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Impact of intraamniotic inflammation on tryptophan metabolism in the placenta-fetal brain axis in rats

https://doi.org/10.1530/rep-24-0378
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/bdra.23537openalex-snapshot
In utero exposure to venlafaxine, a serotonin–norepinephrine reuptake inhibitor, increases cardiac anomalies and alters placental and heart serotonin signaling in the rat
inferredcites →https://doi.org/10.1002/jnr.24603openalex-snapshot
The placenta‐brain‐axis
inferredcites →https://doi.org/10.1007/s00018-020-03674-wopenalex-snapshot
Regulation of maternal–fetal metabolic communication
inferredcites →https://doi.org/10.1016/0006-8993(88)90703-2openalex-snapshot
Tyrosine availability and brain noradrenaline synthesis in the fetus: control by maternal tyrosine ingestion
inferredcites →https://doi.org/10.1016/j.ajog.2004.06.090openalex-snapshot
Identification of kynurenine pathway enzyme mRNAs and metabolites in human placenta: Up-regulation by inflammatory stimuli and with clinical infection
inferredcites →https://doi.org/10.1016/j.cmet.2023.06.004openalex-snapshot
Tryptophan metabolism in health and disease
inferredcites →https://doi.org/10.1016/j.ebiom.2023.104589openalex-snapshot
CSF neopterin, quinolinic acid and kynurenine/tryptophan ratio are biomarkers of active neuroinflammation
inferredcites →https://doi.org/10.1016/j.ijdevneu.2011.02.011openalex-snapshot
Intrauterine inflammation, insufficient to induce parturition, still evokes fetal and neonatal brain injury
inferredcites →https://doi.org/10.1016/j.it.2022.01.007openalex-snapshot
Maternal inflammation and its ramifications on fetal neurodevelopment
inferredcites →https://doi.org/10.1016/j.jpeds.2011.10.028openalex-snapshot
Placenta-Imprinted Gene Expression Association of Infant Neurobehavior
inferredcites →https://doi.org/10.1016/j.mehy.2013.01.002openalex-snapshot
Placenta-derived hypo-serotonin situations in the developing forebrain cause autism
inferredcites →https://doi.org/10.1016/j.neuroscience.2011.10.005openalex-snapshot
Fetal, maternal, and placental sources of serotonin and new implications for developmental programming of the brain
inferredcites →https://doi.org/10.1016/j.neuroscience.2014.02.021openalex-snapshot
The developmental disruptions of serotonin signaling may involved in autism during early brain development
inferredcites →https://doi.org/10.1016/j.pneurobio.2006.12.003openalex-snapshot
N-Acetylaspartate in the CNS: From neurodiagnostics to neurobiology
inferredcites →https://doi.org/10.1016/j.psyneuen.2019.104371openalex-snapshot
Kynurenine metabolism and inflammation-induced depressed mood: A human experimental study
inferredcites →https://doi.org/10.1016/j.tibs.2023.10.008openalex-snapshot
Why U matters: detection and functions of pseudouridine modifications in mRNAs
inferredcites →https://doi.org/10.1016/s0014-2999(99)00196-xopenalex-snapshot
Tryptophan metabolism and brain function: focus on kynurenine and other indole metabolites
inferredcites →https://doi.org/10.1016/s0143-4004(96)90039-9openalex-snapshot
Functional expression of the plasma membrane serotonin transporter but not the vesicular monoamine transporter in human placental trophoblasts and choriocarcinoma cells
inferredcites →https://doi.org/10.1016/s1472-6483(10)60074-0openalex-snapshot
Expression of placental serotonin transporter and 5-HT 2A receptor in normal and gestational diabetes mellitus pregnancies
inferredcites →https://doi.org/10.1038/jcbfm.2010.156openalex-snapshot
Decreased Cortical Serotonin in Neonatal Rabbits Exposed to Endotoxin in Utero
inferredcites →https://doi.org/10.1038/nature09972openalex-snapshot
A transient placental source of serotonin for the fetal forebrain
inferredcites →https://doi.org/10.1038/s41380-019-0401-9openalex-snapshot
Dysregulation of kynurenine metabolism is related to proinflammatory cytokines, attention, and prefrontal cortex volume in schizophrenia
inferredcites →https://doi.org/10.1038/s41385-022-00495-xopenalex-snapshot
A potent myeloid response is rapidly activated in the lungs of premature Rhesus macaques exposed to intra-uterine inflammation
inferredcites →https://doi.org/10.1042/bsr20150197openalex-snapshot
Tryptophan metabolism, disposition and utilization in pregnancy
inferredcites →https://doi.org/10.1042/ns20220064openalex-snapshot
Maternal immune activation and role of placenta in the prenatal programming of neurodevelopmental disorders
inferredcites →https://doi.org/10.1055/s-0033-1361823openalex-snapshot
Fetal Immune Response to Chorioamnionitis
inferredcites →https://doi.org/10.1067/mob.2001.109653openalex-snapshot
The Preterm Prediction Study: Association between cervical interleukin 6 concentration and spontaneous preterm birth
inferredcites →https://doi.org/10.1073/pnas.0711496105openalex-snapshot
Role of GSK3β in behavioral abnormalities induced by serotonin deficiency
inferredcites →https://doi.org/10.1073/pnas.162212399openalex-snapshot
Global analysis of stress-regulated mRNA turnover by using cDNA arrays
inferredcites →https://doi.org/10.1074/jbc.m113.521161openalex-snapshot
Lipopolysaccharide Activates Toll-like Receptor 4 (TLR4)-mediated NF-κB Signaling Pathway and Proinflammatory Response in Human Pericytes
inferredcites →https://doi.org/10.1080/07853890500472151openalex-snapshot
Asymmetric dimethylarginine (ADMA): A novel risk marker in cardiovascular medicine and beyond
inferredcites →https://doi.org/10.1093/biolre/ioad181openalex-snapshot
Pathological shifts in tryptophan metabolism in human term placenta exposed to LPS or poly I:C
inferredcites →https://doi.org/10.1093/hmg/ddab169openalex-snapshot
Prenatal inflammation as a link between placental expression signature of tryptophan metabolism and preterm birth
inferredcites →https://doi.org/10.1111/aji.12189openalex-snapshot
A Novel Molecular Microbiologic Technique for the Rapid Diagnosis of Microbial Invasion of the Amniotic Cavity and Intra‐Amniotic Infection in Preterm Labor with Intact Membranes
inferredcites →https://doi.org/10.1111/aji.12296openalex-snapshot
Prevalence and Clinical Significance of Sterile Intra-amniotic Inflammation in Patients with Preterm Labor and Intact Membranes
inferredcites →https://doi.org/10.1111/aji.13115openalex-snapshot
Poly(I:C) alters placental and fetal brain amino acid transport in a rat model of maternal immune activation
inferredcites →https://doi.org/10.1111/apha.13478openalex-snapshot
Serotonin homeostasis in the materno‐foetal interface at term: Role of transporters (SERT/SLC6A4 and OCT3/SLC22A3) and monoamine oxidase A (MAO‐A) in uptake and degradation of serotonin by human and rat term placenta
inferredcites →https://doi.org/10.1111/j.1460-9568.2012.08064.xopenalex-snapshot
Pre‐ and postnatal exposure to kynurenine causes cognitive deficits in adulthood
inferredcites →https://doi.org/10.1152/ajplung.00105.2009openalex-snapshot
IL-8 signaling does not mediate intra-amniotic LPS-induced inflammation and maturation in preterm fetal lamb lung
inferredcites →https://doi.org/10.1152/physrev.2000.80.3.1107openalex-snapshot
Creatine and Creatinine Metabolism
inferredcites →https://doi.org/10.1159/000471509openalex-snapshot
Maternal Inflammation Results in Altered Tryptophan Metabolism in Rabbit Placenta and Fetal Brain
inferredcites →https://doi.org/10.1177/1178646917691938openalex-snapshot
Kynurenine Pathway of Tryptophan Metabolism: Regulatory and Functional Aspects
inferredcites →https://doi.org/10.1177/1178646920984163openalex-snapshot
Localization of Indoleamine 2,3-Dioxygenase-1 and Indoleamine 2,3-Dioxygenase-2 at the Human Maternal-Fetal Interface
inferredcites →https://doi.org/10.1177/1753425908100455openalex-snapshot
Intra-amniotic LPS modulation of TLR signaling in lung and blood monocytes of fetal sheep
inferredcites →https://doi.org/10.1177/1933719115604729openalex-snapshot
A Cross-Species Analysis of Animal Models for the Investigation of Preterm Birth Mechanisms
inferredcites →https://doi.org/10.1186/1742-2094-10-87openalex-snapshot
Intracerebroventricular administration of lipopolysaccharide induces indoleamine-2,3-dioxygenase-dependent depression-like behaviors
inferredcites →https://doi.org/10.1186/1743-7075-7-30openalex-snapshot
Role of carnitine in disease
inferredcites →https://doi.org/10.1186/s12958-023-01128-zopenalex-snapshot
Characterization of a human placental clearance system to regulate serotonin levels in the fetoplacental unit
inferredcites →https://doi.org/10.1186/s12974-016-0706-4openalex-snapshot
Intra-amniotic LPS causes acute neuroinflammation in preterm rhesus macaques
inferredcites →https://doi.org/10.1189/jlb.3mr0615-272rropenalex-snapshot
Inflammation and preterm birth
inferredcites →https://doi.org/10.1203/00006450-200001000-00013openalex-snapshot
Cytokine Induction in Fetal Rat Brains and Brain Injury in Neonatal Rats after Maternal Lipopolysaccharide Administration
inferredcites →https://doi.org/10.1203/01.pdr.0000139407.89883.6bopenalex-snapshot
Determining the Fetal Inflammatory Response in an Experimental Model of Intrauterine Inflammation in Rats
inferredcites →https://doi.org/10.1371/journal.pone.0186656openalex-snapshot
Exposure to intrauterine inflammation alters metabolomic profiles in the amniotic fluid, fetal and neonatal brain in the mouse
inferredcites →https://doi.org/10.1503/jpn.240155openalex-snapshot
Elevated plasma B12 and betaine levels in women with anorexia nervosa: possible role in illness pathophysiology and epigenetic regulation
inferredcites →https://doi.org/10.17179/excli2023-6785openalex-snapshot
Metabolomic analysis of the human placenta reveals perturbations in amino acids, purine metabolites, and small organic acids in spontaneous preterm birth
inferredcites →https://doi.org/10.3389/fcell.2020.574034openalex-snapshot
Dynamics of Tryptophan Metabolic Pathways in Human Placenta and Placental-Derived Cells: Effect of Gestation Age and Trophoblast Differentiation
inferredcites →https://doi.org/10.3389/fendo.2022.1061317openalex-snapshot
Serotonin system in the human placenta – the knowns and unknowns
inferredcites →https://doi.org/10.3389/fimmu.2024.1416162openalex-snapshot
IL-1 and TNF mediates IL-6 signaling at the maternal-fetal interface during intrauterine inflammation
inferredcites →https://doi.org/10.3389/fnagi.2022.893159openalex-snapshot
Coenzyme A-Dependent Tricarboxylic Acid Cycle Enzymes Are Decreased in Alzheimer’s Disease Consistent With Cerebral Pantothenate Deficiency
inferredcites →https://doi.org/10.3389/fphar.2022.871193openalex-snapshot
Development of a Rat Model of Intra-Amniotic Inflammation via Ultrasound-Guided Administration of a Triggering Agent in the Gestational Sac to Enable Analysis of Individual Amniotic Fluid Samples
inferredcites →https://doi.org/10.3390/ijms18071595openalex-snapshot
Redox Properties of Tryptophan Metabolism and the Concept of Tryptophan Use in Pregnancy
inferredcites →https://doi.org/10.3390/ijms21207578openalex-snapshot
Profiling of Tryptophan Metabolic Pathways in the Rat Fetoplacental Unit during Gestation
inferredcites →https://doi.org/10.3390/ijms25020853openalex-snapshot
The Influence of Kynurenine Metabolites on Neurodegenerative Pathologies
inferredcites →https://doi.org/10.3402/tdp.v1i0.20593openalex-snapshot
Placental tryptophan metabolism as a potential novel pathway for the developmental origins of mental diseases
inferredcites →https://doi.org/10.4161/epi.25358openalex-snapshot
PlacentalHTR2Amethylation is associated with infant neurobehavioral outcomes

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← backgroundhttps://doi.org/10.5281/zenodo.16419449zenodo-depositor-declared
inferred← citeshttps://doi.org/10.1093/humupd/dmag001openalex-snapshot
The placental tryptophan pathway across gestation: implications for pregnancy outcomes
inferred← citeshttps://doi.org/10.3390/nu18152575openalex-snapshot
Diminished Maternal Tryptophan Leads to Sexually Dimorphic Differences in the Placenta–Brain Axis
inferred← citeshttps://doi.org/10.64898/2026.06.24.734303openalex-snapshot
Fragmented sleep during pregnancy induces inflammation and tryptophan-kynurenine pathway metabolism: Importance of elevated fetal brain kynurenic acid
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