Ezzati-Mobaser Samira, Yarahmadi Sahar, Dadkhah Nikroo Nikta, Maleki Mohammad Hasan, Yousefi Zeynab, Golpour Pegah, Nourbakhsh Mona, Nourbakhsh Mitra
Finetech in Medicine Research Center Iran University of Medical Sciences Tehran Iran.
Department of Biochemistry Faculty of Medicine Iran University of Medical Sciences Tehran Iran.
Obes Sci Pract. 2023 Oct 25;10(1):e716. doi: 10.1002/osp4.716. eCollection 2024 Feb.
Adipose triglyceride lipase (ATGL) is a crucial enzyme responsible for the release of fatty acids from various tissues. The expression of ATGL is regulated by insulin and this enzyme is linked to Insulin resistance (IR). On the other hand, ATGL-mediated lipolysis is connected to macrophage function and thus, ATGL is involved in inflammation and the pathogenesis of lipid-related disorders. This study aimed to investigate the correlation between ATGL, obesity, Metabolic Syndrome (MetS), and inflammation.
A total of 100 participants, including 50 individuals with obesity and 50 healthy participants, were recruited for this study and underwent comprehensive clinical evaluations. Blood samples were collected to measure plasma lipid profiles, glycemic indices, and liver function tests. Additionally, peripheral blood mononuclear cells (PBMCs) were isolated and used for the assessment of the gene expression of ATGL, using real-time PCR. Furthermore, PBMCs were cultured and exposed to lipopolysaccharides (LPS) with simultaneous ATGL inhibition, and the gene expression of inflammatory cytokines, along with the secretion of prostaglandin E2 (PGE2), were measured.
The gene expression of ATGL was significantly elevated in PBMCs obtained from participants with obesity and was particularly higher in those diagnosed with MetS. It exhibited a correlation with insulin levels and Homeostatic Model Assessment for IR (HOMA-IR), and it was associated with lipid accumulation in the liver. Stimulation with LPS increased ATGL expression in PBMCs, while inhibition of ATGL attenuated the inflammatory responses induced by LPS.
Obesity and MetS were associated with dysregulation of ATGL. ATGL might play a role in the upregulation of inflammatory cytokines and act as a significant contributor to the development of metabolic abnormalities related to obesity.
脂肪甘油三酯脂肪酶(ATGL)是一种关键酶,负责从各种组织中释放脂肪酸。ATGL的表达受胰岛素调节,并且这种酶与胰岛素抵抗(IR)有关。另一方面,ATGL介导的脂肪分解与巨噬细胞功能相关,因此,ATGL参与炎症和脂质相关疾病的发病机制。本研究旨在探讨ATGL、肥胖、代谢综合征(MetS)和炎症之间的相关性。
本研究共招募了100名参与者,包括50名肥胖个体和50名健康参与者,并对他们进行了全面的临床评估。采集血样以测量血脂谱、血糖指标和肝功能测试。此外,分离外周血单核细胞(PBMC),并使用实时PCR评估ATGL的基因表达。此外,培养PBMC并使其暴露于脂多糖(LPS)并同时抑制ATGL,测量炎症细胞因子的基因表达以及前列腺素E2(PGE2)的分泌。
肥胖参与者的PBMC中ATGL的基因表达显著升高,在诊断为MetS的参与者中尤其更高。它与胰岛素水平和胰岛素抵抗稳态模型评估(HOMA-IR)呈相关性,并且与肝脏中的脂质积累有关。用LPS刺激可增加PBMC中ATGL的表达,而抑制ATGL可减弱LPS诱导的炎症反应。
肥胖和MetS与ATGL的失调有关。ATGL可能在炎症细胞因子的上调中起作用,并成为与肥胖相关的代谢异常发展的重要因素。