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In vitro effects of eicosanoids derived from different 20-carbon Fatty acids on production of monocyte-derived cytokines in human whole blood cultures.

机译:源自不同20碳脂肪酸的类花生酸对人全血培养物中单核细胞衍生细胞因子产生的体外影响。

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Introduction Prostaglandins (PG) and leukotrienes (LT) are usually formed from arachidonic acid (e.g. PGE(2), LTB(4), LTC(4)). The anti-inflammatory effects of fish oil may be mediated through the production of alternative PG and/or LT formed from eicosapentaenoic acid (e.g. PGE(3), LTC(5)). This study examines the effects of PG and LT derived from different fatty acid precursors on lipopolysaccharide-induced cytokine production by cultured human whole blood.Methods Human whole blood was diluted 1:5 and incubated for 48h with lipopolysaccharide. PGE and LT were added and the concentrations of inflammatory cytokines in the cell culture supernatants determined.Results Tumour necrosis factor (TNF)-alpha concentrations were significantly decreased by the addition of PGE. At the maximum concentration used (10(-6)M) TNF-alpha concentration was reduced to 100%, 90% and 70% by PGE(1), PGE(2) and PGE(3) respectively. Likewise, interleukin (IL)-1beta concentration was decreased to 60%, 30% and 40% by 10(-6)M PGE(1), PGE(2) and PGE(3), respectively. IL-6 and IL-10 concentrations were not altered by PG. LTB(4), LTC(4) or LTC(5) did not significantly affect cytokine concentrations.Conclusions PGE inhibit lipopolysaccharide-stimulated TNF-alpha and IL-1beta production in human whole blood cultures. PGE(1), PGE(2) and PGE(3) show a similar pattern and magnitude of effect. This suggests that the anti-inflammatory effects of dietary fish oil may not be mediated through a simple substitution of one family of eicosanoids for another.
机译:简介前列腺素(PG)和白三烯(LT)通常由花生四烯酸形成(例如PGE(2),LTB(4),LTC(4))。鱼油的抗炎作用可以通过产生二十碳五烯酸(例如PGE(3),LTC(5))形成的替代PG和/或LT介导。本研究探讨了不同脂肪酸前体的PG和LT对人全血培养产生的脂多糖诱导的细胞因子的影响。方法将人全血以1:5的比例稀释,并与脂多糖孵育48小时。加入PGE和LT,测定细胞培养上清中炎性细胞因子的浓度。结果加入PGE可显着降低肿瘤坏死因子(TNF)-α的浓度。在最大使用浓度(10(-6)M)下,PGE(1),PGE(2)和PGE(3)分别将TNF-α浓度降低至100%,90%和70%。同样,白介素(IL)-1beta浓度分别通过10(-6)M PGE(1),PGE(2)和PGE(3)降至60%,30%和40%。 PG不会改变IL-6和IL-10的浓度。 LTB(4),LTC(4)或LTC(5)不会显着影响细胞因子的浓度。结论PGE抑制人全血培养物中脂多糖刺激的TNF-α和IL-1beta的产生。 PGE(1),PGE(2)和PGE(3)显示出相似的效果模式和幅度。这表明食用鱼油的抗炎作用可能不会通过一个类花生酸类的简单替代而被介导。

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