Glyphosate-based herbicide worsens alterations induced by cafeteria diet on rat uterus.
Journal
The Journal of endocrinology
ISSN: 1479-6805
Titre abrégé: J Endocrinol
Pays: England
ID NLM: 0375363
Informations de publication
Date de publication:
01 Apr 2024
01 Apr 2024
Historique:
received:
15
03
2023
accepted:
05
04
2024
medline:
6
4
2024
pubmed:
6
4
2024
entrez:
5
4
2024
Statut:
aheadofprint
Résumé
Exposure to glyphosate-based herbicides (GBH) and consumption of cafeteria (CAF) diet, which are widespread in Western society, seem to be associated with endometrial hyperplasia (EH). Here, we aimed to evaluate the effects of a subchronic low dose of a GBH added to CAF diet on the rat uterus. Female Wistar rats were fed from postnatal day (PND)21 until PND240 with chow (Control) or CAF diet. Since PND140, rats also received GBH (2 mg of glyphosate/kg/day) or water through food, yielding four experimental groups: Control, CAF, GBH and CAF+GBH. On PND240, CAF and CAF+GBH animals showed an increased adiposity index. Respect to Control group, no changes on the serum levels of 17β-estradiol and progesterone were found. However, progesterone levels were higher in CAF+GBH group than in CAF and GBH groups. In the uterus, both studied factors alone and in combination induced morphological and molecular changes associated with EH. Furthermore, the addition of GBH provoked an increased thickness of subepithelial stroma in rats fed with CAF diet. As a consequence of GBH exposure, CAF+GBH rats exhibited an increased density of abnormal gland area, considered preneoplastic lesions, as well as a reduced PTEN and p27 expression, both tumor suppressor molecules that inhibit cell proliferation, respect to Control rats. These results indicate that the addition of GBH exacerbates the CAF-effects on uterine lesions and that the PTEN/p27 signaling pathway seems to be involved. Further studies focusing on the interaction between unhealthy diets and environmental chemicals should be encouraged to better understand uterine pathologies.
Identifiants
pubmed: 38579817
doi: 10.1530/JOE-24-0071
pii: JOE-24-0071
doi:
pii:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM