Howie A, Huang Y S, Horrobin D F
Efamol Research Institute, Kentville, N.S., Canada.
Biochem Cell Biol. 1992 Aug;70(8):643-9. doi: 10.1139/o92-099.
Effects of supplementation of growth-promoting cholesterol on metabolism of the cytotoxic (n - 6) polyunsaturated fatty acids in cultured human monocyte-like cells (U937) have been examined. U937 cells were incubated in 5% delipidated fetal bovine serum containing 0 or 38.7 microM cholesterol. The rate of uptake and the distribution of metabolites of (n - 6) fatty acids (such as 18:2(n - 6), 18:3(n - 6), and 20:3(n - 6), and 20:4(n - 6)) were examined by adding radiolabelled fatty acid at a level of 1 microgram/mL (3.3 microM for 20-carbon fatty acids and 3.6 microM for 18-carbon-fatty acids). For assessing the cytotoxicity, (n - 6) fatty acids were added to medium at a concentration of 5 micrograms/mL (16.4 microM for 20-carbon fatty acids and 17.9 microM for 18-carbon fatty acids). Cholesterol supplementation suppressed the uptake of all (n - 6) fatty acids and reduced the cytotoxic effects of 18:2(n - 6), 20:3(n - 6), and 20:4(n - 6), but not 18:3(n - 6). In addition, cholesterol supplementation increased peroxide production and metabolism of (n - 6) fatty acids in U937 cells. Thus, the differential suppressive effect of cholesterol on the cytotoxicity of different fatty acids could not be attributed to an inhibitory effect on fatty acid delta 6- and delta 5-desaturation, or to an antioxidant effect on peroxide formation.
已研究了添加促生长胆固醇对培养的人单核细胞样细胞(U937)中细胞毒性(n - 6)多不饱和脂肪酸代谢的影响。将U937细胞在含有0或38.7微摩尔胆固醇的5%脱脂胎牛血清中孵育。通过添加1微克/毫升(20碳脂肪酸为3.3微摩尔,18碳脂肪酸为3.6微摩尔)的放射性标记脂肪酸,检测(n - 6)脂肪酸(如18:2(n - 6)、18:3(n - 6)、20:3(n - 6)和20:4(n - 6))的摄取速率和代谢物分布。为评估细胞毒性,将(n - 6)脂肪酸以5微克/毫升(20碳脂肪酸为16.4微摩尔,18碳脂肪酸为17.9微摩尔)的浓度添加到培养基中。添加胆固醇会抑制所有(n - 6)脂肪酸的摄取,并降低18:2(n - 6)、20:3(n - 6)和20:4(n - 6)的细胞毒性作用,但对18:3(n - 6)无影响。此外,添加胆固醇会增加U937细胞中过氧化物的产生和(n - 6)脂肪酸的代谢。因此,胆固醇对不同脂肪酸细胞毒性的差异抑制作用不能归因于对脂肪酸δ6 - 和δ5 - 去饱和的抑制作用,也不能归因于对过氧化物形成的抗氧化作用。