Metabolomics, Journal Year: 2023, Volume and Issue: unknown, P. 307 - 362
Published: Jan. 1, 2023
Language: Английский
Metabolomics, Journal Year: 2023, Volume and Issue: unknown, P. 307 - 362
Published: Jan. 1, 2023
Language: Английский
Environmental Science and Pollution Research, Journal Year: 2023, Volume and Issue: 30(34), P. 81450 - 81473
Published: Jan. 13, 2023
Language: Английский
Citations
39Environmental Pollution, Journal Year: 2023, Volume and Issue: 320, P. 121071 - 121071
Published: Jan. 13, 2023
Language: Английский
Citations
31Metabolites, Journal Year: 2021, Volume and Issue: 11(8), P. 485 - 485
Published: July 27, 2021
Environmental pollution causes significant toxicity to ecosystems. Thus, acquiring a deeper understanding of the concentration environmental pollutants in ecosystems and, clarifying their potential toxicities is great significance. metabolomics powerful technique investigating effects on living organisms environment. In this review, we cover different aspects approach, which allows acquisition reliable data. A step-by-step procedure from sample preparation data interpretation also discussed. Additionally, other factors, including model and various types emerging toxicants are Moreover, considerations for successful as well identification toxic based combination with phenotype assays. Finally, induced by application
Language: Английский
Citations
28Environment International, Journal Year: 2022, Volume and Issue: 169, P. 107530 - 107530
Published: Sept. 17, 2022
Human and animal exposure to bisphenol A (BPA) has been associated with adverse developmental reproductive effects. The molecular mechanisms by which BPA exerts its effects are not well-understood, even less known about analogues F (BPF). To address these knowledge gaps, we conducted an untargeted metabolome-wide association study (MWAS) identify metabolic perturbations BPA/BPF exposures in a pregnant African American cohort.From subset of participants enrolled the Atlanta Maternal-Child cohort, collected both urine samples, for targeted assessment (N = 230) BPF 48), serum high-resolution metabolomics (HRM) profiling 230), during early pregnancy (8-14 weeks' gestation). Using established HRM workflow consisting MWAS modeling, pathway enrichment analysis, chemical annotation confirmation, investigated potential pathways features exposures.The geometric mean creatinine-adjusted concentrations urinary were 0.85 ± 2.58 0.70 4.71 µg/g creatinine, respectively. After false positive discovery rate correction at 20 % level, 264 733 unique significantly concentrations, representing 10 12 pathways, Three including steroid hormones biosynthesis, lysine lipoate metabolism, exposure. standards, have confirmed identity 16 metabolites or exposure.Our findings support that women is perturbation aromatic amino acid xenobiotics other metabolism closely linked stress responses, inflammation, neural development, reproduction, weight regulation.
Language: Английский
Citations
22Chemosphere, Journal Year: 2023, Volume and Issue: 317, P. 137830 - 137830
Published: Jan. 11, 2023
Language: Английский
Citations
12Metabolomics, Journal Year: 2025, Volume and Issue: 21(1)
Published: Jan. 25, 2025
Abstract Background Gestational exposure to non-persistent endocrine-disrupting chemicals (EDCs) may be associated with adverse pregnancy outcomes. While many EDCs affect the endocrine system, their effects on endocrine-related metabolic pathways remain unclear. This study aims explore global metabolome changes EDC biomarkers at delivery. Methods included 75 pregnant individuals who delivered University of Cincinnati Hospital from 2014 2017. We measured maternal urinary paraben/phenol (12), phthalate (13), and replacements (4) samples collected during delivery visit. Global serum profiles were analyzed blood ( n = 72) newborn 63) cord Fifteen 29 excluded due low detection frequency or potential exposures hospital stay. assessed metabolome-wide associations between 14 maternal/newborn profiles. Additionally, performed enrichment analysis identify alterations in pathways. Results observed concentrations metabolites (mono-isobutyl phthalate), (mono-2-ethyl-5-carboxypentyl terephthalate, mono-2-ethyl-5-hydroxyhexyl terephthalate) phenols (bisphenol-A, bisphenol-S) metabolome, using q-value < 0.2 as a threshold. (mono-n-butyl phthalate, monobenzyl phthalate) (2,5-dichlorophenol, BPA) noted. Enrichment analyses revealed (p-gamma 0.05) amino acid, carbohydrate, lipid, glycan, vitamin, other cofactor metabolism Conclusion Maternal paraben, phenol, replacement biomarker metabolome.
Language: Английский
Citations
0Journal of Hazardous Materials, Journal Year: 2023, Volume and Issue: 459, P. 132155 - 132155
Published: July 26, 2023
Language: Английский
Citations
8The Science of The Total Environment, Journal Year: 2024, Volume and Issue: 948, P. 174922 - 174922
Published: July 20, 2024
Language: Английский
Citations
3Metabolites, Journal Year: 2021, Volume and Issue: 11(10), P. 666 - 666
Published: Sept. 29, 2021
Bisphenols are used in the production of polycarbonate plastics and epoxy resins. Bisphenol A (BPA) has been widely studied is believed to act as an endocrine disruptor. F (BPF) bisphenol S (BPS) have increasingly employed replacements for BPA, although previous studies suggested that they yield similar physiological responses several organisms. Daphnia magna a common model organism ecotoxicology was exposed sub-lethal concentrations BPF, BPS investigate disruption metabolic profiles. Targeted metabolite analysis by liquid chromatography-tandem mass spectrometry (LC-MS/MS) measure polar metabolites extracted from D. magna, which linked range biochemical pathways. Multivariate analyses individual changes showed non-monotonic concentration all three bisphenols (BPA, BPS). Pathway indicated perturbation distinct pathways, mostly associated with protein synthesis, amino acid metabolism, energy metabolism. Overall, we observed can be chemical class (bisphenols) well related each type (A, F, S). These findings further demonstrate need using metabolomic exposure assessment, especially chemicals within same may disrupt biochemistry uniquely at molecular-level.
Language: Английский
Citations
14Biomedicines, Journal Year: 2024, Volume and Issue: 12(12), P. 2678 - 2678
Published: Nov. 25, 2024
Background: Autism spectrum disorders (ASDs), attention-deficit disorder (ADHD), Parkinson’s disease (PD), polycystic ovary (PCOS), and Alzheimer’s (AD) have all been linked to exposure bisphenol A (BPA). Methods: This paper is a review discussion of the published literature. Results: Animal studies shown BPA be broad-spectrum endocrine disruptor. metabolized via glucuronidation pathway, which involves addition glucose target molecule, catalyzed by uridine 5′-diphospho-glucuronosyltransferases (UGTs). Evidence compromised has found for ASD, DHD, PD, PCOS. Genetic polymorphisms that alter catalytic activity UGTs efflux transporters involved are common. There two ways interpret findings associations between efficiency disease, ‘direct’ pathway an ‘indirect’ pathway. With free actual causative agent. Compromised detoxification leads higher concentrations in vulnerable tissues. Decreased increased tissues BPA, where it can function as not serves marker decreased another unknown compound endogenous origin detoxified similar combination BPA. It this compound(s), acting disruptor, metabolic environment favors development over extended time period. Conclusion: existing literature supports indirect ‘marker’ hypothesis hypothesis.
Language: Английский
Citations
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