Dourado Thales M H, Tirapelli Carlos R
Laboratório de Farmacologia Cardiovascular, Departamento de Ciências BioMoleculares, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo (USP), Ribeirão Preto, São Paulo, Brazil; Departamento de Farmacologia, Faculdade de Medicina de Ribeirão Preto, USP, Ribeirão Preto, São Paulo, Brazil.
Laboratório de Farmacologia Cardiovascular, Departamento de Ciências BioMoleculares, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo (USP), Ribeirão Preto, São Paulo, Brazil.
Am J Pathol. 2025 Aug 26. doi: 10.1016/j.ajpath.2025.07.012.
Adipose tissue plays a crucial role in energy storage, but it also acts as an endocrine organ by secreting hormones and proinflammatory molecules. It regulates various processes, including adipogenesis, metabolism, and inflammation. White and brown adipose tissue (WAT and BAT) consists of white and brown adipocytes, respectively, which differ in cellular structure and function. Adipocytes also make up a significant part of perivascular adipose tissue (PVAT), which forms a sheath-like structure around blood vessels. Current research indicates that WAT, BAT, and PVAT are negatively affected by ethanol (ethyl alcohol). The changes induced by ethanol in the storage, metabolic, and secretory functions of PVAT and WAT are linked to vascular and hepatic dysfunction. In this context, while adipose tissue is a target of the harmful effects of ethanol, it also contributes to its pathophysiological consequences. Although the function of BAT is impacted by ethanol, BAT exhibits a protective role against ethanol-induced liver disease. This review highlights both past and recent efforts to identify the mechanisms through which ethanol consumption alters adipocyte function, with a focus on findings from studies that explain the detrimental effects of ethanol on WAT and BAT, and discusses the interplay between adipose tissue and the liver, particularly its implications for alcoholic liver disease. Additionally, new data that elucidate the mechanisms underlying ethanol-induced dysfunction in PVAT are summarized.
脂肪组织在能量储存中起着关键作用,但它也通过分泌激素和促炎分子发挥内分泌器官的作用。它调节各种过程,包括脂肪生成、代谢和炎症。白色和棕色脂肪组织(WAT和BAT)分别由白色和棕色脂肪细胞组成,它们在细胞结构和功能上有所不同。脂肪细胞也是血管周围脂肪组织(PVAT)的重要组成部分,PVAT在血管周围形成鞘状结构。目前的研究表明,WAT、BAT和PVAT均受到乙醇(酒精)的负面影响。乙醇在PVAT和WAT的储存、代谢及分泌功能方面所引发的变化与血管和肝功能障碍有关。在此背景下,脂肪组织既是乙醇有害作用的靶点,又对其病理生理后果有一定影响。虽然BAT的功能受到乙醇影响,但BAT对乙醇诱导的肝病具有保护作用。本综述重点介绍了过去和近期为确定乙醇摄入改变脂肪细胞功能的机制所做的努力,着重阐述了解释乙醇对WAT和BAT有害影响的研究结果,并讨论了脂肪组织与肝脏之间的相互作用,特别是其对酒精性肝病的影响。此外,还总结了阐明乙醇诱导PVAT功能障碍潜在机制的新数据。