Lobato Sagrario, Salomón-Soto Víctor Manuel, Espinosa-Méndez Claudia Magaly, Herrera-Moreno María Nancy, García-Solano Beatriz, Pérez-González Ernestina, Comba-Marcó-Del-Pont Facundo, Montesano-Villamil Mireya, Mora-Ramírez Marco Antonio, Mancilla-Simbro Claudia, Álvarez-Valenzuela Ramiro
Departamento de Investigación en Salud, Servicios de Salud del Estado de Puebla, 603 North 6th Street, Centro Colony, Puebla 72000, Mexico.
Clínica de Medicina Familiar con Especialidades y Quirófano ISSSTE, 27 North Street 603, Santa Maria la Rivera Colony, Puebla 72045, Mexico.
Biomolecules. 2024 Dec 16;14(12):1607. doi: 10.3390/biom14121607.
Obesity, influenced by environmental pollutants, can lead to complex metabolic disruptions. This systematic review and meta-analysis examined the molecular mechanisms underlying metabolically abnormal obesity caused by exposure to a high-fat diet (HFD) and fine particulate matter (PM). Following the PRISMA guidelines, articles from 2019 to 2024 were gathered from Scopus, Web of Science, and PubMed, and a random-effects meta-analysis was performed, along with subgroup analyses and pathway enrichment analyses. This study was registered in the Open Science Framework. Thirty-three articles, mainly case-control studies and murine models, were reviewed, and they revealed that combined exposure to HFD and PM resulted in the greatest weight gain (82.835 g, = 0.048), alongside increases in high-density lipoproteins, insulin, and the superoxide dismutase. HFD enriched pathways linked to adipocytokine signaling in brown adipose tissue, while PM impacted genes associated with fat formation. Both exposures downregulated protein metabolism pathways in white adipose tissue and activated stress-response pathways in cardiac tissue. Peroxisome proliferator-activated receptor and AMP-activated protein kinase signaling pathways in the liver were enriched, influencing non-alcoholic fatty liver disease. These findings highlight that combined exposure to HFD and PM amplifies body weight gain, oxidative stress, and metabolic dysfunction, suggesting a synergistic interaction with significant implications for metabolic health.
受环境污染物影响的肥胖会导致复杂的代谢紊乱。本系统评价和荟萃分析研究了高脂饮食(HFD)和细颗粒物(PM)暴露所致代谢异常性肥胖的分子机制。按照PRISMA指南,从Scopus、Web of Science和PubMed收集了2019年至2024年的文章,并进行了随机效应荟萃分析以及亚组分析和通路富集分析。本研究已在开放科学框架中注册。共审查了33篇文章,主要是病例对照研究和小鼠模型,结果显示,同时暴露于HFD和PM导致体重增加最多(82.835 g, = 0.048),同时高密度脂蛋白、胰岛素和超氧化物歧化酶增加。HFD使棕色脂肪组织中与脂肪细胞因子信号传导相关的通路富集,而PM影响与脂肪形成相关的基因。两种暴露均下调白色脂肪组织中的蛋白质代谢通路,并激活心脏组织中的应激反应通路。肝脏中的过氧化物酶体增殖物激活受体和AMP激活的蛋白激酶信号通路富集,影响非酒精性脂肪性肝病。这些发现突出表明,同时暴露于HFD和PM会加剧体重增加、氧化应激和代谢功能障碍,提示存在协同相互作用,对代谢健康具有重大影响。