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甜菊糖苷和甜菊醇在肠道细胞中的特异性免疫调节和分泌活性。

Specific immunomodulatory and secretory activities of stevioside and steviol in intestinal cells.

作者信息

Boonkaewwan Chaiwat, Ao Mei, Toskulkao Chaivat, Rao Mrinalini C

机构信息

Department of Physiology, Faculty of Science, Mahidol University, Bangkok 10400, Thailand.

出版信息

J Agric Food Chem. 2008 May 28;56(10):3777-84. doi: 10.1021/jf072681o.

Abstract

Stevioside, isolated from Stevia rebaudiana, is a commercial sweetener. It was previously demonstrated that stevioside attenuates NF-kappaB-dependent TNF-alpha and IL-1beta synthesis in LPS-stimulated monocytes. The present study examined the effects of stevioside and its metabolite, steviol, on human colon carcinoma cell lines. High concentrations of stevioside (2-5 mM) and steviol (0.2-0.8 mM) decreased cell viability in T84, Caco-2, and HT29 cells. Stevioside (2 mM) potentiated TNF-alpha-mediated IL-8 release in T84 cells. However, steviol (0.01-0.2 mM) significantly suppressed TNF-alpha-induced IL-8 release in all three cell lines. In T84 cells, steviol attenuated TNF-alpha-stimulated IkappaB --> NF-kappaB signaling. Chloride transport was stimulated by steviol (0.1 mM) > stevioside (1 mM) at 30 min. Two biological effects of steviol in the colon are demonstrated for the first time: stimulation of Cl(-) secretion and attenuation of TNF-alpha-stimulated IL-8 production. The immunomodulatory effects of steviol appear to involve NF-kappaB signaling. In contrast, at nontoxic concentrations stevioside affects only Cl(-) secretion.

摘要

从甜叶菊中分离出的甜菊糖苷是一种商业甜味剂。先前有研究表明,甜菊糖苷可减弱脂多糖刺激的单核细胞中依赖核因子κB的肿瘤坏死因子-α和白细胞介素-1β的合成。本研究检测了甜菊糖苷及其代谢产物甜菊醇对人结肠癌细胞系的影响。高浓度的甜菊糖苷(2 - 5 mM)和甜菊醇(0.2 - 0.8 mM)可降低T84、Caco - 2和HT29细胞的活力。甜菊糖苷(2 mM)可增强T84细胞中肿瘤坏死因子-α介导的白细胞介素-8释放。然而,甜菊醇(0.01 - 0.2 mM)在所有三种细胞系中均显著抑制肿瘤坏死因子-α诱导的白细胞介素-8释放。在T84细胞中,甜菊醇减弱了肿瘤坏死因子-α刺激的IκB向核因子κB的信号传导。30分钟时,甜菊醇(0.1 mM)比甜菊糖苷(1 mM)更能刺激氯离子转运。首次证明了甜菊醇在结肠中的两种生物学效应:刺激氯离子分泌和减弱肿瘤坏死因子-α刺激的白细胞介素-8产生。甜菊醇的免疫调节作用似乎涉及核因子κB信号传导。相比之下,在无毒浓度下,甜菊糖苷仅影响氯离子分泌。

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