
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