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dc.contributor.authorJones, A.K.
dc.contributor.authorRozance, P.J.
dc.contributor.authorBrown, L.D.
dc.contributor.authorLorca, R.A.
dc.contributor.authorJulian, C.G.
dc.contributor.authorMoore, L.G.
dc.contributor.authorLimesand, S.W.
dc.contributor.authorWesolowski, S.R.
dc.date.accessioned2021-10-16T02:18:59Z
dc.date.available2021-10-16T02:18:59Z
dc.date.issued2021
dc.identifier.citationJones, A. K., Rozance, P. J., Brown, L. D., Lorca, R. A., Julian, C. G., Moore, L. G., Limesand, S. W., & Wesolowski, S. R. (2021). Uteroplacental nutrient flux and evidence for metabolic reprogramming during sustained hypoxemia. Physiological Reports, 9(18).
dc.identifier.issn2051-817X
dc.identifier.doi10.14814/phy2.15033
dc.identifier.urihttp://hdl.handle.net/10150/662133
dc.description.abstractGestational hypoxemia is often associated with reduced birth weight, yet how hypoxemia controls uteroplacental nutrient metabolism and supply to the fetus is unclear. This study tested the effects of maternal hypoxemia (HOX) between 0.8 and 0.9 gestation on uteroplacental nutrient metabolism and flux to the fetus in pregnant sheep. Despite hypoxemia, uteroplacental and fetal oxygen utilization and net glucose and lactate uptake rates were similar in HOX (n = 11) compared to CON (n = 7) groups. HOX fetuses had increased lactate and pyruvate concentrations and increased net pyruvate output to the utero-placenta. In the HOX group, uteroplacental flux of alanine to the fetus was decreased, as was glutamate flux from the fetus. HOX fetuses had increased alanine and decreased aspartate, serine, and glutamate concentrations. In HOX placental tissue, we identified hypoxic responses that should increase mitochondrial efficiency (decreased SDHB, increased COX4I2) and increase lactate production from pyruvate (increased LDHA protein and LDH activity, decreased LDHB and MPC2), both resembling metabolic reprogramming, but with evidence for decreased (PFK1, PKM2), rather than increased, glycolysis and AMPK phosphorylation. This supports a fetal-uteroplacental shuttle during sustained hypoxemia whereby uteroplacental tissues produce lactate as fuel for the fetus using pyruvate released from the fetus, rather than pyruvate produced from glucose in the placenta, given the absence of increased uteroplacental glucose uptake and glycolytic gene activation. Together, these results provide new mechanisms for how hypoxemia, independent of AMPK activation, regulates uteroplacental metabolism and nutrient allocation to the fetus, which allow the fetus to defend its oxidative metabolism and growth. © 2021 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society.
dc.language.isoen
dc.publisherAmerican Physiological Society
dc.rightsCopyright © 2021 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society. This is an open access article under the terms of the Creative Commons Attribution License.
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectfetal
dc.subjecthypoxemia
dc.subjectmetabolism
dc.subjectuteroplacental
dc.titleUteroplacental nutrient flux and evidence for metabolic reprogramming during sustained hypoxemia
dc.typeArticle
dc.typetext
dc.contributor.departmentSchool of Animal and Comparative Biomedical Sciences, University of Arizona
dc.identifier.journalPhysiological Reports
dc.description.noteOpen access journal
dc.description.collectioninformationThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.
dc.eprint.versionFinal published version
dc.source.journaltitlePhysiological Reports
refterms.dateFOA2021-10-16T02:18:59Z


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Copyright © 2021 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society. This is an open access article under the terms of the Creative Commons Attribution License.
Except where otherwise noted, this item's license is described as Copyright © 2021 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society. This is an open access article under the terms of the Creative Commons Attribution License.