» Articles » PMID: 37021957

Chronic Exposure to a Mixture of Phthalates Shifts the White and Brown Adipose Tissue Phenotypes in Female Mice

Overview
Journal Toxicol Sci
Specialty Toxicology
Date 2023 Apr 6
PMID 37021957
Authors
Affiliations
Soon will be listed here.
Abstract

Phthalates are endocrine-disrupting chemicals used in consumer products. Although phthalates are obesogens and affect metabolic function, it is unknown if chronic exposure for 6 months to a phthalate mixture alters adipose tissue phenotype in female mice. After vehicle or mixture exposure, white adipose tissue and brown adipose tissue (WAT and BAT) were analyzed for expression of adipogenesis, proliferation, angiogenesis, apoptosis, oxidative stress, inflammation, and collagen deposition markers. The mixture altered WAT morphology, leading to an increase in hyperplasia, blood vessel number, and expression of BAT markers (Adipoq and Fgf2) in WAT. The mixture increased the expression of the inflammatory markers, Il1β, Ccl2, and Ccl5, in WAT. The mixture also increased expression of the proapoptotic (Bax and Bcl2) and antiapoptotic (Bcl2l10) factors in WAT. The mixture increased expression of the antioxidant Gpx1 in WAT. The mixture changed BAT morphology by increasing adipocyte diameter, whitening area, and blood vessel number and decreased expression of the thermogenic markers Ucp1, Pgargc1a, and Adrb3. Furthermore, the mixture increased the expression of adipogenic markers Plin1 and Cebpa, increased mast cell number, and increased Il1β expression in BAT. The mixture also increased expression of the antioxidant markers Gpx and Nrf2 and the apoptotic marker Casp2 in BAT. Collectively, these data indicate that chronic exposure to a phthalate mixture alters WAT and BAT lipid metabolism phenotypes in female mice, leading to an apparent shift in their normal morphology. Following long-term exposure to a phthalate mixture, WAT presented BAT-like features and BAT presented WAT-like features.

Citing Articles

Serum Phthalate Concentrations and Biomarkers of Oxidative Stress in Adipose Tissue in a Spanish Adult Cohort.

Perez-Diaz C, Perez-Carrascosa F, Riquelme-Gallego B, Villegas-Arana E, Armendariz A, Galindo-Angel J Environ Sci Technol. 2024; 58(18):7719-7730.

PMID: 38651840 PMC: 11080070. DOI: 10.1021/acs.est.3c07150.

References
1.
Chouchani E, Kazak L, Spiegelman B . New Advances in Adaptive Thermogenesis: UCP1 and Beyond. Cell Metab. 2018; 29(1):27-37. DOI: 10.1016/j.cmet.2018.11.002. View

2.
Koch H, Calafat A . Human body burdens of chemicals used in plastic manufacture. Philos Trans R Soc Lond B Biol Sci. 2009; 364(1526):2063-78. PMC: 2873011. DOI: 10.1098/rstb.2008.0208. View

3.
Ricquier D, Bouillaud F . Mitochondrial uncoupling proteins: from mitochondria to the regulation of energy balance. J Physiol. 2000; 529 Pt 1:3-10. PMC: 2270181. DOI: 10.1111/j.1469-7793.2000.00003.x. View

4.
Ozben T . Oxidative stress and apoptosis: impact on cancer therapy. J Pharm Sci. 2007; 96(9):2181-96. DOI: 10.1002/jps.20874. View

5.
Brehm E, Flaws J . Prenatal exposure to a mixture of phthalates accelerates the age-related decline in reproductive capacity but may not affect direct biomarkers of ovarian aging in the F1 generation of female mice. Environ Epigenet. 2021; 7(1):dvab010. PMC: 8543146. DOI: 10.1093/eep/dvab010. View