Inhibition of human and rat placental 3β-hydroxysteroid dehydrogenase/Δ5, 4-isomerase activities by insecticides and fungicides: Mode action by docking analysis. (5th January 2023)

• Record Type: Journal Article
• Authors: Li, Jingjing; Tian, Fuhong; Tang, Yunbing; Shi, Lei; Wang, Shaowei; Hu, Zhiyan; Zhu, Yang; Wang, Yiyan; Li, Huitao; Ge, Ren-shan; Li, Xiaoheng
• Is Part Of: Chemico-biological interactions. Volume 369(2023)
• Publication Date: 2023-01-05
• Subjects: 3β-Hydroxysteroid dehydrogenase/Δ5, 4-isomerase -- Pregnenolone -- Progesterone -- Steroidogenesis -- Placenta -- Inhibitors; Biochemistry -- Periodicals; Toxicological chemistry -- Periodicals; Biochemistry -- Periodicals; Biologie moléculaire -- Périodiques; Biochimie -- Périodiques; Toxicologie biochimique -- Périodiques; 572
• DOI: 10.1016/j.cbi.2022.110292
• Languages: English
• ISSNs: 0009-2797

Abstract

Abstract: Many insecticides and fungicides are endocrine-disrupting compounds, which possibly interfere with the placental endocrine system. In the placenta, 3β-hydroxysteroid dehydrogenase/Δ 5, 4 -isomerase type 1 (HSD3B1) is the major steroidogenic enzyme, which makes progesterone from pregnenolone to support the placental stability. In this study, we screened 12 classes of insecticides and fungicides to inhibit placental HSD3B1 activity and compared them to the rat homolog type 4 (HSD3B4) isoform. Human HSD3B1 activity and rat HSD3B4 activity were measured in the presence of 200 nM pregnenolone and 0.2 mM NAD + and 100 μM of test chemical. Triclosan, triflumizole, dichlone, and oxine at 100 μM significantly inhibited human HSD3B1 activity with the residual activity being less than 50% of the control. Further study showed that the half-maximal inhibitory concentration (IC50 ) values of triclosan, triflumizole, dichlone, and oxine were 85.53 ± 9.14, 73.75 ± 3.42, 2.54 ± 0.40, and 102.93 ± 6.10 μM, respectively. In the presence of pregnenolone, triclosan, triflumizole, and dichlone were mixed inhibitors of HSD3B1, while oxine was a noncompetitive inhibitor. In the presence of NAD +, triclosan exhibited competitive inhibition while triflumizole possessed uncompetitive inhibition. Docking analysis showed that triclosan bound NAD + -binding site, while triflumizole, dichlone, and oxine mostly bound steroid-binding site. When the effect of these insecticides on rat placental HSD3B4 activity was screened in the presence of 200 nM pregnenolone, atrazine, triclosan, triflumizole, oxine, cyprodinil, and diphenyltin at 100 μM significantly inhibited rat HSD3B4 activity, with IC50 values of triclosan, triflumizole, oxine, and cyprodinil were 82.99 ± 6.48, 35.45 ± 2.73, 105.59 ± 12.04, and 43.37 ± 3.00 μM, respectively. The mode action analysis showed that t riflumizole and cyprodinil were almost competitive inhibitors, while triclosan and oxine were almost noncompetitive inhibitors of rat HSD3B4. Docking analysis showed that triclosan and oxine bound cofactor NAD + binding residues more than steroid-binding residues of rat HSD3B4 while triflumizole and cyprodinil bound most pregnenolone-interactive residues. In conclusion, some insecticides such as triclosan, triflumizole, and oxine can effectively inhibit both human and rat placental HSD3B activity and they have unique mode action due to the structure difference. Graphical abstract: Image 1 Highlights: Triclosan, triflumizole, and dichlone are mixed inhibitors of human HSD3B1. Triclosan, triflumizole, cyprodinil are mixed inhibitors of rat HSD3B4. Oxine is a non-competitive inhibitor of human HSD3B1 and rat HSD3B4. Primary structure difference in catalytic residue S125T may explain the species-dependent difference of these chemicals.