Differential effects of nicotine and aging on splenocyte proliferation and the production of Th1- versus Th2-type cytokines.

N. Hallquist, A. Hakki, L. Wecker, H. Friedman, S. Pross
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引用次数: 44

Abstract

Nicotine has a multitude of biological actions in the central and peripheral nervous systems where nicotinic acetylcholine receptors are found. Nicotinic acetylcholine receptors have also been identified on immune cells, but the effects of nicotine on immune responses are not well characterized. These studies tested the hypotheses that nicotine has an effect on both T-lymphocyte proliferation and the production of cytokines by activated T cells, processes that are necessary for effective T-cell-mediated immune responses. In addition, the effects of nicotine on these immune responses in aging animals and the effects of nicotine exposure prior to immunostimulation were investigated. Murine splenocytes were exposed to nicotine and stimulated with concanavalin A (ConA). The highest concentration of nicotine (128 microg/ml) significantly depressed proliferation of T cells both when nicotine and ConA were added concurrently and when nicotine was added 3 hr prior to ConA. Nicotine, added concurrently with ConA at concentrations between 0. 25 and 64 microg/ml, significantly inhibited the production of IL-10 by splenocytes from young adult mice, whereas the inhibition of production of IL-10 by splenocytes from old mice was significantly inhibited, but the response was more variable, depending on the nicotine concentration. In contrast, the production of IFN-gamma by splenocytes from either young adult or old mice was not affected when nicotine (0.016-64 microg/ml) was added concurrently with ConA. Pre-exposure to 1 microg/ml of nicotine for 3 hr significantly enhanced the production of IFN-gamma by splenocytes from young adult mice, whereas pre-exposure to 0.016 microg/ml of nicotine tended to but did not significantly enhance IFN-gamma production. Nicotine is now being used as an over-the-counter drug by people who differ in age and general immunocompetence. Therefore, the effects of nicotine on immune responses, independent from the effects of the other chemicals found in tobacco, need to be investigated.
尼古丁和衰老对脾细胞增殖和Th1-与th2型细胞因子产生的不同影响。
尼古丁在中枢和周围神经系统中有多种生物作用,其中尼古丁乙酰胆碱受体被发现。在免疫细胞上也发现了尼古丁乙酰胆碱受体,但尼古丁对免疫反应的影响尚不清楚。这些研究测试了尼古丁对T淋巴细胞增殖和激活T细胞产生细胞因子的影响的假设,这些过程是有效的T细胞介导的免疫反应所必需的。此外,研究了尼古丁对衰老动物免疫反应的影响以及免疫刺激前尼古丁暴露的影响。小鼠脾细胞暴露于尼古丁和康那霉素A (ConA)刺激。最高浓度的尼古丁(128微克/毫升)在尼古丁和ConA同时添加以及在ConA前3小时添加时均显著抑制T细胞的增殖。尼古丁,与ConA同时添加,浓度在0。25和64 μ g/ml均能显著抑制年轻成年小鼠脾细胞产生IL-10,而对老年小鼠脾细胞产生IL-10的抑制作用则被显著抑制,但反应的差异较大,取决于尼古丁浓度。相比之下,当尼古丁(0.016-64微克/毫升)与ConA同时添加时,青年或老年小鼠脾细胞产生ifn - γ不受影响。预暴露于1微克/毫升尼古丁3小时显著提高了年轻成年小鼠脾细胞ifn - γ的产生,而预暴露于0.016微克/毫升尼古丁倾向于但没有显著提高ifn - γ的产生。尼古丁现在作为一种非处方药被不同年龄和一般免疫能力的人使用。因此,尼古丁对免疫反应的影响,独立于烟草中发现的其他化学物质的影响,需要进行研究。
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