Literature DB >> 23806338

Oxidative stress decreases uptake of neutral amino acids in a human placental cell line (BeWo cells).

João Ricardo Araújo1, Ana Correia-Branco, Ana Cláudia Pereira, Maria João Pinho, Elisa Keating, Fátima Martel.   

Abstract

Increased oxidative stress (OS) is implicated in the pathophysiology of several pregnancy disorders. We aimed to investigate the effect of tert-butylhydroperoxide (TBHP)-induced OS upon the placental transport of the neutral amino acids L-methionine (L-Met) and L-alanine (L-Ala), by using a human trophoblast cell model (BeWo cells). TBHP reduced both total and Na(+)-independent (14)C-L-Met intracellular steady-state accumulation over time (Amax), by reducing non-system L-mediated uptake - most probably system y(+) - while having no effect on system L. Moreover, TBHP reduced total (14)C-L-Ala Amax through an inhibition of system A. The effect of TBHP upon total, but not system A-mediated, (14)C-L-Ala uptake was dependent upon phosphoinositide 3-kinase (PI3K) and protein kinase C (PKC) activation, and was completely prevented by the polyphenol quercetin. In conclusion, a reduction in placental uptake of neutral amino acids may contribute to the deleterious effects of pregnancy disorders associated with OS.
Copyright © 2013 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  2-amino-2-norbornanecarboxylic acid; A(max); BCH; EGCG; LAT; MeAIB; N-ethylmaleimide; NEM; Na(+)-coupled neutral amino acid transporter; Nutrients; OS; Oxidative stress; Placenta; SNAT; STB; TBHP; Transport; accumulation at steady state; epigallocatechin-3-gallate; k(in); k(out); l-type amino acid transporter; oxidative stress; rate constant for inward transport; rate constant for outward transport; syncytiotrophoblast; tert-butylhydroperoxide; α-(methylamino)isobutyric acid

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Year:  2013        PMID: 23806338     DOI: 10.1016/j.reprotox.2013.06.073

Source DB:  PubMed          Journal:  Reprod Toxicol        ISSN: 0890-6238            Impact factor:   3.143


  11 in total

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10.  Placental Dysfunction Underlies Increased Risk of Fetal Growth Restriction and Stillbirth in Advanced Maternal Age Women.

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