Faculty of Pharmacy, Research Institute for Medicines (iMed.ULisboa), Universidade de Lisboa, 1649-003, Lisbon, Portugal.
Department of Biochemistry and Human Biology, Faculty of Pharmacy, Universidade de Lisboa, 1649-003, Lisbon, Portugal.
Cell Mol Life Sci. 2018 Jun;75(11):1973-1988. doi: 10.1007/s00018-018-2781-4. Epub 2018 Feb 20.
The metabolic syndrome (MetS) includes a group of medical conditions such as insulin resistance (IR), dyslipidemia and hypertension, all associated with an increased risk for cardiovascular disease. Increased visceral and ectopic fat deposition are also key features in the development of IR and MetS, with pathophysiological sequels on adipose tissue, liver and muscle. The recent recognition of aquaporins (AQPs) involvement in adipose tissue homeostasis has opened new perspectives for research in this field. The members of the aquaglyceroporin subfamily are specific glycerol channels implicated in energy metabolism by facilitating glycerol outflow from adipose tissue and its systemic distribution and uptake by liver and muscle, unveiling these membrane channels as key players in lipid balance and energy homeostasis. Being involved in a variety of pathophysiological mechanisms including IR and obesity, AQPs are considered promising drug targets that may prompt novel therapeutic approaches for metabolic disorders such as MetS. This review addresses the interplay between adipose tissue, liver and muscle, which is the basis of the metabolic syndrome, and highlights the involvement of aquaglyceroporins in obesity and related pathologies and how their regulation in different organs contributes to the features of the metabolic syndrome.
代谢综合征(MetS)包括一组医学病症,如胰岛素抵抗(IR)、血脂异常和高血压,所有这些都与心血管疾病风险增加有关。内脏和异位脂肪沉积的增加也是 IR 和 MetS 发展的关键特征,对脂肪组织、肝脏和肌肉有病理生理后果。最近发现水通道蛋白(AQPs)参与脂肪组织稳态,为该领域的研究开辟了新的视角。水通道蛋白家族的成员是特定的甘油通道,通过促进脂肪组织中甘油的流出及其在肝脏和肌肉中的全身分布和摄取,参与能量代谢,揭示这些膜通道是脂质平衡和能量稳态的关键因素。AQPs 参与多种病理生理机制,包括 IR 和肥胖,被认为是有前途的药物靶点,可能为 MetS 等代谢紊乱提供新的治疗方法。这篇综述探讨了脂肪组织、肝脏和肌肉之间的相互作用,这是代谢综合征的基础,并强调了水通道蛋白在肥胖和相关病理中的作用,以及它们在不同器官中的调节如何有助于代谢综合征的特征。