de Lima Enzo Pereira, Moretti Renato Cesar, Torres Pomini Karina, Laurindo Lucas Fornari, Sloan Kátia Portero, Sloan Lance Alan, Castro Marcela Vialogo Marques de, Baldi Edgar, Ferraz Bruna Fidencio Rahal, de Souza Bastos Mazuqueli Pereira Eliana, Catharin Virgínia Maria Cavallari Strozze, Mellen Carolina Haber, Caracio Flávia Cristina Castilho, Spilla Caio Sérgio Galina, Haber Jesselina F S, Barbalho Sandra Maria
Department of Biochemistry and Pharmacology, School of Medicine, Universidade de Marília (UNIMAR), Marília 17525-902, SP, Brazil.
Postgraduate Program in Structural and Functional Interactions in Rehabilitation, School of Medicine, Universidade de Marília (UNIMAR), Marília 17525-902, SP, Brazil.
Biology (Basel). 2024 Jul 12;13(7):519. doi: 10.3390/biology13070519.
Glycolipid metabolic disorders (GLMDs) are various metabolic disorders resulting from dysregulation in glycolipid levels, consequently leading to an increased risk of obesity, diabetes, liver dysfunction, neuromuscular complications, and cardiorenal vascular diseases (CRVDs). In patients with GLMDs, excess caloric intake and a lack of physical activity may contribute to oxidative stress (OxS) and systemic inflammation. This study aimed to review the connection between GLMD, OxS, metainflammation, and the onset of CRVD. GLMD is due to various metabolic disorders causing dysfunction in the synthesis, breakdown, and absorption of glucose and lipids in the body, resulting in excessive ectopic accumulation of these molecules. This is mainly due to neuroendocrine dysregulation, insulin resistance, OxS, and metainflammation. In GLMD, many inflammatory markers and defense cells play a vital role in related tissues and organs, such as blood vessels, pancreatic islets, the liver, muscle, the kidneys, and adipocytes, promoting inflammatory lesions that affect various interconnected organs through their signaling pathways. Advanced glycation end products, ATP-binding cassette transporter 1, Glucagon-like peptide-1, Toll-like receptor-4, and sphingosine-1-phosphate (S1P) play a crucial role in GLMD since they are related to glucolipid metabolism. The consequences of this is system organ damage and increased morbidity and mortality.
糖脂代谢紊乱(GLMDs)是由糖脂水平失调引起的各种代谢紊乱,进而导致肥胖、糖尿病、肝功能障碍、神经肌肉并发症和心肾血管疾病(CRVDs)风险增加。在GLMD患者中,热量摄入过多和缺乏体育活动可能会导致氧化应激(OxS)和全身炎症。本研究旨在综述GLMD、OxS、代谢性炎症与CRVD发病之间的联系。GLMD是由于各种代谢紊乱导致体内葡萄糖和脂质的合成、分解及吸收功能障碍,从而使这些分子在异位过度蓄积。这主要是由于神经内分泌失调、胰岛素抵抗、OxS和代谢性炎症所致。在GLMD中,许多炎症标志物和防御细胞在相关组织和器官(如血管、胰岛、肝脏、肌肉、肾脏和脂肪细胞)中发挥着至关重要的作用,通过其信号通路促进炎症性病变,影响各种相互关联的器官。晚期糖基化终产物、ATP结合盒转运体1、胰高血糖素样肽-1、Toll样受体4和鞘氨醇-1-磷酸(S1P)在GLMD中起着关键作用,因为它们与糖脂代谢有关。其后果是系统器官损伤以及发病率和死亡率增加。