Goffin Kay, van Maris Marc, Corbee Ronald J
Department of Clinical Sciences of Companion Animals, Faculty of Veterinary Medicine, Utrecht University, Yalelaan 108, 3584 CM Utrecht, The Netherlands.
Ayanda Concordix AS, Brynsveien 11-13, N-0667 Oslo, Norway.
J Nutr Sci. 2017 Jul 24;6:e37. doi: 10.1017/jns.2017.30. eCollection 2017.
EPA and DHA are often used in veterinary medicine due to their beneficial effects for several medical conditions such as osteoarthritis. EPA and DHA are administered to dogs through different matrices. The aim of the present study was to determine the effects on the plasma levels in dogs caused by various matrices for EPA and DHA administration. In this study, three different -3 PUFA formulations were used: soft chew tablet (CCx); liquid fish oil (LFO); and enriched kibbles (EK). The formulations were administered single-dose and compared in a randomised, cross-over designed study with a 1-week wash-out period. Several variables were observed after the administration of these formulations in thirteen dogs: the NEFA plasma concentration, the AUC for 1 d (AUC0-24 h), and maximum plasma concentration for both EPA and DHA. All plasma fatty acid levels reached baseline levels within 72 h. CCx (median = 2·987) had a significantly lower AUC0-24 h for EPA compared with LFO (median = 5·647, = 0·043) and EK (median = 5·119, = 0·032) ( = 4·637, = 0·021). CCx (median = 2·471) AUC0-24 h for DHA was significantly lower compared with LFO (median = 4·837, = -2·56, = 0·011) and EK (median = 4·413, = -2·59, = 0·01). EPA and DHA plasma levels were affected by matrix, as with the CCx, the AUC0-24 h of EPA and DHA were both lower compared with LFO and EK. The effect of matrix on bioavailability is important for product development as well as for clinical trials studying effects of EPA and DHA.
由于二十碳五烯酸(EPA)和二十二碳六烯酸(DHA)对骨关节炎等多种病症具有有益作用,它们常用于兽医学。EPA和DHA通过不同基质给予犬类。本研究的目的是确定不同EPA和DHA给药基质对犬血浆水平的影响。在本研究中,使用了三种不同的ω-3多不饱和脂肪酸制剂:软咀嚼片(CCx);液体鱼油(LFO);以及强化狗粮(EK)。这些制剂采用单剂量给药,并在一项为期1周洗脱期的随机交叉设计研究中进行比较。在13只犬给予这些制剂后观察了几个变量:非酯化脂肪酸血浆浓度、1天的曲线下面积(AUC0-24 h)以及EPA和DHA的最大血浆浓度。所有血浆脂肪酸水平在72小时内恢复到基线水平。与LFO(中位数=5.647,P=0.043)和EK(中位数=5.119,P=0.032)相比,CCx(中位数=2.987)的EPA的AUC0-24 h显著更低(P=4.637,P=0.021)。与LFO(中位数=4.837,P=-2.56,P=0.011)和EK(中位数=4.413,P=-2.59,P=0.01)相比,CCx(中位数=2.471)的DHA的AUC0-24 h显著更低。EPA和DHA的血浆水平受基质影响,与CCx一样,EPA和DHA的AUC0-24 h均低于LFO和EK。基质对生物利用度的影响对于产品开发以及研究EPA和DHA作用的临床试验都很重要。