The DOI matches its Crossref record; 175 of the 177 references it cites were found in a registry or an index.
Placental transport in response to altered maternal nutrition
Open accessAbstract
The mechanisms linking maternal nutrition to fetal growth and programming of adult disease remain to be fully established. We review data on changes in placental transport in response to altered maternal nutrition, including compromized utero-placental blood flow. In human intrauterine growth restriction and in most animal models involving maternal undernutrition or restricted placental blood flow, the activity of placental transporters, in particular for amino acids, is decreased in late pregnancy. The effect of maternal overnutrition on placental transport remains largely unexplored. However, some, but not all, studies in women with diabetes giving birth to large babies indicate an upregulation of placental transporters for amino acids, glucose and fatty acids. These data support the concept that the placenta responds to maternal nutritional cues by altering placental function to match fetal growth to the ability of the maternal supply line to allocate resources to the fetus. On the other hand, some findings in humans and mice suggest that placental transporters are regulated in response to fetal demand signals. These observations are consistent with the idea that fetal signals regulate placental function to compensate for changes in nutrient availability. We propose that the placenta integrates maternal and fetal nutritional cues with information from intrinsic nutrient sensors. Together, these signals regulate placental growth and nutrient transport to balance fetal demand with the ability of the mother to support pregnancy. Thus, the placenta plays a critical role in modulating maternal–fetal resource allocation, thereby affecting fetal growth and the long-term health of the offspring.
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“Thus, the placenta acts as an environmental sensor, integrating signals of the current availability of oxygen and nutrients, maternal stores of nutrient reserves and of the fetal nutrient demands for growth driven by the genes and actual mass of the fetus (74,204).”
From Placental Origins of Chronic Disease (2016) · cites this paper as [204]
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“In addition, maternal nutrition is a major determinant of placental development and alters the morphological, transport and endocrine characteristics of the placenta with consequences for the fetal nutrient supply in a wide range of species including laboratory and farm species as well as human and non-human primates (47, 144, 204, 522, 550).”
From Placental Origins of Chronic Disease (2016) · cites this paper as [204]
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Cites
Repertoires of Autophagy in the Pathogenesis of Ocular Diseases
Li, Y., Jiang, Q. L., Cao, G.-F., Yao, J., & Yan, B. (2015) · Cellular Physiology and Biochemistry · doi:10.1159/000373980 · Cited by 16,351
The Physiology of Reproduction
Legendre, M., & Jalabert, B. (1988) · Annals of Internal Medicine · doi:10.7326/0003-4819-109-2-176_1 · Cited by 7,876
Hyperglycemia and adverse pregnancy outcomes
(2008) · New England Journal of Medicine · doi:10.1056/nejmoa0707943 · Cited by 5,563
mTOR: from growth signal integration to cancer, diabetes and ageing
Zoncu, R., Efeyan, A., & Sabatini, D. M. (2011) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3025 · Cited by 3,941
Effect of In Utero and Early-Life Conditions on Adult Health and Disease
Gluckman, P. D., Hanson, M. A., Cooper, C., & Thornburg, K. L. (2008) · New England Journal of Medicine · doi:10.1056/nejmra0708473 · Cited by 3,898
Onuegbu, A. J., Olisekodiaka, J. M., Udo, J., Umeononihu, O. S., Amah, U. K., Okwara, J. E., & Atuegbu, C. (2015) · Medical Principles and Practice · doi:10.1159/000381778 · Cited by 2,057
Maternal obesity and pregnancy outcome: a study of 287 213 pregnancies in London
Sebire, N. J., Jolly, M., Harris, J. P., Wadsworth, J., Joffe, M., Beard, R. W., Regan, L., & Robinson, S. (2001) · International Journal of Obesity · doi:10.1038/sj.ijo.0801670 · Cited by 1,740
Marshall’s Physiology of Reproduction
Lamming, G. E. (1994) · Springer eBooks · doi:10.1007/978-94-011-1286-4 · Cited by 1,377
Knobil and Neill's Physiology of Reproduction
(2015) · Elsevier eBooks · doi:10.1016/c2011-1-07288-0 · Cited by 1,277
Placental-specific IGF-II is a major modulator of placental and fetal growth
Constância, M., Hemberger, M., Hughes, J., Dean, W., Ferguson-Smith, A., Fundele, R., Stewart, F., Kelsey, G., Fowden, A., Sibley, C., et al. (2002) · Nature · doi:10.1038/nature00819 · Cited by 1,054
Research works printed but not linked: 4
- Gaccioli, 2012, Placental System A and System L amino acid transporter activity and expression in lean and overweight/obese Hispanic women, Reprod Sci, 19, 377A
- Kavitha, 2012, Down regulation of placental amino acid and glucose transporters in response to maternal nutrient restriction in the baboon, Reprod Sci, 19, 378A
- Jansson, 2010, Altered AMPK and mTOR signaling and up-regulation of placental System A amino acid transporter activity and SNAT2 protein expression in obese women giving birth to large babies, Reprod Sci, 17, 260A
- Gaccioli, 2011, Activation of placental mammalian target of rapamycin signaling in obese women, Placenta, 32, A134
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Scott, H. (2021) · Carleton University's Institutional Repository (MacOdrum Library, Carleton University) · doi:10.22215/etd/2021-14714
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Rathor, P., Inani, A., & Vashisth, P. (2023) · Southeast Asian Journal of Health Professional · doi:10.18231/j.sajhp.2023.019
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Skowron, K., Godziszewski, F., Putyrska, A., Łyczkowska, A., Skrzypiec, N., & Orczyk‐Pawiłowicz, M. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27188434
Egong, A. E., Ibe, B. S., Erim, A. E., Onwukwe, T. J., Onwukwe, C. E., & Egbe, N. (2026) · Journal of Radiation Medicine and Biomedical Sciences · doi:10.66353/jrmbs-dgxn2376
Ruggiero, C. H., Radillo, P., Davenport, B. N., Jones, H. N., & Wilson, R. L. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.10.17.759797
Metadata
- Authors
- Gaccioli, F., Lager, S., Powell, T. L., & Jansson, T.
- Affiliations
- The University of Texas at San Antonio Health Science Center (US)
- Corresponding author
- Jansson, T.
- Venue
- Journal of Developmental Origins of Health and Disease
- Publisher
- Cambridge University Press (CUP)
- Published
- 2012-07-31
- Volume
- 4
- Issue
- 2
- Pages
- 101-115
- ISSN
- 2040-1744 (ISSN-L)
- 2040-1752
- PMC
- PMC4237017
- OpenAlex
- W2164709834
- Cited by
- 129
- References
- 177
- Citations by year
- 2026: 13 · 2025: 7 · 2024: 7 · 2023: 12 · 2022: 10 · 2021: 13 · 2020: 11 · 2019: 7 · 2018: 10 · 2017: 15 · 2016: 8 · 2015: 7 · 2014: 4 · 2013: 4 · 2012: 1
- FWCI
- 4.49
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Journal of Developmental Origins of Health and Disease (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (5r01hd068370-11)
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK089989)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (R21HD071306, R01-HD068370, R01HD065007)
- Topics
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Birth, Development, and Health
- Health Sciences › Medicine › Obstetrics and Gynecology › Pregnancy and preeclampsia studies
- Health Sciences › Medicine › Obstetrics and Gynecology › Gestational Diabetes Research and Management
- Keywords
- placental nutrient transport, maternal nutrition, fetal growth restriction, maternal undernutrition, maternal overnutrition, placental blood flow, amino acid transporters, glucose transport, fatty acid uptake, fetal programming, fetal growth, diabetes in pregnancy, placental development
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