Přehled o publikaci
2025
2-Ethylhexyl Diphenyl Phosphate Affects Steroidogenesis and Lipidome Profile in Human Adrenal (H295R) Cells
NEGI, Chander Kant; Darshak Chandulal GADARA; Lola Murielle BAJARD ÉP.ESNER; Zdeněk SPÁČIL; Luděk BLÁHA et. al.Základní údaje
Originální název
2-Ethylhexyl Diphenyl Phosphate Affects Steroidogenesis and Lipidome Profile in Human Adrenal (H295R) Cells
Autoři
NEGI, Chander Kant; Darshak Chandulal GADARA; Lola Murielle BAJARD ÉP.ESNER; Zdeněk SPÁČIL a Luděk BLÁHA
Vydání
CHEMICAL RESEARCH IN TOXICOLOGY, WASHINGTON, AMER CHEMICAL SOC, 2025, 0893-228X
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Organizace
Přírodovědecká fakulta – Masarykova univerzita – Repozitář
UT WoS
001458664800001
EID Scopus
2-s2.0-105001986461
Klíčová slova anglicky
ORGANOPHOSPHORUS FLAME RETARDANTS; GENE-EXPRESSION; CHOLESTEROL; METABOLISM; CHEMICALS
Návaznosti
LM2023069, projekt VaV. 857560, interní kód Repo. 859891, interní kód Repo.
Změněno: 16. 7. 2025 00:50, RNDr. Daniel Jakubík
Anotace
V originále
The ever-increasing use of chemicals and the rising incidence of adverse reproductive effects in the modern environment have become an emerging concern. Several studies have shown that environmental contaminants, such as organophosphate flame retardants (OPFRs), negatively impact reproductive health. To evaluate the potential endocrine-related adverse reproductive effects of widely used and priority-listed compound 2-Ethylhexyl diphenyl phosphate (EHDPP), we characterized its effects on adrenal steroidogenesis in human adrenocortical (H295R) cells. The cells were exposed to EHDPP (1 and 5 mu M) for 48 h, and the production of hormones, including progesterone, androstenedione, testosterone, estradiol, cortisol, and aldosterone, was measured. In addition, LC-MS/MS-based lipidomics analysis was done to quantify intracellular lipid profiles, and transcriptional assays were performed to examine the expression of genes related to corticosteroidogenesis, lipid metabolism, and mitochondrial dynamics. Our findings indicate that EHDPP disrupts hormone regulation in vitro, as evidenced by increased estradiol, cortisol, and aldosterone secretion. The expression of key corticosteroidogenic genes (CYP11B2, CYP21A1, 3 beta-HSD2, and 17 beta-HSD1) was upregulated significantly upon EHDPP exposure. Intracellular lipidomics revealed EHDPP-mediated disruption, including reduced total cholesterol ester, sphingolipids, and increased phospholipids, triglyceride species, and saturated-monounsaturated lipids subspecies. These alterations were accompanied by decreased ACAT2 and SCD1 gene expression. Moreover, a shift in mitochondrial dynamics was indicated by increased MF1 expression and decreased FIS1 expression. These data suggest that EHDPP disrupts adrenal steroidogenesis and lipid homeostasis, emphasizing its potential endocrine-disrupting effects.