Department of Oral Medicine & Diagnostic Sciences, Center for Molecular Biology of Oral Diseases, College of Dentistry, University of Illinois at Chicago, 801 South Paulina Street, Chicago, IL 60612, USA.
Department of Clinical Nutrition, College of Health Sciences, Rush University Medical Center, 600 South Paulina St, Room 716 AAC, Chicago, IL 60612, USA.
Molecules. 2020 Oct 16;25(20):4753. doi: 10.3390/molecules25204753.
Consumption of green tea (GT) and GT polyphenols has prevented a range of cancers in rodents but has had mixed results in humans. Human subjects who drank GT for weeks showed changes in oral microbiome. However, GT-induced changes in RNA in oral epithelium were subject-specific, suggesting GT-induced changes of the oral epithelium occurred but differed across individuals. In contrast, studies in rodents consuming GT polyphenols revealed obvious changes in epithelial gene expression. GT polyphenols are poorly absorbed by digestive tract epithelium. Their metabolism by gut/oral microbial enzymes occurs and can alter absorption and function of these molecules and thus their bioactivity. This might explain the overall lack of consistency in oral epithelium RNA expression changes seen in human subjects who consumed GT. Each human has different gut/oral microbiomes, so they may have different levels of polyphenol-metabolizing bacteria. We speculate the similar gut/oral microbiomes in, for example, mice housed together are responsible for the minimal variance observed in tissue GT responses within a study. The consistency of the tissue response to GT within a rodent study eases the selection of a dose level that affects tumor rates. This leads to the theory that determination of optimal GT doses in a human requires knowledge about the gut/oral microbiome in that human.
饮用绿茶(GT)和 GT 多酚已预防了一系列啮齿动物的癌症,但在人类中的结果却喜忧参半。饮用 GT 数周的人类受试者的口腔微生物组发生了变化。然而,GT 诱导的口腔上皮细胞 RNA 变化具有个体特异性,这表明 GT 诱导的口腔上皮变化发生了,但在个体之间存在差异。相比之下,在摄入 GT 多酚的啮齿动物研究中发现了上皮基因表达的明显变化。GT 多酚被消化道上皮吸收不良。它们在肠道/口腔微生物酶的作用下发生代谢,从而改变这些分子的吸收和功能,进而改变它们的生物活性。这或许可以解释在饮用 GT 的人类受试者中观察到的口腔上皮 RNA 表达变化总体缺乏一致性的原因。每个人的肠道/口腔微生物组都不同,因此他们可能具有不同水平的多酚代谢细菌。我们推测,例如,饲养在一起的小鼠中相似的肠道/口腔微生物组可能是导致研究中组织 GT 反应观察到的最小差异的原因。在啮齿动物研究中,组织对 GT 的反应一致性减轻了选择影响肿瘤发生率的剂量水平的难度。这导致了这样一种理论,即在人类中确定 GT 的最佳剂量需要了解该人类的肠道/口腔微生物组。
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