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Medical Research Council Environmental Epidemiology Unit, University of Southampton, Southampton General Hospital (K.M.G., N.M., C.W.), Southampton, United Kingdom SO16 6YD; the Department of Child Health and School of Biological Sciences, University of Manchester, St. Marys Hospital (J.G., C.P.S.), Manchester, United Kingdom M13 OJH; and the Institute of Human Nutrition, University of Southampton (A.J.), Southampton, United Kingdom SO9 3TU
Address all correspondence and requests for reprints to: Dr. Keith Godfrey, Medical Research Council Environmental Epidemiology Unit, University of Southampton, Southampton General Hospital, Southampton, United Kingdom SO16 6YD. E-mail: kmg{at}mrc.soton.ac.uk
Understanding the physiological regulation of fetal growth is important, as normal variations in size at birth relate to differences in neonatal and adult health. Although fetal growth directly reflects net placental transfer, little is known about how normal fetal growth relates to the transfer capabilities of the placental epithelium, the syncytiotrophoblast. The Na+-dependent and Na+-independent uptakes of methylaminoisobutyric acid (MeAIB) by vesicles prepared from the syncytiotrophoblast microvillous plasma membrane give measurements of system A neutral amino acid transporter activity and diffusive permeability, respectively. In 62 normal pregnancies, we related vesicle MeAIB uptakes to neonatal anthropometry. Smaller babies with a lower abdominal circumference had higher placental system A activity per mg membrane protein (P = 0.004); activity rose from 0.020 to 0.043 nmol/30 sec/mg protein as abdominal circumference fell from 34.6 cm or more to 32.0 cm or less. Within the normal range of fetal and placental size, this may reflect a tendency toward compensatory up-regulation of the placental system A transporter in smaller babies. Babies with a lower abdominal circumference also had higher Na+-independent MeAIB uptakes (P = 0.0005); this could reflect important compositional changes in the microvillous plasma membrane, leading in vivo to increased back-diffusion of amino acids out of the syncytiotrophoblast.
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