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18β-甘草次酸能有效抑制人 Jurkat T 细胞中的 Kv1.3 钾通道和 T 细胞活化。

18β-Glycyrrhetinic acid potently inhibits Kv1.3 potassium channels and T cell activation in human Jurkat T cells.

机构信息

Ion Channelopathy Research Center, Institute of Cardiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, PR China.

出版信息

J Ethnopharmacol. 2013 Jul 9;148(2):647-54. doi: 10.1016/j.jep.2013.05.022. Epub 2013 May 21.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

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.

AIM OF THE STUDY

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.

MATERIALS AND METHODS

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.

RESULTS

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.

CONCLUSION

18β-GA blocks Kv1.3 channels, which probably involves its anti-inflammatory and immunomodulation effects.

摘要

民族药理学相关性

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。

研究目的

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。

材料和方法

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。

结果

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。

结论

18β-GA 阻断 Kv1.3 通道,这可能与其抗炎和免疫调节作用有关。

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