Naeini Zeinab, Toupchian Omid, Vatannejad Akram, Sotoudeh Gity, Teimouri Maryam, Ghorbani Mostafa, Nasli-Esfahani Ensieh, Koohdani Fariba
Department of Cellular and Molecular Nutrition, School of Nutritional Sciences and Dietetics, Tehran University of Medical Sciences, Tehran, Iran; Endocrinology and Metabolism Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.
Department of Nutrition and Public Health, School of Health, North Khorasan University of Medical Science, Bojnurd, Iran.
Nutr Metab Cardiovasc Dis. 2020 Mar 9;30(3):441-447. doi: 10.1016/j.numecd.2019.10.012. Epub 2019 Nov 5.
Omega-3 polyunsaturated fatty acids (PUFAs) are natural peroxisome proliferator-activated receptor gamma (PPAR-γ) ligands. Activated PPAR-γ protects the cardiovascular system against atherosclerotic lesion formation and exerts its anti-inflammatory role by suppressing cytokines induced by nuclear factor kappa-B (NF-κB) in endothelial cells (ECs), and it is hypothesized that apoptosis and cell cycle arrest induced by PPAR-γ ligands may be mediated by the p53-dependent pathway. The aim of our study was to investigate the effects of docosahexaenoic acid (DHA)-enriched fish oil supplement on PPAR-γ activity and mRNA expression levels of p53 and NF-κB.
Fifty patients with type 2 diabetes mellitus (T2DM) aged 30-70 years were randomly assigned to receive either 2400 mg/d DHA-rich fish oil or placebo for 8 weeks. Metabolic parameters were assessed at baseline and at the end of the intervention. PPAR-γ activity in the peripheral blood mononuclear cells (PBMCs) was measured using ELISA-based PPAR-γ Transcription Factor Assay Kit, and the gene expression levels of p53 and NF-κB were assessed using real-time quantitative reverse transcription polymerase chain reaction (RT-PCR). On the basis of our finding, 8 weeks of treatment with DHA-rich fish oil increased PPAR-γ activity in PBMCs of subjects with T2DM (p < 0.01) compared to that in placebo (p = 0.4). Between-group comparisons of mean PPAR-γ activity changes showed significant differences (p = 0.03), whereas mRNA expression levels of the p53 and NF-κB genes did not show significant differences between studied groups (p = 0.2 and p = 0.5, respectively).
Our findings indicated that short-term DHA-rich fish oil supplementation may modulate PPAR-γ activity in PBMCs.
ω-3多不饱和脂肪酸(PUFAs)是天然的过氧化物酶体增殖物激活受体γ(PPAR-γ)配体。激活的PPAR-γ可保护心血管系统免受动脉粥样硬化病变形成,并通过抑制内皮细胞(ECs)中核因子κB(NF-κB)诱导的细胞因子发挥其抗炎作用,并且据推测PPAR-γ配体诱导的细胞凋亡和细胞周期停滞可能由p53依赖性途径介导。我们研究的目的是探讨富含二十二碳六烯酸(DHA)的鱼油补充剂对PPAR-γ活性以及p53和NF-κB的mRNA表达水平的影响。
50例年龄在30 - 70岁的2型糖尿病(T2DM)患者被随机分配接受每日2400毫克富含DHA的鱼油或安慰剂,为期8周。在基线和干预结束时评估代谢参数。使用基于酶联免疫吸附测定(ELISA)的PPAR-γ转录因子检测试剂盒测量外周血单核细胞(PBMCs)中的PPAR-γ活性,并使用实时定量逆转录聚合酶链反应(RT-PCR)评估p53和NF-κB的基因表达水平。根据我们的研究结果,与安慰剂组(p = 0.4)相比,富含DHA的鱼油治疗8周可增加T2DM患者PBMCs中的PPAR-γ活性(p < 0.01)。PPAR-γ活性变化的组间均值比较显示出显著差异(p = 0.03),而p53和NF-κB基因的mRNA表达水平在研究组之间未显示出显著差异(分别为p = 0.2和p = 0.5)。
我们的研究结果表明,短期补充富含DHA的鱼油可能调节PBMCs中的PPAR-γ活性。