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无烟烟草提取物对肿瘤坏死因子-α(TNF-α)和白细胞介素-1β(IL-1β)产生以及淋巴细胞增殖的体外作用。

In vitro effects of smokeless tobacco extract on tumor necrosis factor-alpha (TNF-alpha) and interleukin-1beta (IL-1beta) production, and on lymphocyte proliferation.

作者信息

Seyedroudbari S A, Khan M M

机构信息

Department of Pharmaceutical and Adm Sciences, Creighton University Health Sciences Center, Omaha, NE 68178, USA.

出版信息

Toxicon. 1998 Apr;36(4):631-7. doi: 10.1016/s0041-0101(97)00092-5.

Abstract

The use of smokeless tobacco (moist snuff) products is associated with mucosal lesions, gingival recession, attachment loss, and oral cancer. Despite numerous reports on the general toxic effects of smokeless tobacco extract, little information is available regarding the specific effects of smokeless tobacco on immune response. Inflammatory cytokines released as a result of smokeless tobacco-induced irritation may play a role in the development of oral mucosal lesions at habitual tobacco placement sites in smokeless tobacco users. Consequently, the purpose of this study was to determine whether an aqueous extract of smokeless tobacco (STE) affects the secretion of tumor necrosis factor-alpha (TNF-alpha), interleukin-1beta (IL-1beta), and the proliferation of lymphocytes. A macrophage cell line (J774-A1) was used to measure the effects of STE on tumor necrosis factor-alpha (TNF-alpha) and interleukin-1beta (IL-1beta) secretion. Mouse splenocytes were used to assess the effects of STE on lymphocyte proliferation. We found that STE at low concentrations enhanced the production of both TNF-alpha and IL-1beta. Furthermore, STE at similar concentrations enhanced mitogen-induced murine splenocyte proliferation. Overall, these data suggest that smokeless tobacco upregulated two key proinflammatory cytokines and also induces lymphocyte proliferation.

摘要

使用无烟烟草(湿鼻烟)产品与黏膜病变、牙龈退缩、附着丧失和口腔癌有关。尽管有大量关于无烟烟草提取物一般毒性作用的报道,但关于无烟烟草对免疫反应的具体影响的信息却很少。无烟烟草引起的刺激所释放的炎性细胞因子可能在无烟烟草使用者习惯放置烟草部位的口腔黏膜病变发展中起作用。因此,本研究的目的是确定无烟烟草水提取物(STE)是否会影响肿瘤坏死因子-α(TNF-α)、白细胞介素-1β(IL-1β)的分泌以及淋巴细胞的增殖。使用巨噬细胞系(J774-A1)来测量STE对肿瘤坏死因子-α(TNF-α)和白细胞介素-1β(IL-1β)分泌的影响。使用小鼠脾细胞来评估STE对淋巴细胞增殖的影响。我们发现低浓度的STE会增强TNF-α和IL-1β的产生。此外,类似浓度的STE会增强有丝分裂原诱导的小鼠脾细胞增殖。总体而言,这些数据表明无烟烟草上调了两种关键的促炎细胞因子,并且还诱导淋巴细胞增殖。

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