TY - JOUR
T1 - Sexually dimorphic effects of in-utero exposure to a real-life environmental chemical mixture on markers of cardiovascular function in adult sheep
AU - Khan, Noor Muhammad
AU - Vyas, Arpita
AU - Ghasemzadeh-Hasankolaei, Mohammad
AU - Padmanabhan, Vasantha
AU - Evans, Neil P.
AU - Bellingham, Michelle
N1 - Publisher Copyright:
© 2025 The Authors
PY - 2025/12
Y1 - 2025/12
N2 - Cardiovascular disease (CVD) is a major sexually dimorphic cause of mortality and morbidity. Prenatal exposure to environmental chemicals (ECs) can program the adult onset of CVD. Using a real-life EC exposure sheep model, this study investigated structural and molecular underpinnings of the sex-specific effects of prenatal EC mixture exposure via mothers grazing on biosolids treated pasture (BTP) in left ventricular (LV) tissues. EC mixture exposure had no impact on plasma TG and TC levels, LV cardiomyocyte number or collagen scoring in both sexes. However, a significant increase (P < 0.05) in fibrosis was evident in interstitial, perivascular and replacement fibrosis in BTP males. A significant upregulation of inflammatory (MHC-DRB1, MHC-DYA), apoptosis (CASP3) markers, together with elevated IGF-1 and IGF1-R expression was restricted to EC exposed males only. These findings extend our earlier results on sex-specific differences in prenatal EC exposure programming of adult CV functioning, particularly in males.
AB - Cardiovascular disease (CVD) is a major sexually dimorphic cause of mortality and morbidity. Prenatal exposure to environmental chemicals (ECs) can program the adult onset of CVD. Using a real-life EC exposure sheep model, this study investigated structural and molecular underpinnings of the sex-specific effects of prenatal EC mixture exposure via mothers grazing on biosolids treated pasture (BTP) in left ventricular (LV) tissues. EC mixture exposure had no impact on plasma TG and TC levels, LV cardiomyocyte number or collagen scoring in both sexes. However, a significant increase (P < 0.05) in fibrosis was evident in interstitial, perivascular and replacement fibrosis in BTP males. A significant upregulation of inflammatory (MHC-DRB1, MHC-DYA), apoptosis (CASP3) markers, together with elevated IGF-1 and IGF1-R expression was restricted to EC exposed males only. These findings extend our earlier results on sex-specific differences in prenatal EC exposure programming of adult CV functioning, particularly in males.
KW - Cardiovascular diseases
KW - CASP3
KW - Environmental Chemicals
KW - IGF-1
KW - IGF1-R
KW - Sheep
UR - https://www.scopus.com/pages/publications/105022245461
U2 - 10.1016/j.etap.2025.104869
DO - 10.1016/j.etap.2025.104869
M3 - Article
C2 - 41242581
AN - SCOPUS:105022245461
SN - 1382-6689
VL - 120
JO - Environmental Toxicology and Pharmacology
JF - Environmental Toxicology and Pharmacology
M1 - 104869
ER -