CC BY-NC-ND 4.0 · AJP Rep 2019; 09(02): e177-e184
DOI: 10.1055/s-0039-1692196
Original Article
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Oxytocin and Oxytocinase in the Obese and Nonobese Parturients during Induction and Augmentation of Labor

Annemaria De Tina
1   Department of Anesthesiology, Perioperative and Pain Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts
2   Department of Anesthesiology, McMaster University, Hamilton, Ontario, Canada
,
Jeremy Juang
1   Department of Anesthesiology, Perioperative and Pain Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts
3   Department of Anesthesiology, Massachusetts Eye and Ear Infirmary, Boston, Massachusetts
,
Thomas F. McElrath
4   Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts
,
Jack D. Baty
5   Division of Biostatistics, Washington University School of Medicine, St. Louis, Missouri
,
6   Department of Anesthesiology, Washington University School of Medicine, St. Louis, Missouri
› Author Affiliations
Further Information

Publication History

27 January 2019

12 April 2019

Publication Date:
29 May 2019 (online)

Abstract

Objective To investigate differences in oxytocin (OXT) biodistribution between nonobese and obese parturients during labor.

Study Design Patients with body mass index (BMI) of either ≥ 18 ≤ 24.9 kg/m2 (“nonobese”) or ≥ 30 kg/m2 (“obese”) undergoing elective induction of labor were included (N = 25 each). Blood samples were collected at baseline (T0), and 20 minutes after maximal OXT augmentation or adequate uterine contractions (T1) for OXT and oxytocinase assays. A mixed-model repeated-measures analysis of variance was used to test for group versus time interaction and analysis of covariance to detect a difference in OXT level at T1. Data presented as mean ± standard deviation or median (interquartile range), with p < 0.05 considered significant.

Results The mean BMIs (kg/m2) were 22.1 ± 1.6 and 35.9 ± 5.1 in the nonobese and obese groups, respectively. No differences were observed in either the duration of OXT infusion, total dose of OXT, or plasma OXT (pg/mL) either at T0 or T1. However, plasma oxytocinase (ng/mL) was significantly lower at T0 (1.41 [0.67, 3.51] vs. 0.40 [0.29, 1.12]; p = 0.03) in the obese group.

Conclusion We provide preliminary evidence that the disposition of OXT may not be different between obese and nonobese women during labor.

Authors' Contribution

A.D.T.: This author helped design the study, conducted the study, reviewed analysis, wrote, and approved the final article.


J.J.: This author helped conduct the study, reviewed analysis, wrote, and approved the final article.


T.F.M.: This author helped design the study, reviewed analysis, and approved the final article.


J.D.B.: This author performed statistical analysis and approved the final article.


A.P.: This author conceived the study, designed the study, conducted the study, reviewed analysis, wrote, and approved the final article.


Competing Interest

The authors declare no competing interest.


 
  • References

  • 1 Mission JF, Marshall NE, Caughey AB. Pregnancy risks associated with obesity. Obstet Gynecol Clin North Am 2015; 42 (02) 335-353
  • 2 Galtier-Dereure F, Boegner C, Bringer J. Obesity and pregnancy: complications and cost. Am J Clin Nutr 2000; 71 (5, Suppl): 1242S-1248S
  • 3 Fyfe EM, Anderson NH, North RA. , et al; Screening for Pregnancy Endpoints (SCOPE) Consortium. Risk of first-stage and second-stage cesarean delivery by maternal body mass index among nulliparous women in labor at term. Obstet Gynecol 2011; 117 (06) 1315-1322
  • 4 Barau G, Robillard PY, Hulsey TC. , et al. Linear association between maternal pre-pregnancy body mass index and risk of caesarean section in term deliveries. BJOG 2006; 113 (10) 1173-1177
  • 5 Sherrard A, Platt RW, Vallerand D, Usher RH, Zhang X, Kramer MS. Maternal anthropometric risk factors for caesarean delivery before or after onset of labour. BJOG 2007; 114 (09) 1088-1096
  • 6 Leddy MA, Power ML, Schulkin J. The impact of maternal obesity on maternal and fetal health. Rev Obstet Gynecol 2008; 1 (04) 170-178
  • 7 Carlson NS, Hernandez TL, Hurt KJ. Parturition dysfunction in obesity: time to target the pathobiology. Reprod Biol Endocrinol 2015; 13: 135
  • 8 Norman SM, Tuuli MG, Odibo AO, Caughey AB, Roehl KA, Cahill AG. The effects of obesity on the first stage of labor. Obstet Gynecol 2012; 120 (01) 130-135
  • 9 Kominiarek MA, Zhang J, Vanveldhuisen P, Troendle J, Beaver J, Hibbard JU. Contemporary labor patterns: the impact of maternal body mass index. Am J Obstet Gynecol 2011; 205 (03) 244.e1-244.e8
  • 10 Carlson NS, Corwin EJ, Lowe NK. Oxytocin augmentation in spontaneously laboring, nulliparous women: multilevel assessment of maternal BMI and oxytocin dose. Biol Res Nurs 2017; 19 (04) 382-392
  • 11 Cheymol G. Clinical pharmacokinetics of drugs in obesity. An update. Clin Pharmacokinet 1993; 25 (02) 103-114
  • 12 Hanley MJ, Abernethy DR, Greenblatt DJ. Effect of obesity on the pharmacokinetics of drugs in humans. Clin Pharmacokinet 2010; 49 (02) 71-87
  • 13 Gajdosechova L, Krskova K, Segarra AB. , et al. Hypooxytocinaemia in obese Zucker rats relates to oxytocin degradation in liver and adipose tissue. J Endocrinol 2014; 220 (03) 333-343
  • 14 von Elm E, Altman DG, Egger M, Pocock SJ, Gøtzsche PC, Vandenbroucke JP. ; STROBE Initiative. STrengthening the Reporting of OBservational studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies. BMJ 2007; 335 (7624): 806-808
  • 15 Rahm VA, Hallgren A, Högberg H, Hurtig I, Odlind V. Plasma oxytocin levels in women during labor with or without epidural analgesia: a prospective study. Acta Obstet Gynecol Scand 2002; 81 (11) 1033-1039
  • 16 Prevost M, Zelkowitz P, Tulandi T. , et al. Oxytocin in pregnancy and the postpartum: relations to labor and its management. Front Public Health 2014; 2: 1
  • 17 Leake RD, Weitzman RE, Fisher DA. Pharmacokinetics of oxytocin in the human subject. Obstet Gynecol 1980; 56 (06) 701-704
  • 18 Leake RD, Weitzman RE, Glatz TH, Fisher DA. Plasma oxytocin concentrations in men, nonpregnant women, and pregnant women before and during spontaneous labor. J Clin Endocrinol Metab 1981; 53 (04) 730-733
  • 19 Szeto A, McCabe PM, Nation DA. , et al. Evaluation of enzyme immunoassay and radioimmunoassay methods for the measurement of plasma oxytocin. Psychosom Med 2011; 73 (05) 393-400
  • 20 Caruso S, Mauro D, Scalia G, Palermo CI, Rapisarda AMC, Cianci A. Oxytocin plasma levels in orgasmic and anorgasmic women. Gynecol Endocrinol 2018; 34 (01) 69-72
  • 21 Simpson EA, Paukner A, Sclafani V, Kaburu SS, Suomi SJ, Ferrari PF. Acute oxytocin improves memory and gaze following in male but not female nursery-reared infant macaques. Psychopharmacology (Berl) 2017; 234 (03) 497-506
  • 22 Mathur VS, Walker JM. Oxytocinase in plasma and placenta in normal and prolonged labour. BMJ 1968; 3 (5610): 96-97
  • 23 Yamahara N, Nomura S, Suzuki T. , et al. Placental leucine aminopeptidase/oxytocinase in maternal serum and placenta during normal pregnancy. Life Sci 2000; 66 (15) 1401-1410
  • 24 Ito N, Nomura S, Iwase A. , et al. Ultrastructural localization of aminopeptidase A/angiotensinase and placental leucine aminopeptidase/oxytocinase in chorionic villi of human placenta. Early Hum Dev 2003; 71 (01) 29-37
  • 25 Naruki M, Mizutani S, Goto K. , et al. Oxytocin is hydrolyzed by an enzyme in human placenta that is identical to the oxytocinase of pregnancy serum. Peptides 1996; 17 (02) 257-261
  • 26 Oya M, Yoshino M, Mizutani S, Wakabayashi T. The origin of human pregnancy serum oxytocinase. Gynecol Invest 1974; 5 (5-6): 276-283
  • 27 Ferrier BM, Hendrie JM, Branda LA. Plasma oxytocinase: the synthesis and biological properties of the first product of the degradation of oxytocin by this enzyme. Can J Biochem 1974; 52 (01) 60-66
  • 28 Howell KR, Powell TL. Effects of maternal obesity on placental function and fetal development. Reproduction 2017; 153 (03) R97-R108
  • 29 Tsujimoto M, Mizutani S, Adachi H, Kimura M, Nakazato H, Tomoda Y. Identification of human placental leucine aminopeptidase as oxytocinase. Arch Biochem Biophys 1992; 292 (02) 388-392
  • 30 Mizutani S, Sumi S, Oka K. , et al. In vitro degradation of oxytocin by pregnancy serum, placental subcellular fractions and purified placental aminopeptidases. Exp Clin Endocrinol 1985; 86 (03) 310-316