Ulven Stine M, Holven Kirsten B
Department of Health, Nutrition and Management, Faculty of Health Sciences, Oslo and Akershus University College of Applied Sciences, Oslo, Norway.
Department of Nutrition, Institute for Basic Medical Sciences, University of Oslo, Oslo, Norway.
Vasc Health Risk Manag. 2015 Aug 28;11:511-24. doi: 10.2147/VHRM.S85165. eCollection 2015.
The aim of this review is to summarize the effects of krill oil (KO) or fish oil (FO) on eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) incorporation in plasma phospholipids or membrane of red blood cells (RBCs) as shown in human and animal studies. Furthermore, we discuss the findings in relation to the possible different health effects, focusing on lipids, inflammatory markers, cardiovascular disease risk, and biological functions of these two sources of long-chain n-3 polyunsaturated fatty acids (PUFAs).
A literature search was conducted in PubMed in January 2015. In total, 113 articles were identified, but based on selection criteria, 14 original papers were included in the review.
Studies on bioavailability of EPA and DHA from KO and FO in humans and animals are limited and the interpretation is difficult, as different amounts of EPA and DHA have been used, duration of intervention differs, and different study groups have been included. Two human studies--one postprandial study and one intervention study--used the same amount of EPA and DHA from KO or FO, and they both showed that the bioavailability of EPA and DHA from KO seems to be higher than that from FO. Limited effects of KO and FO on lipids and inflammatory markers in human and animal studies were reported. Gene expression data from animal studies showed that FO upregulated the cholesterol synthesis pathway, which was the opposite of the effect mediated by KO. KO also regulated far more metabolic pathways than FO, which may indicate different biological effects of KO and FO.
There seems to be a difference in bioavailability of EPA and DHA after intake of KO and FO, but more studies are needed before a firm conclusion can be made. It is also necessary to document the beneficial health effects of KO with more human studies and to elucidate if these effects differ from those after regular fish and FO intake.
本综述旨在总结磷虾油(KO)或鱼油(FO)对人体和动物研究中所示的二十碳五烯酸(EPA)和二十二碳六烯酸(DHA)掺入血浆磷脂或红细胞(RBC)膜的影响。此外,我们讨论了与可能的不同健康影响相关的研究结果,重点关注这两种长链n-3多不饱和脂肪酸(PUFA)来源的脂质、炎症标志物、心血管疾病风险和生物学功能。
2015年1月在PubMed上进行了文献检索。总共识别出113篇文章,但根据选择标准,14篇原始论文被纳入综述。
关于人体和动物中KO和FO中EPA和DHA生物利用度的研究有限且难以解释,因为使用的EPA和DHA量不同,干预持续时间不同,并且纳入了不同的研究组。两项人体研究——一项餐后研究和一项干预研究——使用了相同量的来自KO或FO的EPA和DHA,并且它们都表明来自KO的EPA和DHA的生物利用度似乎高于来自FO的。在人体和动物研究中报道了KO和FO对脂质和炎症标志物的有限影响。动物研究的基因表达数据表明,FO上调了胆固醇合成途径,这与KO介导的作用相反。KO还比FO调节更多的代谢途径,这可能表明KO和FO具有不同的生物学效应。
摄入KO和FO后,EPA和DHA的生物利用度似乎存在差异,但在得出确凿结论之前还需要更多研究。还需要通过更多人体研究来证明KO对健康的有益影响,并阐明这些影响是否与常规食用鱼类和FO后的影响不同。