Pre-Conceptional Exposure to Glyphosate Affects the Maternal Hepatic and Ovarian Proteome.
Animals
Female
Mice
Pregnancy
Chromatography, Liquid
Endoplasmic Reticulum
Golgi Apparatus
Maternal Exposure
/ adverse effects
Mice, Inbred C57BL
Prenatal Exposure Delayed Effects
Proteome
Tandem Mass Spectrometry
Vesicular Transport Proteins
Herbicides
/ toxicity
Liver
Ovary
/ metabolism
Glyphosate
glyphosate
ovary
pregnancy
proteome
Journal
Toxicological sciences : an official journal of the Society of Toxicology
ISSN: 1096-0929
Titre abrégé: Toxicol Sci
Pays: United States
ID NLM: 9805461
Informations de publication
Date de publication:
23 11 2022
23 11 2022
Historique:
pubmed:
30
9
2022
medline:
30
11
2022
entrez:
29
9
2022
Statut:
ppublish
Résumé
Exposure to glyphosate (GLY), a commonly used herbicide, is supported by urinary detection and associated with shortened gestation in women. This study tested the hypothesis that chronic low-dose pre-conceptional GLY exposure would affect maternal ovarian function mid- and post-gestation. Mice (C57BL/6; n = 40) were exposed per os to saline vehicle control (CT; n = 20) or GLY (2 mg/kg; n = 20) daily for 10 weeks starting at 7 weeks of age. Post-exposure, females were impregnated and euthanized at gestation day 14 (GD14) or post-weaning (PW). Pregnancy success was reduced from 75% to 55% by GLY exposure. No treatment effect (p > .05) on body weight, maternal serum 17β-estradiol, or litter size was noted. Ovarian weight was unaffected or reduced (p < .05) by GLY in GD14 and PW dams, respectively. Exposure to GLY decreased (p < .05) PW ovarian secondary follicle number with no other follicle composition impacts. Protein abundance analysis by LC-MS/MS identified that GLY altered (p < .05) 26 ovarian and 41 hepatic proteins in GD14 dams and 39 hepatic proteins in PW dams. In GD14 dams, GLY increased ovarian protein abundance of SEC16A (p < .05; 29-fold) and hepatic RPS27L and GM4952 (p < .05; ∼4-fold). In both GD14 and PW dams, GLY exposure increased (p < .05) hepatic RPS4 and decreased (p < .05) ECHDC3. Pathway analysis using DAVID identified 10 GLY hepatic pathway targets with FDR ≤ 0.07 in GD14 dams.
Identifiants
pubmed: 36173347
pii: 6730775
doi: 10.1093/toxsci/kfac098
pmc: PMC9702999
doi:
Substances chimiques
Proteome
0
Vesicular Transport Proteins
0
Herbicides
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
204-214Subventions
Organisme : NIEHS NIH HHS
ID : R21 ES026282
Pays : United States
Informations de copyright
© The Author(s) 2022. Published by Oxford University Press on behalf of the Society of Toxicology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.
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