Effects of C18 Fatty Acids on Intracellular Ca2+ Mobilization and Histamine Release in RBL-2H3 Cells

被引:5
|
作者
Kim, Myung Chul [1 ]
Kim, Min Gyu [1 ]
Jo, Young Soo [1 ]
Song, Ho Sun [1 ]
Eom, Tae In [1 ]
Sim, Sang Soo [1 ]
机构
[1] Chung Ang Univ, Coll Pharm, Seoul 156756, South Korea
关键词
Ca2+ mobilization; C18 fatty acids; Histamine release; PLC assay; CORONARY-HEART-DISEASE; CARDIOVASCULAR-DISEASE; DIETARY N-6; MAST-CELLS; RISK; RATIO;
D O I
10.4196/kjpp.2014.18.3.241
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
To investigate the underlying mechanisms of C18 fatty acids (stearic acid, oleic acid, linoleic acid and alpha-linolenic acid) on mast cells, we measured the effect of C18 fatty acids on intracellular Ca2+ mobilization and histamine release in RBL-2H3 mast cells. Stearic acid rapidly increased initial peak of intracellular Ca2+ mobilization, whereas linoleic acid and alpha-linolenic acid gradually increased this mobilization. In the absence of extracellular Ca2+, stearic acid (100 mu M) did not cause any increase of intracellular Ca2+ mobilization. Both linoleic acid and alpha-linolenic acid increased intracellular Ca2+ mobilization, but the increase was smaller than that in the presence of extracellular Ca2+. These results suggest that C18 fatty acid-induced intracellular Ca2+ mobilization is mainly dependent on extracellular Ca2+ influx. Verapamil dose-dependently inhibited stearic acid-induced intracellular Ca2+ mobilization, but did not affect both linoleic acid-and alpha- linolenic acid-induced intracellular Ca2+ mobilization. These data suggest that the underlying mechanism of stearic acid, linoleic acid and alpha-linolenic acid on intracellular Ca2+ mobilization may differ. Linoleic acid and alpha-linolenic acid significantly increased histamine release. Linoleic acid (C18:2: omega -6)-induced intracellular Ca2+ mobilization and histamine release were more prominent than alpha-linolenic acid (C18:3: omega-3). These data support the view that the intake of more alpha-linolenic acid than linoleic acid is useful in preventing inflammation.
引用
收藏
页码:241 / 247
页数:7
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