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Does maternal-fetal transfer of creatine occur in pregnant sheep?
Baharom, Syed; De Matteo, Robert; Ellery, Stacey; Della Gatta, Paul; Bruce, Clinton R; Kowalski, Greg M; Hale, Nadia; Dickinson, Hayley; Harding, Richard; Walker, David; Snow, Rodney J.
Afiliação
  • Baharom S; The Ritchie Centre, Hudson Institute of Medical Research, Clayton, Australia.
  • De Matteo R; Department of Anatomy and Developmental Biology, Monash University, Melbourne, Australia.
  • Ellery S; Faculty of Medicine, Universiti Teknologi MARA, Sungai Buloh, Selangor, Malaysia.
  • Della Gatta P; Department of Anatomy and Developmental Biology, Monash University, Melbourne, Australia.
  • Bruce CR; The Ritchie Centre, Hudson Institute of Medical Research, Clayton, Australia.
  • Kowalski GM; Institute for Physical Activity and Nutrition, Deakin University, Melbourne, Australia.
  • Hale N; Institute for Physical Activity and Nutrition, Deakin University, Melbourne, Australia.
  • Dickinson H; Institute for Physical Activity and Nutrition, Deakin University, Melbourne, Australia.
  • Harding R; The Ritchie Centre, Hudson Institute of Medical Research, Clayton, Australia.
  • Walker D; The Ritchie Centre, Hudson Institute of Medical Research, Clayton, Australia.
  • Snow RJ; Department of Anatomy and Developmental Biology, Monash University, Melbourne, Australia.
Am J Physiol Endocrinol Metab ; 313(1): E75-E83, 2017 07 01.
Article em En | MEDLINE | ID: mdl-28325734
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-arginineglycine 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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Placenta / Prenhez / Ovinos / Creatina / Glicina / Troca Materno-Fetal Limite: Animals / Pregnancy Idioma: En Revista: Am J Physiol Endocrinol Metab Assunto da revista: ENDOCRINOLOGIA / FISIOLOGIA / METABOLISMO Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Placenta / Prenhez / Ovinos / Creatina / Glicina / Troca Materno-Fetal Limite: Animals / Pregnancy Idioma: En Revista: Am J Physiol Endocrinol Metab Assunto da revista: ENDOCRINOLOGIA / FISIOLOGIA / METABOLISMO Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Austrália