Mohammadi Farzad, Beauparlant Charles Joly, Bianco Stéphanie, Droit Arnaud, Bertrand Nicolas, Rudkowska Iwona
Endocrinology and Nephrology Unit, CHU de Québec-Université Laval Research Center, Québec, Canada.
Département de Kinésiologie, Université Laval, Québec, Canada.
Mol Nutr Food Res. 2024 Nov;68(21):e2400290. doi: 10.1002/mnfr.202400290. Epub 2024 Oct 13.
The study aims to analyze transcriptomic profiles in adipose tissues postconsumption of elaidic acid (EA; trans-18:1n-9) and trans-palmitoleic acid (TPA; trans-16:1n-7), elucidating their different effects on inflammation and glucose metabolism.
Twenty C57BL/6 mice are divided into four groups. Each group receives one of the following formulations in drinking water: lecithin nanovesicles, nanovesicles containing either lecithin with EA or TPA (86:14 w/w), or water (control) for 28 days with a regular fat diet (18% calories from fat). Total RNA is extracted, and paired-end sequencing is performed. TPA intake alters the expression of 351 genes compared to EA intake, including 11 downregulated and 340 upregulated genes (fold change [FC] >1.5, p < 0.05). TPA compares to EA upregulated: Slc5a8, Lcn2, Csf3, Scube1, Mapk13, Bdkrb2, Ctla2a, Slc2a1, Oas3, Cx3cl1, Oas2, Nlrp6, Pycard, Cyba, Ddr1, and Prkab1 and downregulated Fas gene. These genes are related to the NOD-like receptor, lipid and atherosclerosis, IL-17 signaling, TNF, nonalcoholic fatty liver disease, cytokine-cytokine receptor interaction, adipocytokine, glucagon, insulin resistance, and inflammatory mediator regulation of TRP channels signaling.
TPA intake has a distinct impact on the regulation of inflammation and diabetes-related pathways in adipose tissue compared to EA.
本研究旨在分析食用反式油酸(EA;反式-18:1n-9)和反式棕榈油酸(TPA;反式-16:1n-7)后脂肪组织中的转录组图谱,阐明它们对炎症和葡萄糖代谢的不同影响。
将20只C57BL/6小鼠分为四组。每组在饮用水中接受以下制剂之一:卵磷脂纳米囊泡、含有卵磷脂与EA或TPA(86:14 w/w)的纳米囊泡,或水(对照),持续28天,并给予常规脂肪饮食(脂肪提供18%的热量)。提取总RNA,并进行双端测序。与摄入EA相比,摄入TPA改变了351个基因的表达,包括11个下调基因和340个上调基因(倍数变化[FC]>1.5,p<0.05)。与EA相比,TPA上调的基因有:Slc5a8、Lcn2、Csf3、Scube1、Mapk13、Bdkrb2、Ctla2a、Slc2a1、Oas3、Cx3cl1、Oas2、Nlrp6、Pycard、Cyba、Ddr1和Prkab1,下调的基因是Fas。这些基因与NOD样受体、脂质和动脉粥样硬化、IL-17信号传导、TNF、非酒精性脂肪性肝病、细胞因子-细胞因子受体相互作用、脂肪细胞因子、胰高血糖素、胰岛素抵抗以及TRP通道信号传导的炎症介质调节有关。
与EA相比,摄入TPA对脂肪组织中炎症和糖尿病相关途径的调节有明显影响。