Department of Prophylaxis of Metabolic Diseases, Institute of Animal Reproduction and Food Research, Polish Academy of Sciences, Olsztyn, Poland.
Department of Metabolic Diseases, Medical University of Bialystok, Bialystok, Poland.
Nutr Metab Cardiovasc Dis. 2024 Nov;34(11):2455-2463. doi: 10.1016/j.numecd.2024.06.011. Epub 2024 Jun 20.
Adipose tissue (AT) serves as a vital energy storage site and plays a pivotal role in metabolic regulation, exhibiting a high response to insulin. Impairment in this response may closely associate with obesity, and NFAT (nuclear factor of activated T cells) family genes may be involved in the process. However, human data linking NFAT and AT remains elusive. The aim of this study was to assess the expression of NFAT family genes and markers of adipogenesis in subcutaneous adipose tissue (SAT) among normal-weight and overweight/obese individuals before and after weight loss, in relation to insulin sensitivity.
The study included 45 participants, 15 normal-weight (control group) and 30 overweight or obese, who underwent a 12-week dietary intervention (DI) program. Before and after the program hyperinsulinemic-euglycemic clamp and SAT biopsy were conducted. Before DI, a positive correlations was observed in the expression of NFATc1, NFATc4, and NFAT5 with insulin sensitivity. The expression of NFAT family genes and markers of adipogenesis in SAT was lower in individuals with overweight or obesity compared to normal-weight. Additionally, a positive correlation was noted between NFAT family genes and adipogenesis markers both before and after weight loss. Following the DI program, there was an increase in the expression of NFATc3, NFATc4, and NFAT5 in SAT.
Decreased SAT expression of NFAT genes in obesity is partly reversed in response to weight loss. NFAT genes in SAT are associated with insulin sensitivity and adipogenesis. Registration number for clinical trial: NCT01393210.
脂肪组织(AT)是重要的能量储存场所,在代谢调节中起着关键作用,对胰岛素有高度反应。这种反应的损害可能与肥胖密切相关,NFAT(激活 T 细胞的核因子)家族基因可能参与其中。然而,将 NFAT 与 AT 联系起来的人类数据仍然难以捉摸。本研究旨在评估 NFAT 家族基因在正常体重和超重/肥胖个体的皮下脂肪组织(SAT)中的表达,以及在减肥前后与胰岛素敏感性的关系。
本研究纳入了 45 名参与者,15 名正常体重(对照组)和 30 名超重或肥胖,他们接受了为期 12 周的饮食干预(DI)计划。在计划前后进行了高胰岛素-正葡萄糖钳夹和 SAT 活检。在 DI 之前,NFATc1、NFATc4 和 NFAT5 的表达与胰岛素敏感性呈正相关。与正常体重者相比,超重或肥胖者的 SAT 中 NFAT 家族基因和脂肪生成标志物的表达较低。此外,在减肥前后,NFAT 家族基因和脂肪生成标志物之间存在正相关。在 DI 计划后,SAT 中 NFATc3、NFATc4 和 NFAT5 的表达增加。
肥胖时 SAT 中 NFAT 基因的表达减少,部分在减肥后得到逆转。SAT 中的 NFAT 基因与胰岛素敏感性和脂肪生成有关。临床试验注册号:NCT01393210。