Institute of Food Science and Human Nutrition, Leibniz University of Hannover, Am Kleinen Felde 30, 30167, Hannover, Germany.
Lipids Health Dis. 2012 Aug 29;11:105. doi: 10.1186/1476-511X-11-105.
Epidemiological studies have suggested the benefits of omega-3 polyunsaturated fatty acids (n-3 PUFAs) on cardiovascular health, but only limited data are available describing n-3 PUFA regulated pathways in humans. The aim of this study was to investigate the effects of n-3 PUFA administration on whole genome expression profiles in the blood of normo- and dyslipidemic subjects.
Differentially expressed genes were detected after four hours, one week and twelve weeks of supplementation with either fish oil (FO) or corn oil in normo- and dyslipidemic men using whole genome microarrays.
Independent of the oil, a significantly higher number of genes was regulated in dyslipidemic subjects compared to normolipidemic subjects. Pathway analyses discovered metabolisms dominantly affected by FO after twelve weeks of supplementation, including the lipid metabolism, immune system and cardiovascular diseases. Several pro-inflammatory genes, in particular, were down-regulated in dyslipidemic subjects, indicating the immune-modulatory and anti-inflammatory capability of FO and its bioactive FAs, eicosapentaenoic acid and docosahexaenoic acid.
This is the first study showing significant differences in gene expression profiles between normo- and dyslipidemic men after FO supplementation. Further studies need to clarify the exact role of n-3 PUFAs in pathways and metabolisms which were identified as being regulated after FO supplementation in this study.
ClinicalTrials.gov (ID: NCT01089231).
流行病学研究表明,ω-3 多不饱和脂肪酸(n-3PUFAs)对心血管健康有益,但目前仅有有限的数据描述了 n-3PUFA 在人体中的调节途径。本研究旨在探讨 n-3PUFA 给药对正常和血脂异常受试者血液全基因组表达谱的影响。
使用全基因组微阵列,在正常和血脂异常男性中分别用鱼油(FO)或玉米油进行为期四周、一周和十二周的补充后,检测差异表达基因。
独立于油,血脂异常受试者中受调控的基因数量明显高于正常血脂受试者。通路分析发现,十二周补充 FO 后,代谢物主要受 FO 调节,包括脂质代谢、免疫系统和心血管疾病。一些促炎基因,特别是在血脂异常受试者中下调,表明 FO 及其生物活性 FAs(二十碳五烯酸和二十二碳六烯酸)具有免疫调节和抗炎作用。
这是第一项研究,表明在 FO 补充后,正常和血脂异常男性的基因表达谱存在显著差异。进一步的研究需要阐明 n-3PUFAs 在本研究中确定的 FO 补充后被调节的途径和代谢物中的确切作用。
ClinicalTrials.gov(ID:NCT01089231)。