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脂肪组织作为环境毒物的作用靶点:聚焦代谢功能障碍相关脂肪性肝病中的线粒体功能障碍和氧化炎症

Adipose tissue as target of environmental toxicants: focus on mitochondrial dysfunction and oxidative inflammation in metabolic dysfunction-associated steatotic liver disease.

作者信息

Lolescu Bogdan M, Furdui-Lința Adina V, Ilie Cosmin A, Sturza Adrian, Zară Flavia, Muntean Danina M, Blidișel Alexandru, Crețu Octavian M

机构信息

Doctoral School Medicine, Center for Translational Research and Systems Medicine, "Victor Babeș" University of Medicine and Pharmacy of Timișoara, Timișoara, Romania.

Center for Translational Research and Systems Medicine, "Victor Babeș" University of Medicine and Pharmacy of Timișoara, Timișoara, Romania.

出版信息

Mol Cell Biochem. 2025 May;480(5):2863-2879. doi: 10.1007/s11010-024-05165-z. Epub 2024 Dec 20.

Abstract

Obesity, diabetes, and their cardiovascular and hepatic comorbidities are alarming public health issues of the twenty-first century, which share mitochondrial dysfunction, oxidative stress, and chronic inflammation as common pathophysiological mechanisms. An increasing body of evidence links the combined exposure to multiple environmental toxicants with the occurrence and severity of metabolic diseases. Endocrine disruptors (EDs) are ubiquitous chemicals or mixtures with persistent deleterious effects on the living organisms beyond the endocrine system impairment; in particular, those known as metabolism-disrupting chemicals (MDCs), increase the risk of the metabolic pathologies in adult organism or its progeny. Being largely lipophilic, MDCs mainly target the adipose tissue and elicit mitochondrial dysfunction by interfering with mitochondrial bioenergetics, biogenesis, dynamics and/or other functions. Plastics, when broken down into micro- and nano-plastics (MNPs), have been detected in several human tissues, including the liver. The harmful interplay between inflammatory and redox processes, which mutually interact in a positive feed-back loop, hence the term oxidative inflammation ("OxInflammation"), occurs both at systemic and organ level. In both liver and adipose tissue, oxinflammation contributes to the progression of the metabolic dysfunction-associated steatotic liver disease (MASLD). Moreover, it has been reported that individuals with MASLD may be more susceptible to the harmful effects of toxicants (mainly, those related to mitochondria) and that chronic exposure to EDs/MDCs or MNPs may play a role in the development of the disease. While liver has been systematically investigated as major target organ for ambient chemicals, surprisingly, less information is available in the literature with respect to the adipose tissue. In this narrative review, we delve into the current literature on the most studied environmental toxicants (bisphenols, polychlorinated biphenyls, phthalates, tolylfluanid and tributyltin, per-fluoroalkyl and polyfluoroalkyl substances, heavy metals and MNPs), summarize their deleterious effects on adipose tissue, and address the role of dysregulated mitochondria and oxinflammation, particularly in the setting of MASLD.

摘要

肥胖、糖尿病及其心血管和肝脏合并症是21世纪令人担忧的公共卫生问题,它们都存在线粒体功能障碍、氧化应激和慢性炎症等共同的病理生理机制。越来越多的证据表明,多种环境毒物的联合暴露与代谢性疾病的发生和严重程度有关。内分泌干扰物(EDs)是普遍存在的化学物质或混合物,除了损害内分泌系统外,还对生物体具有持续的有害影响;特别是那些被称为代谢干扰化学物质(MDCs)的物质,会增加成年生物体或其后代患代谢性疾病的风险。由于MDCs具有很强的亲脂性,它们主要靶向脂肪组织,并通过干扰线粒体生物能量学、生物发生、动力学和/或其他功能引发线粒体功能障碍。塑料分解成微塑料和纳米塑料(MNPs)后,已在包括肝脏在内的多种人体组织中被检测到。炎症和氧化还原过程之间的有害相互作用在全身和器官水平上都存在,它们在正反馈回路中相互作用,因此被称为氧化炎症(“OxInflammation”)。在肝脏和脂肪组织中,氧化炎症都促进了与代谢功能障碍相关的脂肪性肝病(MASLD)的进展。此外,有报道称,患有MASLD的个体可能更容易受到毒物(主要是与线粒体相关的毒物)的有害影响,长期暴露于EDs/MDCs或MNPs可能在该疾病的发展中起作用。虽然肝脏已被系统地研究为环境化学物质的主要靶器官,但令人惊讶的是,关于脂肪组织的文献资料较少。在这篇叙述性综述中,我们深入研究了目前关于研究最多的环境毒物(双酚类、多氯联苯、邻苯二甲酸盐、甲苯氟磺胺和三丁基锡、全氟烷基和多氟烷基物质、重金属和MNPs)的文献,总结了它们对脂肪组织的有害影响,并探讨了线粒体失调和氧化炎症的作用,特别是在MASLD背景下的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55e0/12048461/05ebead5cc6f/11010_2024_5165_Fig1_HTML.jpg

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