Effects of bis (2‐butoxyethyl) phthalate on adrenocortical function in male rats in puberty partially via down‐regulating NR5A1/NR4A1/NR4A2 pathways. Issue 10 (28th June 2022)

• Record Type: Journal Article
• Authors: Liu, Miaoqing; Chen, Haiqiong; Dai, Haipeng; Wang, Yiyan; Li, Jingjing; Tian, Fuhong; Li, Zhongrong; Ge, Ren‐Shan
• Is Part Of: Environmental toxicology. Volume 37:Issue 10(2022)
• Page Start: 2419
• Page End: 2433
• Publication Date: 2022-06-28
• Subjects: adrenal cortex -- bis (2‐butoxyethyl) phthalate -- reactive oxygen species -- steroidogenesis; Water quality bioassay -- Periodicals; Water -- Pollution -- Toxicology -- Periodicals; Microbiological assay -- Periodicals; Toxicity testing -- Periodicals; Environmental toxicology -- Periodicals; Environmental Pollution -- Periodicals; Environmental Pollutants -- Periodicals; Environmental Monitoring -- Periodicals; Écotoxicologie -- Périodiques; Pollution -- Périodiques; 615.902
• DOI: 10.1002/tox.23607
• Languages: English
• ISSNs: 1520-4081

Abstract

Abstract: Phthalates may interfere with the biosynthesis of steroid hormones in the adrenal cortex. Bis (2‐butoxyethyl) phthalate (BBOP) is a phthalate containing oxygen atoms in the alcohol moiety. In this study, 35‐day‐old male Sprague–Dawley rats were daily gavaged with BBOP (0, 10, 100, 250, and 500 mg/kg body weight) for 21 days. BBOP did not affect the weight of body and adrenal glands. BBOP significantly reduced serum corticosterone levels at 250 and 500 mg/kg, and lowered aldosterone level at 500 mg/kg without affecting adrenocorticotropic hormone. BBOP did not alter the thickness of the adrenal cortex. BBOP significantly down‐regulated the expression of steroidogenesis‐related genes ( Scarb1, Star, Cyp11a1, Cyp21, Cyp11b1, Cyp11b2, Nr5a1, Nr4a1, and Nr4a2 ) and proteins, and antioxidant enzymes ( Sod1, Sod2, Gpx1, and Cat ) and their proteins, while up‐regulating the expression of Mc2r and Agtr1a at various doses. BBOP reduced the phosphorylation of AKT1, AKT2, and ERK1/2, as well as the levels of SIRT1 and PGC1α without affecting the phosphorylation of AMPK. BBOP significantly induced the production of reactive oxygen species and apoptosis rate in H295R cells at 100 μM and higher after 24 h of treatment. In conclusion, male rats exposed to BBOP in puberty have significant reduction of steroid biosynthesis with a potential mechanism that is involved in the decrease in the phosphorylation of AKT1, AKT2, ERK1/2, as well as SIRT1 and PGC1α and increase in ROS.