Does maternal-fetal transfer of creatine occur in pregnant sheep?

Author:

Baharom Syed123,De Matteo Robert2,Ellery Stacey1,Della Gatta Paul4,Bruce Clinton R.4,Kowalski Greg M.4,Hale Nadia1,Dickinson Hayley1,Harding Richard2,Walker David15,Snow Rodney J.4

Affiliation:

1. The Ritchie Centre, Hudson Institute of Medical Research, Clayton, Australia;

2. Department of Anatomy and Developmental Biology, Monash University, Melbourne, Australia;

3. Faculty of Medicine, Universiti Teknologi MARA, Sungai Buloh, Selangor, Malaysia

4. Institute for Physical Activity and Nutrition, Deakin University, Melbourne, Australia;

5. Department of Obstetrics and Gynaecology, Monash University, Melbourne, Australia; and

Abstract

Our aim was to determine the disposition of creatine in ovine pregnancy and whether creatine is transferred across the placenta from mother to fetus. Pregnant ewes received either 1) a continuous intravenous infusion of creatine monohydrate or saline from 122 to 131 days gestation, with maternal and fetal arterial blood and amniotic fluid samples collected daily for creatine analysis and fetal tissues collected at necropsy at 133 days for analysis of creatine content, or 2) a single systemic bolus injection of [13C]creatine monohydrate at 130 days of gestation, with maternal and fetal arterial blood, uterine vein blood, and amniotic fluid samples collected before and for 4 h after injection and analyzed for creatine, creatine isotopic enrichment, and guanidinoacetic acid (GAA; precursor of creatine) concentrations. Presence of the creatine transporter-1 (SLC6A8) and l-arginine:glycine amidinotransferase (AGAT; the enzyme synthesizing GAA) proteins were determined by Western blots of placental cotyledons. The 10-day creatine infusion increased maternal plasma creatine concentration three- to fourfold ( P < 0.05) without significantly changing fetal arterial, amniotic fluid, fetal tissues, or placental creatine content. Maternal arterial 13C enrichment was increased ( P < 0.05) after bolus [13C]creatine injection without change of fetal arterial 13C enrichment. SLC6A8 and AGAT proteins were identified in placental cotyledons, and GAA concentration was significantly higher in uterine vein than maternal artery plasma. Despite the presence of SLC6A8 protein in cotyledons, these results suggest that creatine is not transferred from mother to fetus in near-term sheep and that the ovine utero-placental unit releases GAA into the maternal circulation.

Funder

Department of Health, Australian Government | National Health and Medical Research Council (NHMRC)

Publisher

American Physiological Society

Subject

Physiology (medical),Physiology,Endocrinology, Diabetes and Metabolism

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