Department of Food and Nutrition, Chungnam National University, Daejeon 305-764, Republic of Korea.
Int Immunopharmacol. 2013 Sep;17(1):123-31. doi: 10.1016/j.intimp.2013.05.013. Epub 2013 Jun 1.
Recently, some endocannabinoids were reported to show anti-inflammatory and anti-allergic activities. In this respect, various arachidonoyl endocannabinoids were screened for the inhibition of allergic response in IgE-activated RBL-2H3 cells. Among arachidonoyl endocannabinoids with a low cytotoxicity, only NA-5HT remarkably inhibited the release of β-hexosaminidase (IC(50), 13.58 μM), a marker of degranulation, and tumor necrosis factor-α (IC(50), 12.52 μM), a pro-inflammatory cytokine, in IgE-activated RBL-2H3 cells. Additionally, NA-5HT markedly suppressed the formation of prostaglandin D(2) (PGD(2)) with IC(50) value of 1.27 μM and leukotriene B(4) (LTB(4)) with IC(50) value of 1.20 μM, and slightly LTC4. When effect of NA-5HT on early stage of FcεRI cascade was investigated, it significantly inhibited phosphorylation of Syk, but not Lyn. Furthermore, NA-5HT suppressed phosphorylation of PLCγ1/2 and PKCδ, related to degranulation process, as well as phosphorylation of LAT, ERK1/2, p38, JNK, Gab2, PI3K and Akt, implicated in the expression of pro-inflammatory cytokines. Relative to its effect on the late stage, NA-5HT slightly reduced phosphorylation of 5-lipoxygenase (5-LO) and cyclooxygenase-2 (COX-2). Additionally, NA-5HT significantly reduced the level of p40(phox), and partially inhibited the expression of p47(phox) and p67(phox). From these results, it is suggested that NA-5HT expresses anti-allergic action by suppressing the activation of Syk, LAT, p38, JNK, PI3K and Akt, as well as the expression of ERK1/2 and NADPH oxidase subunits. Further, a strong inhibition of PGD(2) or LTB(4) biosynthesis by NA-5HT may be an additional mechanism for its anti-allergic action. Such anti-allergic actions of NA-5HT may contribute to further information about its biological functions.
最近,有研究报道一些内源性大麻素具有抗炎和抗过敏活性。在这方面,我们筛选了各种花生四烯酰基内源性大麻素,以抑制 IgE 激活的 RBL-2H3 细胞中的过敏反应。在具有低细胞毒性的花生四烯酰基内源性大麻素中,只有 NA-5HT 显著抑制了β-己糖胺酶(IC50,13.58 μM)的释放,β-己糖胺酶是脱粒的标志物,以及肿瘤坏死因子-α(IC50,12.52 μM),一种促炎细胞因子,在 IgE 激活的 RBL-2H3 细胞中。此外,NA-5HT 显著抑制前列腺素 D2(PGD2)的形成,IC50值为 1.27 μM,白三烯 B4(LTB4)的 IC50值为 1.20 μM,LTC4 略有减少。当研究 NA-5HT 对 FcεRI 级联反应早期阶段的影响时,它显著抑制了 Syk 的磷酸化,但不抑制 Lyn 的磷酸化。此外,NA-5HT 抑制了与脱粒过程相关的 PLCγ1/2 和 PKCδ的磷酸化,以及与促炎细胞因子表达相关的 LAT、ERK1/2、p38、JNK、Gab2、PI3K 和 Akt 的磷酸化。与对晚期的影响相比,NA-5HT 轻微降低了 5-脂氧合酶(5-LO)和环氧化酶-2(COX-2)的磷酸化。此外,NA-5HT 显著降低了 p40(phox)的水平,并部分抑制了 p47(phox)和 p67(phox)的表达。从这些结果可以看出,NA-5HT 通过抑制 Syk、LAT、p38、JNK、PI3K 和 Akt 的激活以及 ERK1/2 和 NADPH 氧化酶亚基的表达来表达抗过敏作用。此外,NA-5HT 对 PGD2或 LTB4生物合成的强烈抑制可能是其抗过敏作用的另一个机制。NA-5HT 的这种抗过敏作用可能有助于进一步了解其生物学功能。