Kawasaki M, Toyoda M, Teshima R, Sawada J, Saito Y
National Institute of Health Sciences, Tokyo, Japan.
Biol Pharm Bull. 1994 Oct;17(10):1321-5. doi: 10.1248/bpb.17.1321.
We examined the effect of alpha-linolenic acid (18:3 (n-3)) pretreatment on the metabolism of omega-3 and omega-6 polyunsaturated fatty acids and histamine content and release of RBL-2H3 cells. RBL-2H3 cells grew without reduction in number when incubated with subculture media for 3 d and then placed again in serum-free medium with bovine serum albumin (BSA) and epidermal growth factor (EGF). Cholesterol pullulan (10 micrograms/ml) emulsified alpha-linolenic acid (20 micrograms/ml) was recommended as an additional form serum free medium. We determined the fatty acid composition in all neutral lipids, free fatty acids and all phospholipids in alpha-linolenic acid-treated cells. In all cases the concentration of alpha-linolenic acid and docosahexenoic acid (DHA, 22:6 (n-3)) was increased, while linolenic acid (18:2 (n-6)) was slightly and arachidonic acid (20:4 (n-6)) was markedly decreased. Content of histamine in alpha-linolenic acid-treated cells was remarkably lower than that of untreated cells. Accordingly, net histamine release stimulated by antigen or A23187 was also markedly decreased in the alpha-linolenic acid-treated cells, as was the percent histamine release stimulated by antigen. Results from our in vitro experiment suggest that the anti-allergic effect of alpha-linolenic acid may be caused either by the decrease in histamine content or by inhibition of the release of chemical mediator resulting from changes in the fatty acid composition.
我们研究了α-亚麻酸(18:3 (n-3))预处理对ω-3和ω-6多不饱和脂肪酸代谢、组胺含量以及RBL-2H3细胞释放的影响。将RBL-2H3细胞与传代培养基一起孵育3天,然后再次置于含有牛血清白蛋白(BSA)和表皮生长因子(EGF)的无血清培养基中,细胞数量未减少。推荐使用胆固醇普鲁兰多糖(10微克/毫升)乳化的α-亚麻酸(20微克/毫升)作为无血清培养基的一种添加形式。我们测定了α-亚麻酸处理细胞中所有中性脂质、游离脂肪酸和所有磷脂中的脂肪酸组成。在所有情况下,α-亚麻酸和二十二碳六烯酸(DHA,22:6 (n-3))的浓度均升高,而亚油酸(18:2 (n-6))略有下降,花生四烯酸(20:4 (n-6))显著下降。α-亚麻酸处理细胞中的组胺含量明显低于未处理细胞。因此,α-亚麻酸处理细胞中由抗原或A23187刺激的组胺净释放也显著降低,抗原刺激的组胺释放百分比也是如此。我们的体外实验结果表明,α-亚麻酸的抗过敏作用可能是由于组胺含量降低或脂肪酸组成变化导致化学介质释放受到抑制引起的。