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Effects of artificial sweeteners on the AhR- and GR-dependent CYP1A1 expression in primary human hepatocytes and human cancer cells
被引:14
|作者:
Kamenickova, Alzbeta
[1
]
Pecova, Michaela
[1
]
Bachleda, Petr
[2
]
Dvorak, Zdenek
[1
]
机构:
[1] Palacky Univ, Dept Cell Biol & Genet, Fac Sci, Olomouc 78371, Czech Republic
[2] Univ Hosp Olomouc, Dept Surg 2, Olomouc 77520, Czech Republic
关键词:
Artificial sweeteners;
Aryl hydrocarbon receptor;
Glucocorticoid receptor;
Cytochrome P450;
Food-drug interactions;
ARYL-HYDROCARBON RECEPTOR;
CYTOCHROMES P450;
CONSTRUCTION;
METABOLISM;
ACTIVATION;
ENZYMES;
LINE;
D O I:
10.1016/j.tiv.2013.10.001
中图分类号:
R99 [毒物学(毒理学)];
学科分类号:
100405 ;
摘要:
Food constituents may cause a phenomenon of food-drug interactions. In the current study, we examined the effects of artificial sweeteners (aspartame, acesulfame, cyclamate, saccharin) on the aryl hydrocarbon receptor (AhR) and glucocorticoid receptor (GR)-dependent expression of CYP1A1 in human hepatocytes, hepatic HepG2 and intestinal LS174T cancer cell lines. Sweeteners were tested in concentrations up to those occurring in non-alcoholic beverages. Basal and ligand-inducible AhR- and GR-dependent reporter gene activation in stably transfected HepG2 and HeLa cells, respectively, were not affected by either of the sweeteners tested after 24 h of incubation. The expression of CYP1A1 mRNA and protein in primary cultures of human hepatocytes and in LS174T and HepG2 cells was not induced by any of the tested sweeteners. Overall, aspartame, acesulfame, saccharin and cyclamate had no effects on CYP1A1 expression and transcriptional activities of AhR and GR. These data imply the safety of artificial sweeteners in terms of interference with AhR, GR and CYP1A1. (C) 2013 Elsevier Ltd. All rights reserved.
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页码:2283 / 2288
页数:6
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