Paternal cadmium exposure affects estradiol synthesis by impairing intracellular cholesterol homeostasis and mitochondrial function in offspring female mice

Yanwei Zhang; Jinzhao Zhou; Ling Zeng; Yifan Xiong; Xiaofei Wang; Wenpei Xiang; Ping Su

doi:10.1016/j.ecoenv.2023.115280

Paternal cadmium exposure affects estradiol synthesis by impairing intracellular cholesterol homeostasis and mitochondrial function in offspring female mice

Ecotoxicol Environ Saf. 2023 Sep 15:263:115280. doi: 10.1016/j.ecoenv.2023.115280. Epub 2023 Jul 21.

Authors

Yanwei Zhang¹, Jinzhao Zhou¹, Ling Zeng², Yifan Xiong³, Xiaofei Wang¹, Wenpei Xiang⁴, Ping Su⁵

Affiliations

¹ Institute of Reproductive Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
² Medical Genetics Center, Maternal and Child Health Hospital of Hubei Province, Wuhan, China.
³ Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
⁴ Institute of Reproductive Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China; Wuhan Huake Reproductive Hospital, Wuhan, Hubei 430013, China.
⁵ Institute of Reproductive Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China; Wuhan Huake Reproductive Hospital, Wuhan, Hubei 430013, China. Electronic address: suping24@mails.tjmu.edu.cn.

PMID: 37481860
DOI: 10.1016/j.ecoenv.2023.115280

Abstract

Cadmium (Cd) is a toxic heavy metal commonly found in nature and an endocrine disrupting chemical (EDC). Previous studies found that Cd can damage several organs, including the kidneys, bones, cardiovascular system and reproductive system. However, the effect of paternal Cd exposure on the offspring is unclear. In this study, 1 mg/kg of cadmium chloride (CdCl₂) was injected intraperitoneally every other day in 8-week-old C57BL/6 J male mice to study the effects on their female offspring. Our results showed an increase in body weight, water intake and food intake in F1 female mice from the Cd-exposed group. The development of secondary follicles and antral follicles in the ovaries of Cd-treated was inhibited. Serum estradiol (E2) was found to be decreased. Further analysis revealed significant downregulation of StAR, P450scc, 17β-HSD, CYP17A1 and CYP19A1, which are related to E2 synthesis. Serum total cholesterol was increased and free cholesterol was reduced. Total cholesterol in ovarian tissue was decreased. qRT-PCR and Western blot analysis revealed a decrease in the mRNA and protein expression of HMGCR, LDLR, and ABCA1, which are associated with cholesterol homeostasis. Oil red O staining indicated that lipid droplets (LDs) were accumulated in ovarian tissues, while the expression of ATGL and HSL proteins associated with lipid droplet degradation was significantly downregulated. In juvenile female mice, ultrastructural alterations of mitochondria in the ovaries were observed by transmission electron microscopy (TEM). In adult female mice, the expression of proteins associated with mitochondrial dynamics (DRP1 and MFN2) was significantly reduced in the ovaries. Overall, our study suggests that paternal Cd exposure inhibits follicular development, and affects serum E2 synthesis by impairing cholesterol homeostasis and affecting mitochondrial function.

Keywords: Cadmium; Cholesterol; Estradiol; Intergenerational inheritance; Mitochondrial dynamics.

MeSH terms

Animals
Cadmium* / toxicity
Cholesterol
Estradiol*
Female
Homeostasis
Male
Mice
Mice, Inbred C57BL
Mitochondria / metabolism

Substances

Cadmium
Estradiol
Cholesterol