Kumamoto T, Ide T
Laboratory of Nutrition Biochemistry, National Food Research Institute, Ministry of Agriculture, Forestry and Fisheries, Tsukuba Science City, Japan.
Lipids. 1998 Jul;33(7):647-54. doi: 10.1007/s11745-998-0252-4.
It has been reported that both n-3 and n-6 octadecatrienoic acids can increase hepatic fatty acid oxidation activity. It remains unclear, however, whether different enzymes in fatty acid oxidation show a similar response to n-3 and n-6 octadecatrienoic acids. The activity of hepatic fatty acid oxidation enzymes in rats fed an oil mixture rich in alpha-linolenic acid (18:3n-3) and borage oil rich in gamma-linolenic acid (18:3n-6) was therefore compared to that in rats fed an oil mixture rich in linoleic acid (18:2n-6) and a saturated fat (palm oil) in this study. Linseed oil served as the source of 18:3n-3 for the oil mixture rich in this octadecatrienoic acid and contained 30.6% 18:3n-3 but not 18:3n-6. Borage oil contained 25.7% 18:3n-6 and 4.5% 18:3n-3. Groups of seven rats each were fed diets containing 15% various fats for 15 d. The oxidation rate of palmitoyl-CoA in the peroxisomes was higher in rats fed a fat mixture rich in 18:3n-3 (3.03 nmol/min/mg protein) and borage oil (2.89 nmol/min/mg protein) than in rats fed palm oil (2.08 nmol/min/mg protein) and a fat mixture rich in 18:2n-6 (2.15 nmol/min/mg protein). The mitochondrial palmitoyl-CoA oxidation rate was highest in rats fed a fat mixture rich in 18:3n-3 (1.93 nmol/min/mg protein), but no significant differences in this parameter were seen among the other groups (1.25-1.46 nmol/min/mg protein). Compared to palm oil and fat mixtures rich in 18:2n-6, a fat mixture rich in 18:3n-3 and borage oil significantly increased the hepatic activity of carnitine palmitoyltransferase and acyl-CoA oxidase. Compared to palm oil and a fat mixture rich in 18:2n-6, a fat mixture rich in 18:3n-3, but not fats rich in 18:3n-6, significantly decreased 3-hydroxyacyl-CoA dehydrogenase activity. Compared to palm oil and a fat mixture rich in 18:2n-6, borage oil profoundly decreased mitochondrial acyl-CoA dehydrogenase activity, but a fat mixture rich in 18:3n-3 increased it. 2,4-Dienoyl-CoA reductase activity was significantly lower in rats fed palm oil than in other groups. Compared to other fats, borage oil significantly increased delt3,delta2-enoyl-CoA isomerase activity. Activity was also significantly higher in rats fed 18:2n-6 oil than in those fed palm oil. It was confirmed that both dietary 18:3n-6 and 18:3n-3 increased fatty acid oxidation activity in the liver. These two dietary octadecatrienoic acids differ considerably, however, in how they affect individual fatty acid oxidation enzymes.
据报道,n-3和n-6十八碳三烯酸均可提高肝脏脂肪酸氧化活性。然而,脂肪酸氧化过程中的不同酶对n-3和n-6十八碳三烯酸是否有相似反应仍不清楚。因此,在本研究中,将喂食富含α-亚麻酸(18:3n-3)的油混合物和富含γ-亚麻酸(18:3n-6)的琉璃苣油的大鼠肝脏脂肪酸氧化酶活性,与喂食富含亚油酸(18:2n-6)的油混合物和饱和脂肪(棕榈油)的大鼠进行了比较。亚麻籽油作为富含该十八碳三烯酸的油混合物中18:3n-3的来源,含有30.6%的18:3n-3,但不含18:3n-6。琉璃苣油含有25.7%的18:3n-6和4.5%的18:3n-3。每组7只大鼠,喂食含15%不同脂肪的日粮15天。喂食富含18:3n-3的脂肪混合物(3.03 nmol/分钟/毫克蛋白质)和琉璃苣油(2.89 nmol/分钟/毫克蛋白质)的大鼠,其过氧化物酶体中棕榈酰辅酶A的氧化速率高于喂食棕榈油(2.08 nmol/分钟/毫克蛋白质)和富含18:2n-6的脂肪混合物(2.15 nmol/分钟/毫克蛋白质)的大鼠。喂食富含18:3n-3的脂肪混合物的大鼠线粒体棕榈酰辅酶A氧化速率最高(1.93 nmol/分钟/毫克蛋白质),但其他组之间该参数无显著差异(1.25 - 1.46 nmol/分钟/毫克蛋白质)。与棕榈油和富含18:2n-6的脂肪混合物相比,富含18:3n-3的脂肪混合物和琉璃苣油显著提高了肉碱棕榈酰转移酶和酰基辅酶A氧化酶的肝脏活性。与棕榈油和富含18:2n-6的脂肪混合物相比,富含18:3n-3的脂肪混合物显著降低了3-羟基酰基辅酶A脱氢酶活性,但富含18:3n-6的脂肪则没有。与棕榈油和富含18:2n-6的脂肪混合物相比,琉璃苣油显著降低了线粒体酰基辅酶A脱氢酶活性,但富含18:3n-3的脂肪混合物则提高了该活性。喂食棕榈油的大鼠2,4-二烯酰辅酶A还原酶活性显著低于其他组。与其他脂肪相比,琉璃苣油显著提高了δ3,δ2-烯酰辅酶A异构酶活性。喂食18:2n-6油的大鼠该活性也显著高于喂食棕榈油的大鼠。已证实日粮中的18:3n-6和18:3n-3均可提高肝脏脂肪酸氧化活性。然而,这两种日粮十八碳三烯酸对个体脂肪酸氧化酶的影响差异很大。