长链n-3 PUFA对肥胖人群肝脏转录组的影响。

IF 3
Rebeka Joerg , Bianca K. Itariu , Melina Amor , Martin Bilban , Felix Langer , Gerhard Prager , Florian Joerg , Thomas M. Stulnig
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引用次数: 0

摘要

背景和目的:肥胖与严重疾病的高风险相关,如动脉粥样硬化性心血管疾病、2型糖尿病(T2DM)和代谢功能障碍相关的脂肪变性肝病(MASLD)。omega-3家族的多不饱和脂肪酸(n-3 PUFA)已被证明可以减少肥胖的脂肪组织炎症,以及具有降脂作用和改善胰岛素敏感性。然而,对人类肝脏转录组的直接影响尚未被描述。我们的目的是了解n-3 PUFA对肥胖人类肝脏基因表达的影响。方法和结果:肥胖患者(BMI≥40 kg/m2)接受3.36 g n-3 PUFAs (1.84 g二十碳五烯酸(EPA)和1.53 g二十二碳六烯酸(DHA))或5 g黄油作为对照(每组n = 15)治疗8周,然后进行减肥手术,并进行肝活检。肝脏样本用于mRNA微阵列分析,随后进行基因集富集分析(GSEA)。这种生物信息学方法使我们确定了80个显着失调的途径,这些途径分为9个不同的簇,包括胰岛素和脂质代谢以及免疫。N-3 PUFA治疗显著影响与免疫、代谢和炎症相关的途径。具体来说,它上调了t细胞和b细胞功能和脂质代谢的通路,同时下调了胰高血糖素信号传导。这些发现强调了n-3 PUFAs对肥胖患者肝脏关键代谢和免疫过程的影响。结论:本研究进一步揭示了n-3 PUFA对人肝脏基因表达的影响,特别是对免疫、脂质代谢和炎症相关通路的影响,为进一步的临床研究奠定了基础。总结:肥胖增加了动脉粥样硬化性心血管疾病、2型糖尿病和代谢功能障碍相关脂肪变性肝病(MASLD)等疾病的风险。Omega-3多不饱和脂肪酸(n-3 PUFA)因其抗炎和代谢益处而闻名,但其对肥胖人群肝脏基因表达的直接影响尚不清楚。在这项研究中,肥胖患者(BMI≥40 kg/m2)在减肥手术前给予n-3 PUFAs或黄油。通过基因集富集分析(GSEA)对肝活检组织进行基因表达分析。结果显示,在9个簇中有80条通路失调,包括与胰岛素和脂质代谢以及免疫相关的通路。这揭示了n-3 PUFAs如何影响肥胖患者肝脏中的基因表达,为进一步的临床探索奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effect of long-chain n-3 PUFA on liver transcriptome in human obesity

Background and aims

Obesity is associated with a higher risk of severe diseases such as atherosclerotic cardiovascular disease, type 2 diabetes mellitus (T2DM), and metabolic dysfunction-associated steatotic liver disease (MASLD). Polyunsaturated fatty acids, of the omega-3 family (n-3 PUFA), have been shown to reduce adipose tissue inflammation in obesity, as well as to have lipid-lowering effects and improve insulin sensitivity. However, direct effects on liver transcriptome in humans have not been described. Our aim was to understand the impact of n-3 PUFA on gene expression in obese human liver.

Approach and Results

Patients with obesity (BMI 40 kg/m2) were treated for eight weeks with 3.36 g n-3 PUFAs (1.84 g eicosapentaenoic acid (EPA) and 1.53 g docosahexaenoic acid (DHA)), or with 5 g of butter as a control (n = 15 per group) before undergoing bariatric surgery where liver biopsies were taken. Liver samples were used for mRNA microarray analyses and subsequently Gene Set Enrichment Analysis (GSEA) was performed. This bioinformatic approach led us to identify 80 significantly dysregulated pathways that were divided into 9 different clusters including insulin and lipid metabolism, and immunity. N-3 PUFA treatment significantly affected pathways related to immunity, metabolism, and inflammation. Specifically, it upregulated pathways involved in T-cell and B-cell functions and lipid metabolism, while downregulating glucagon signalling. These findings highlight the impact of n-3 PUFAs on key metabolic and immune processes in the liver of patients with obesity.

Conclusion

This study provides further insights into the impact on n-3 PUFA on human liver gene expression, particularly in pathways associated with immunity, lipid metabolism, and inflammation, setting basis for further clinical research.

Summary

Obesity increases the risk of diseases like atherosclerotic- cardiovascular disease, type 2 diabetes mellitus and metabolic dysfunction-associated steatotic liver disease (MASLD). Omega-3 polyunsaturated fatty acids (n-3 PUFA) are known for their anti-inflammatory and metabolic benefits, but their direct impact on liver gene expression in people with obesity, remains unclear. In this study, patients with obesity (BMI ≥ 40 kg/m2) were administered either n-3 PUFAs or butter before bariatric surgery. Liver biopsies were analysed for gene expression via Gene Set Enrichment Analysis (GSEA). The results revealed 80 dysregulated pathways across 9 clusters, including those related to insulin and lipid metabolism, and immunity. This sheds light on how n-3 PUFAs influence gene expression in the liver of patients with obesity, setting the groundwork for further clinical exploration.
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来源期刊
Prostaglandins, leukotrienes, and essential fatty acids
Prostaglandins, leukotrienes, and essential fatty acids Clinical Biochemistry, Endocrinology, Diabetes and Metabolism
CiteScore
5.30
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64 days
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