AbuGhazaleh A A, Jenkins T C
Department of Animal and Veterinary Sciences, Clemson University, Clemson, SC 29634, USA.
J Dairy Sci. 2004 Mar;87(3):645-51. doi: 10.3168/jds.S0022-0302(04)73207-5.
Previous studies showed conflicting results regarding the ability of ruminal microorganisms to hydrogenate docosahexaenoic acid (C22:6, DHA) and eicosapentaenoic acid (C20:5, EPA). To determine the disappearance of DHA and EPA from mixed ruminal cultures, 2 ruminal in vitro experiments were conducted using graded levels of DHA and EPA. The first experiment examined DHA added at 0, 5, 10, 15, and 20 mg per culture flask. In the second experiment, EPA was added at 0, 5, 10, and 15 mg per culture flask. Docosahexaenoic acid and EPA were incubated in triplicate in 125-mL flasks, and 5 mL of culture contents was taken at 0, 12, and 24 h for fatty acid analysis by gas liquid chromatography. After 24 h of incubation, 4.1, 4.1, 4.0, and 3.3 mg of DHA disappeared from the 5, 10, 15, and 20 mg of DHA cultures, respectively. In the second experiment, 5, 8.3, and 7.1 mg of EPA disappeared after 24 h of incubation for the 5-, 10-, and 15-mg EPA cultures, respectively. Addition of DHA to cultures increased trans-C18:1 fatty acid accumulation by 105, 91, 82, and 74% for the 5, 10-, 15-, and 20-mg cultures, respectively, compared with control. The addition of EPA increased trans-C18:1 fatty acid accumulation by 56, 64, and 55% for the 5-, 10-, and 15-mg EPA cultures, respectively, compared with control. Addition of DHA and EPA to cultures caused a reduction in C18:1 n-9 and C18:2 n-6 biohydrogenation compared with control. Results from these experiments clearly demonstrate the ability of ruminal microorganism to transform DHA and EPA to other fatty acids causing their disappearance from cultures.
先前的研究表明,关于瘤胃微生物氢化二十二碳六烯酸(C22:6,DHA)和二十碳五烯酸(C20:5,EPA)的能力,结果相互矛盾。为了确定混合瘤胃培养物中DHA和EPA的消失情况,进行了2项瘤胃体外实验,使用了不同水平的DHA和EPA。第一个实验检测了每个培养瓶中添加0、5、10、15和20毫克DHA的情况。在第二个实验中,每个培养瓶中添加0、5、10和15毫克EPA。二十二碳六烯酸和EPA在125毫升的培养瓶中一式三份进行孵育,在0、12和24小时分别取5毫升培养物内容物,通过气相色谱法进行脂肪酸分析。孵育24小时后,5、10、15和20毫克DHA培养物中分别有4.1、4.1、4.0和3.3毫克DHA消失。在第二个实验中,5、10和15毫克EPA培养物在孵育24小时后,分别有5、8.3和7.1毫克EPA消失。与对照相比,向培养物中添加DHA使5、10、15和20毫克培养物中的反式C18:1脂肪酸积累分别增加了105%、91%、82%和74%。与对照相比,添加EPA使5、10和15毫克EPA培养物中的反式C18:1脂肪酸积累分别增加了56%、64%和55%。与对照相比,向培养物中添加DHA和EPA导致C18:1 n-9和C18:2 n-6生物氢化减少。这些实验结果清楚地证明了瘤胃微生物将DHA和EPA转化为其他脂肪酸并使其从培养物中消失的能力。