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Catechins Variously Affect Activities of Conjugation Enzymes in Proliferating and Differentiated Caco-2 Cells

机译:儿茶素对增殖和分化的Caco-2细胞中结合酶活性的不同影响。

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摘要

The knowledge of processes in intestinal cells is essential, as most xenobiotics come into contact with the small intestine first. Caco-2 cells are human colorectal adenocarcinoma that once differentiated, exhibit enterocyte-like characteristics. Our study compares activities and expressions of important conjugation enzymes and their modulation by green tea extract (GTE) and epigallocatechin gallate (EGCG) using both proliferating (P) and differentiated (D) caco-2 cells. The mRNA levels of the main conjugation enzymes were significantly elevated after the differentiation of Caco-2 cells. However, no increase in conjugation enzymes’ activities in differentiated cells was detected in comparison to proliferating ones. GTE/EGCG treatment did not affect the mRNA levels of any of the conjugation enzymes tested in either type of cells. Concerning conjugation enzymes activities, GTE/EGCG treatment elevated glutathione S-transferase (GST) activity by approx. 30% and inhibited catechol-O-methyltransferase (COMT) activity by approx. 20% in differentiated cells. On the other hand, GTE as well as EGCG treatment did not significantly affect the activities of conjugation enzymes in proliferating cells. Administration of GTE/EGCG mediated only mild changes of GST and COMT activities in enterocyte-like cells, indicating a low risk of GTE/EGCG interactions with concomitantly administered drugs. However, a considerable chemo-protective effect of GTE via the pronounced induction of detoxifying enzymes cannot be expected as well.
机译:肠道细胞过程的知识是必不可少的,因为大多数异生物素都首先与小肠接触。 Caco-2细胞是人类大肠腺癌,一旦分化,便表现出肠样细胞特征。我们的研究比较了使用增殖(P)和分化(D)caco-2细胞的绿茶提取物(GTE)和表没食子儿茶素没食子酸酯(EGCG)对重要缀合酶的活性和表达及其调控。 Caco-2细胞分化后,主要结合酶的mRNA水平明显升高。然而,与增殖细胞相比,在分化细胞中未发现缀合酶活性的增加。 GTE / EGCG处理不会影响任何一种细胞中测试的任何结合酶的mRNA水平。关于缀合酶的活性,GTE / EGCG处理可将谷胱甘肽S-转移酶(GST)活性提高约5%。 30%并抑制了邻苯二酚-O-甲基转移酶(COMT)活性。在分化细胞中占20%。另一方面,GTE和EGCG处理并未显着影响增殖细胞中缀合酶的活性。 GTE / EGCG的施用仅介导肠样细胞中GST和COMT活性的轻度变化,表明GTE / EGCG与伴随给药的药物发生相互作用的风险较低。然而,也不能预期通过明显诱导解毒酶而引起的GTE的显着化学保护作用。

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