Abstract
Background:
Norepinephrine (NE) and epinephrine (EPI) levels are higher in cord arterial blood relative to venous blood, consistent with active mechanisms of placental-maternal clearance. There are no contemporary studies of cord arteriovenous blood levels of sulfated and non-sulfated catechols.
Aim:
To assess the arteriovenous differences in cord blood levels of dopamine (DA), the sulfated catecholamines and their sulfated and non-sulfated metabolites. To correlate levels of oxygen, H+/CO2, and glucose with cord catecholamine levels.
Methods:
Fifty-seven term infants, delivered by elective cesarean section, were recruited. Cord arterial and venous blood was sampled; levels of glucose, lactate, blood gases, six catechols and their sulfated conjugates were measured.
Results:
With one exception (DOPA sulfate), mean cord arterial levels of sulfated and non-sulfated catechols were significantly higher than venous levels. Arterial lactate and glucose levels were independently associated with NE levels, but only lactate was associated with levels of EPI and DA.
Conclusion:
This study establishes that in vivo metabolic parameters of hypoxia, respiratory and metabolic acidosis are associated with catecholamine levels, a key relationship for perinatal adaptation and homeostasis, and findings that are consistent with in vitro studies of the regulators of catecholamine secretion.
Contributions to the study: Dr. Williams conceptualized and designed the study, carried out the initial analyses, drafted the initial manuscript, revised the manuscript and approved the final manuscript as submitted. Professor Hume conceptualized and designed the study, revised the manuscript and approved the final manuscript as submitted. Ms. Watson carried out the initial analyses, designed the data collection forms, critically reviewed the manuscript and approved the final manuscript as submitted. Dr. Koh undertook the recruitment and data collection, critically reviewed the manuscript and approved the final manuscript as submitted. Professor Eisenhofer supervised the analysis of catechols, critically reviewed the manuscript, and approved the final manuscript as submitted.
Funding: Anonymous Trust (Dundee), NHS Tayside Acute Division Grant Scheme, NHS Scotland Programme Support Grant.
References
[1] Sperling MA, Ganguli S, Leslie N, Landt K. Fetal-perinatal catecholamine secretion: role in perinatal glucose homeostasis. Am J Physiol Endocrinol Metab. 1984;247:E69–74.10.1152/ajpendo.1984.247.1.E69Search in Google Scholar
[2] Falconer AD, Lake DM. Circumstances influencing umbilical-cord plasma catecholamines at delivery. Br J Obstet Gynaecol. 1982;9:44–49.10.1111/j.1471-0528.1982.tb04633.xSearch in Google Scholar
[3] Padbury JF, Martinez AM. Sympathoadrenal system activity at birth: integration of postnatal adaptation. Semin Perinatol. 1988;12:163–72.Search in Google Scholar
[4] Hirsimäki H, Kero P, Ekblad H, Scheinin M, Saraste M, Erkkola R. Mode of delivery, plasma catecholamines and Doppler-derived cardiac output in healthy term newborn infants. Biol Neonate. 1992;61:285–93.10.1159/000243756Search in Google Scholar
[5] Agata Y, Hiraishi S, Misawa H, Han JH, Oguchi K, Horiguchi Y, et al. Hemodynamic adaptations at birth and neonates delivered vaginally and by cesarean section. Biol Neonate. 1995;86:404–11.10.1159/000244263Search in Google Scholar
[6] Nordström L, Marcus C, Persson B, Shimojo N, Westgren M. Lactate in cord blood and its relationship to pH and catecholamines in spontaneous vaginal deliveries. Early Hum Dev. 1996;46:97–104.10.1016/0378-3782(96)01746-XSearch in Google Scholar
[7] Eliot RJ, Lam BSR, Leake RD, Hobel CJ, Fisher DA. Plasma catecholamine concentrations in infants at birth and during the first 48 hours of life. J Pediatr. 1980;96:311–15.10.1016/S0022-3476(80)80836-5Search in Google Scholar
[8] Li W, Weiyan Z, Yanhui Z. The study of maternal and fetal plasma catecholamines levels during pregnancy and delivery. J Perinat Med. 1999;27:195–8.10.1515/JPM.1999.027Search in Google Scholar
[9] Padbury JF, Ludlow JK, Humme JA, Agata Y. Metabolic clearance and plasma appearance rates of catecholamines in preterm and term fetal sheep. Pediatr Res. 1986;20:992–5.10.1203/00006450-198610000-00020Search in Google Scholar
[10] Ganapathy V, Ramamoorthy S, Leibach FH. Transport and metabolism of monoamines in the human placenta. Trophoblast Res. 1993;7:35–51.10.1016/S0143-4004(05)80281-4Search in Google Scholar
[11] Bzoskie L, Blount L, Kashiwai K, Tseng Y-T, Hay WW Jr, Padbury JF. Placental norepinephrine clearance: in vivo measurement and physiological role. Am J Physiol. 1995;269: E145–9.10.1152/ajpendo.1995.269.1.E145Search in Google Scholar PubMed
[12] Stein H, Oyama K, Martinez A, Chappell B, Padbury J. Plasma epinephrine appearance and clearance rates in fetal and newborn sheep. Am J Physiol. 1993;265:R756–60.10.1152/ajpregu.1993.265.4.R756Search in Google Scholar
[13] Boulton AA, Eisenhofer G. Catecholamine metabolism. From molecular understanding to clinical diagnosis and treatment. Overview. Adv Pharmacol. 1998;42:273–92.Search in Google Scholar
[14] Dousa MK, Tyce GM. Free and conjugated plasma catecholamines, DOPA, and 3-O-Methyldopa in humans and in various animals species. Proc Soc Exp Biol Med. 1988;188:427–34.10.3181/00379727-188-42755Search in Google Scholar
[15] Eisenhofer G, Coughtrie MWH, Goldstein DS. Dopamine sulfate: an enigma resolved: proceedings from the 7th International Conference on Peripheral dopamine. Clin Exp Pharmacol Physiol. 1999;26:S4–26.Search in Google Scholar
[16] Livermore S, Piskuric NA, Buttigieg NAJ, Zhang M, Nurse CA. Low glucose sensitivity and polymodal chemosensing in neonatal rat adrenomedullary chromaffin cells. Am J Physiol Cell Physiol. 2011;301:C1104–15.10.1152/ajpcell.00170.2011Search in Google Scholar
[17] Paulick R, Kastendieck E, Wernze H. Catecholamines in arterial and venous umbilical blood: placental extraction, correlation with fetal hypoxia, and transcutaneous partial oxygen tension. J Perinat Med. 1985;13:31–42.10.1515/jpme.1985.13.1.31Search in Google Scholar
[18] Schwab KO, Breitung B, von Stockhausen HB. Inappropriate secretion of umbilical plasma catecholamines in preterm compared to term neonates. J Perinat Med. 1996;24:373–80.10.1515/jpme.1996.24.4.373Search in Google Scholar
[19] Eisenhofer G, Goldstein DS, Stull R, Keiser HR, Sunderland T, Murphy DL, et al. Simultaneous liquid-chromatographic determination of 3,4-DHPG, catecholamines, and 3,4-DOPA in plasma, and their responses to inhibition of monoamine oxidase. Clin Chem. 1986;32:2030–3.10.1093/clinchem/32.11.2030Search in Google Scholar
[20] Irestedt L, Lagercrantz H, Hjemdahl P, Hägnevik K, Belfrage P. Fetal and maternal plasma catecholamine levels at elective cesarean section under general or epidural anesthesia versus vaginal delivery. Am J Obstet Gynecol. 1982;142:1004–10.10.1016/0002-9378(82)90783-9Search in Google Scholar
[21] Hägnevik K, Faxelius G, Irestedt L, Lagercrantz H, Lundell B, Persson B. Catecholamine surge and metabolic adaptation in the newborn after vaginal delivery and caesarean section. Acta Paediatr Scand. 1984;73:602–9.10.1111/j.1651-2227.1984.tb09982.xSearch in Google Scholar PubMed
[22] Lagercrantz H, Bistoletti P. Catecholamine release in newborn-infant at birth. Pediatr Res. 1977;11:889–93.10.1203/00006450-197708000-00007Search in Google Scholar PubMed
[23] Jackson L, Williams FLR, Burchell A, Coughtrie MWH, Hume R. Plasma catecholamines and the counterregulatory response to hypoglycemia in infants: a critical role for epinephrine and cortisol. J Clin Endocrinol Metab. 2004;89:6251–6.10.1210/jc.2004-0550Search in Google Scholar PubMed
[24] Borta A, Höglinger GU. Dopamine and adult neurogenesis. J Neurochem. 2007;100:587–95.10.1111/j.1471-4159.2006.04241.xSearch in Google Scholar
[25] Melnikova VI, Orosco M, Rouch C, Calas A, Nicolaidïs S, Proshlyakova E, et al. Prolactin secretion and its dopamine inhibitory control in rat fetuses. Eur J Endocrinol. 1998;139:337–42.10.1530/eje.0.1390337Search in Google Scholar
[26] Sarasa M, Climent S. Cardiac differentiation induced by dopamine in undifferentiated cells of early chick embryo. Dev Biol. 1991;148:243–8.10.1016/0012-1606(91)90333-XSearch in Google Scholar
[27] Svennilson J, Aperia A. Dopamine in the developing kidney. Int J Dev Biol. 1999;43:441–3.Search in Google Scholar
[28] Richard K, Hume R, Kaptein E, Stanley E, Visser TJ, Coughtrie MWH. Sulfation of thyroid hormone and dopamine during human development: ontogeny of phenol sulfotransferases and arylsulfatase in liver, lung, and brain. J Clin Endocrinol Metab. 2001;86:2734–42.10.1210/jc.86.6.2734Search in Google Scholar
[29] Ugrumov MV, Saifetyarova JY, Lavrentieva AV, Sapronova AY. Developing brain as an endocrine organ: Secretion of dopamine. Mol Cell Endocrinol. 2012;348:78–86.10.1016/j.mce.2011.07.038Search in Google Scholar PubMed
[30] Kuss E. The fetoplacental unit of primates. Exp Clin Endocrinol. 1994;102:135–65.10.1055/s-0029-1211276Search in Google Scholar PubMed
[31] Alvarez-Buylla R, Alvarez-Buylla ER. Carotid sinus receptors participate in glucose homeostasis. Resp Physiol. 1988;72:347–60.10.1007/978-1-4612-3388-6_45Search in Google Scholar
[32] García-Fernández M, Ortega-Saenz P, Castellano A, Lopez-Barneo J. Mechanisms of low-glucose sensitivity in carotid body glomus cells. Diabetes. 2007;56:2893–900.10.2337/db07-0122Search in Google Scholar PubMed
[33] Stevenson RW, Steiner KE, Connolly CC, Fuchs H, Alberti KGMM, Williams PE, et al. Dose-related effects of epinephrine on glucose production in conscious dogs. Am J Physiol. 1991;260:E363–70.10.1152/ajpendo.1991.260.3.E363Search in Google Scholar PubMed
The authors stated that there are no conflicts of interest regarding the publication of this article.
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