Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/100409
Author(s): Ana Correia Branco
Claudia F Azevedo
Joao R Araujo
Joao T Guimaraes
Ana Faria
Elisa Keating
Fatima Martel
Title: Xanthohumol impairs glucose uptake by a human first-trimester extravillous trophoblast cell line (HTR-8/SVneo cells) and impacts the process of placentation
Issue Date: 2015
Abstract: In this study, we aimed to investigate modulation of glucose uptake by the HTR-8/SVneo human first-trimester extravillous trophoblast cell line by a series of compounds and to study its consequences upon cell proliferation, viability and migration. We observed that uptake of H-3-deoxy-D-glucose (H-3-DG; 10 nM) was time-dependent, saturable, inhibited by cytochalasin B (50 and 100 mu M), phloretin (0.5 mM) and phloridzin (1 mM), insulin-insensitive and sodium-independent. In the short term (30 min), neither 5-HT (100-1000 mu M), melatonin (10 nM) nor the drugs of abuse ethanol (100 mu M), nicotine (100 mu M), cocaine (25 mu M), amphetamine (10-25 mu M) and 3,4-methylene-dioxy-N-methamphetamine (10 mu M) affected 3H-DG uptake, while dexamethasone (100-1000 mu M), fluoxetine (100-300 mu M), quercetin, epigallocatechin-3-gallate (30-1000 mu M), xanthohumol (XH) and resveratrol (1-500 mu M) decreased it. XH was the most potent inhibitor [IC50 = 3.55 (1.37-9.20) mu M] of H-3-DG uptake, behaving as a non-competitive inhibitor of 3H-DG uptake, both after short-and long-term (24 h) treatment. The effect of XH(5 mu M; 24 h) upon H-3-DG uptake involved mammalian target of rapamycin, tyrosine kinases and c-Jun N-terminal kinases intracellular pathways. Moreover, XH appeared to decrease cellular uptake of lactate due to inhibition of the monocarboxylate transporter 1. Additionally, XH (24 h; 5 mu M) decreased cell viability, proliferation, culture growth and migration. The effects of XH upon cell viability and culture growth, but not the antimigratory effect, were mimicked by low extracellular glucose conditions and reversed by high extracellular glucose conditions. We thus suggest that XH, by inhibiting glucose cellular uptake and impairing HTR-8/SVneo cell viability and proliferation, may have a deleterious impact in the process of placentation.
Subject: Medicina clínica
Clinical medicine
Scientific areas: Ciências médicas e da saúde::Medicina clínica
Medical and Health sciences::Clinical medicine
URI: https://repositorio-aberto.up.pt/handle/10216/100409
Document Type: Artigo em Revista Científica Internacional
Rights: restrictedAccess
Appears in Collections:FCNAUP - Artigo em Revista Científica Internacional

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