Lahat A, Ben-Horin S, Lang A, Fudim E, Picard O, Chowers Y
Department of Gastroenterology, Chaim Sheba Medical Center affiliated with the Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Clin Exp Immunol. 2008 May;152(2):320-7. doi: 10.1111/j.1365-2249.2008.03636.x. Epub 2008 Mar 18.
Lidocaine is a commonly used local anaesthetic agent which has also been found to possess anti-inflammatory activity in several disorders. However, the mechanism of this effect has been little explored. The aim of this study was to investigate the effect of lidocaine on stimulated human T cells. The effect of lidocaine on Jurkat T cells was examined by enzyme-linked immunosorbent assay (ELISA) to determine secretion of interleukin (IL)-2, and by the [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] viability assay. Tumour necrosis factor (TNF)-alpha and IL-2 mRNA expression was determined by reverse transcription-polymerase chain reaction. In addition, the effect of lidocaine on the proliferation of freshly isolated peripheral blood (PB) CD3(+) T cells was examined by carboxyfluorescein succinimidyl ester dilution. Apoptosis induction and cytokine production and secretion were determined by annexin V/PI assay, intracellular immunostaining and ELISA respectively. The results showed that lidocaine exerts a dose-dependent inhibition of IL-2 and TNF-alpha secretion by Jurkat T cells at the protein and mRNA levels. Moreover, lidocaine reduced nuclear factor-kappaB (NF-kappaB) signalling in clinically relevant concentrations. Similarly, proliferation of anti-CD3 stimulated PB T cells was abrogated significantly by lidocaine, and the percentage of interferon-gamma- and TNF-alpha-producing T cells was diminished after culture with this agent. In both experimental systems, lidocaine's effect was not mediated by cytotoxic mechanism, as no significant apoptosis or necrosis was demonstrated following co-culture of T cells with this drug. In conclusion, lidocaine's anti-inflammatory effect may be mediated by a drug-induced abrogation of T cell proliferation and cytokine secretion independent of cell death. These effects are mediated at least partly by inhibition of NF-kappaB signalling.
利多卡因是一种常用的局部麻醉剂,人们还发现它在多种疾病中具有抗炎活性。然而,这种作用的机制鲜有研究。本研究的目的是调查利多卡因对受刺激的人T细胞的影响。通过酶联免疫吸附测定(ELISA)检测利多卡因对Jurkat T细胞的影响,以确定白细胞介素(IL)-2的分泌情况,并通过[3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐]活力测定法进行检测。通过逆转录-聚合酶链反应测定肿瘤坏死因子(TNF)-α和IL-2 mRNA的表达。此外,通过羧基荧光素琥珀酰亚胺酯稀释法检测利多卡因对新鲜分离的外周血(PB)CD3(+) T细胞增殖的影响。分别通过膜联蛋白V/碘化丙啶测定、细胞内免疫染色和ELISA确定凋亡诱导以及细胞因子的产生和分泌情况。结果表明,利多卡因在蛋白质和mRNA水平上对Jurkat T细胞分泌IL-2和TNF-α具有剂量依赖性抑制作用。此外,利多卡因在临床相关浓度下可降低核因子-κB(NF-κB)信号传导。同样,利多卡因可显著抑制抗CD3刺激的PB T细胞的增殖,并且在用该药物培养后,产生干扰素-γ和TNF-α的T细胞百分比降低。在这两个实验系统中,利多卡因的作用不是由细胞毒性机制介导的,因为T细胞与该药物共培养后未显示出明显的凋亡或坏死。总之,利多卡因的抗炎作用可能是由药物诱导的T细胞增殖和细胞因子分泌的废除介导的,与细胞死亡无关。这些作用至少部分是由NF-κB信号传导的抑制介导的。