Effect of fetal growth restriction on system A amino acid transporter activity in the maternal facing plasma membrane of rat syncytiotrophoblast

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    Abstract

    To determine whether reduced maternofetal transfer of neutral amino acids in growth-restricted fetal rats is due to decreased system A transporter activity, we measured Na+-dependent MeAIB uptake by membrane vesicles from placentas of fetuses growth-restricted due to uterine artery ligation and control placentas (sham ligation). Na+-dependent uptake of methylaminoisobutyric acid (MeAIB) was linear over 15-60 s in vesicles from both ligated and sham-ligated sides of the uterus. Na+dependent uptake of MeAIB at 30 s did not differ in paired measurements on vesicles from ligated and sham-ligated horns, 0.063 ± 0.004 versus 0.056 ± 0.005 nmol/mg of vesicle protein. The kinetics of Na+-dependent MeAIB uptake were similar in paired measurements on vesicles from ligated and sham-ligated horns, with overall K(m) = 4.4 ± 0.5 mM and V(max) = 0.93 ± 0.08 nmol/mg vesicle protein per 30 s. Uptake of tracer was inhibited 85-95% by known substrates for the system A amino acid transporter (alanine ≤ serine > MeAIB > glycine = proline). We conclude that the system A transporter is present in the maternal facing plasma membrane of rat syncytiotrophoblast, but that the activity of this system, per mg of vesicle protein, is unaffected in fetal growth restriction induced by a decrease in maternal placental blood flow in late pregnancy.
    Original languageEnglish
    Pages (from-to)325-329
    Number of pages4
    JournalPEDIATRIC RESEARCH
    Volume40
    Issue number2
    Publication statusPublished - Aug 1996

    Keywords

    • metabolism: Amino Acids
    • Animals
    • physiology: Arteries
    • physiology: Biological Transport, Active
    • metabolism: Carrier Proteins
    • metabolism: Cell Membrane
    • Constriction
    • Female
    • metabolism: Fetal Growth Retardation
    • metabolism: Giant Cells
    • Kinetics
    • Liposomes
    • Pregnancy
    • Rats
    • Rats, Sprague-Dawley
    • metabolism: Trophoblasts
    • blood supply: Uterus

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