PUBLICATION

Anti-estrogenic effect of semicarbazide in female zebrafish (Danio rerio) and its potential mechanisms

Authors
Yu, M., Zhang, X., Guo, L., Tian, H., Wang, W., Ru, S.
ID
ZDB-PUB-151222-6
Date
2016
Source
Aquatic toxicology (Amsterdam, Netherlands)   170: 262-270 (Journal)
Registered Authors
Keywords
17β-Estradiol, Gamma-aminobutyric acid, Leptin, Semicarbazide, Steroidogenic genes, Zebrafish
MeSH Terms
  • Animals
  • Brain/drug effects
  • Brain/metabolism
  • Estrogen Receptor Modulators/toxicity*
  • Female
  • Gonadal Steroid Hormones/blood
  • Ovary/drug effects
  • Ovary/metabolism
  • Ovary/pathology
  • RNA, Messenger/genetics
  • RNA, Messenger/metabolism
  • Semicarbazides/toxicity*
  • Transcription, Genetic/drug effects
  • Vitellogenins/metabolism
  • Zebrafish/blood
  • Zebrafish/genetics
  • Zebrafish/metabolism*
PubMed
26688189 Full text @ Aquat. Toxicol.
Abstract
Semicarbazide (SMC), a member of the hydrazine family, has various toxic effects and has been detected in organisms, aquatic environments, and food. SMC exposure inhibited the transcription of hepatic vitellogenin and estrogen receptors in female zebrafish (Danio rerio), suggesting that it had anti-estrogenic properties. In order to elucidate the mechanisms underlying these, we exposed female zebrafish to SMC and used enzyme-linked immunosorbent assays to examine plasma 17β-estradiol (E2) and testosterone (T) levels. Gonad histology was analyzed and the mRNA expression of genes involved in the reproductive axis, the gamma-aminobutyric acid (GABA) shunt, and leptin was quantified by real-time PCR. Zebrafish were exposed to 1, 10, 100, or 1000μg/L SMC in a semi-static system for 96hours or 28 days. Plasma E2 levels were significantly decreased and ovarian maturation was inhibited by SMC, suggesting that its anti-estrogenic effect was exerted by reducing endogenous E2 levels. This was likely due to the SMC-mediated inhibition of cytochrome P450 (CYP) 19A mRNA levels, because this enzyme catalyzes the conversion of T to E2 in the gonads. In addition, down-regulation of the mRNA expression of 3-hydroxy-3-methylglutaryl coenzyme A reductase, steroidogenic acute regulatory protein, CYP17, and 17beta-hydroxysteroid dehydrogenase was observed; this was predicted to reduce T concentrations and further contribute to the reduced E2 levels. SMC-induced changes in the expression of these steroidogenic genes correlated with decreased transcription of gonadotropic hormones (follicle-stimulating hormone and luteinizing hormone) and significantly elevated leptin expression. Furthermore, SMC also altered expression of the key enzyme in gamma-aminobutyric acid (GABA) synthesis, GABA receptors, and salmon gonadotropin-releasing hormone, thus affecting gonadotropin expression. Overall, SMC acted at multiple sites related to reproduction to reduce plasma E2 levels, consequently exerting an anti-estrogenic effect in female zebrafish. These effects were observed at environmentally relevant concentrations and highlight the importance of controlling SMC contamination.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping