Ion Channelopathy Research Center, Institute of Cardiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, PR China.
J Ethnopharmacol. 2013 Jul 9;148(2):647-54. doi: 10.1016/j.jep.2013.05.022. Epub 2013 May 21.
Licorice has been extensively used in traditional medicines for treatment of many diseases, including inflammations and immunological disorders. Recent studies have shown that the anti-inflammatory and immunomodulation activities of licorice have been attributed to its active component, glycyrretinic acid (GA). GA consists of two isoforms, 18α- and 18β-. However, its mechanism remains poorly understood.
We compared the effects of two isoforms on Kv1.3 channels in Jurkat T cells and further characterized the inhibition of Kv1.3 channels by 18β-GA in CHO cells. In addition, we examined the effects of 18β-GA on Kv1.3 gene expression, Ca(2+) influx, proliferation, as well as IL-2 production in Jurkat T cells.
Whole-cell patch-clamp technique was applied to record Kv1.3 currents in Jurkat T or CHO cells. Real-time PCR and Western blotting were used to detect gene expression. Fluo-4, CCK-8 kit and ELISA kit were used to measure Ca(2+) influx, proliferation, and IL-2 secretion in Jurkat T cells, respectively.
Superfusion of 18β-GA (10-100 µM) blocked Kv1.3 currents in Jurkat T cells, while 18α-GA at the same concentration had no effect. The 18β-GA induced inhibition had a voltage- and concentration-dependent manner with an IC50 of 23.9±1.5 µM at +40 mV in CHO cells. Furthermore, 18β-GA significantly inhibited Kv1.3 gene expression. In addition, paralleling Kv1.3 inhibition, 18β-GA also inhibited Ca(2+) influx, proliferation as well as IL-2 production in Jurkat T cells.
18β-GA blocks Kv1.3 channels, which probably involves its anti-inflammatory and immunomodulation effects.
甘草在传统医学中被广泛用于治疗许多疾病,包括炎症和免疫紊乱。最近的研究表明,甘草的抗炎和免疫调节活性归因于其活性成分甘草次酸(GA)。GA 由两种异构体,18α-和 18β-组成。然而,其机制仍知之甚少。
我们比较了两种异构体对 Jurkat T 细胞中 Kv1.3 通道的影响,并进一步研究了 18β-GA 在 CHO 细胞中对 Kv1.3 通道的抑制作用。此外,我们还研究了 18β-GA 对 Jurkat T 细胞中 Kv1.3 基因表达、Ca(2+)内流、增殖以及 IL-2 产生的影响。
采用全细胞膜片钳技术记录 Jurkat T 或 CHO 细胞中的 Kv1.3 电流。实时 PCR 和 Western blot 用于检测基因表达。Fluo-4、CCK-8 试剂盒和 ELISA 试剂盒分别用于测量 Jurkat T 细胞中的 Ca(2+)内流、增殖和 IL-2 分泌。
18β-GA(10-100 μM)灌流可阻断 Jurkat T 细胞中的 Kv1.3 电流,而相同浓度的 18α-GA 则没有作用。18β-GA 诱导的抑制作用具有电压和浓度依赖性,在 CHO 细胞中+40 mV 时的 IC50 为 23.9±1.5 μM。此外,18β-GA 显著抑制 Kv1.3 基因表达。此外,与 Kv1.3 抑制平行,18β-GA 还抑制 Jurkat T 细胞中的 Ca(2+)内流、增殖和 IL-2 产生。
18β-GA 阻断 Kv1.3 通道,这可能与其抗炎和免疫调节作用有关。