Estrogenic activity of zinc pyrithione: an in vivo and in vitro study
- Author:
Kyung Sik YOON
1
;
Namhee YOUN
;
Hyungyung GU
;
Seung Jun KWACK
Author Information
- Publication Type:Original Article
- Keywords: Zinc pyrithione; Estrogenic activity; Uterotrophic assay; E-screen assay; Gene expression analysis
- MeSH: Animals; Breast Neoplasms; Cell Proliferation; Cell Survival; Dandruff; Dermatitis, Seborrheic; Estrogens; Gene Expression; Gene Expression Profiling; In Vitro Techniques; MCF-7 Cells; Rats; Uterus; Weights and Measures; Zinc
- From:Environmental Health and Toxicology 2017;32(1):2017004-
- CountryRepublic of Korea
- Language:English
- Abstract: Zinc pyrithione (ZP) is commonly used to prevent dandruff and seborrheic dermatitis. Many consumers are exposed daily to high doses of ZP, causing serious concerns about its toxicity. The reproductive and developmental toxicities were previously reported in pregnant rats. However, the estrogenic activity of ZP at varying degrees of exposure has been rarely studied. Thus, we performed an uterotrophic assay, E-screen assay, and gene expression profiling to assess the estrogenic activity of ZP. For the uterotrophic assay, ZP (2, 10, or 50 mg/kg/d) was subcutaneously administered to ovariectomized rats every day for three days. Uteri were extracted 24 hours after the last dose. Then, wet and blotted uterine weights were measured. For the E-screen essay, MCF-7 cells (a breast cancer cell line) were exposed to 10⁻⁹ to 10⁻⁶ M of ZP, and cell proliferation was then measured. For the gene expression analysis, changes of gene expression levels in uterine samples taken for the uterotrophic assay were analyzed. In the uterotrophic assay, the concentration of ZP had no significant effect on uterine weight. In the E-screen assay, ZP at any concentration showed no significant increase in MCF-7 cell proliferation, compared to the control group. However, 10⁻⁶ M of ZP significantly reduced cell viability. The changes in gene expression slightly differed between the ZP and control groups. The in vivo and in vitro assays, together with gene expression analysis, demonstrated that ZP showed no significant estrogenic activity.
