Acute 7,12-dimethylbenz[a]anthracene exposure causes differential concentration-dependent follicle depletion and gene expression in neonatal rat ovaries

Jill A. Madden, Patricia B Hoyer, Patrick J. Devine, Aileen F. Keating

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

Chronic exposure to the polycyclic aromatic hydrocarbon 7,12-dimethylbenz[a]anthracene (DMBA), generated during combustion of organic matter including cigarette smoke, depletes all ovarian follicle types in the mouse and rat, and in vitro models mimic this effect. To investigate the mechanisms involved in follicular depletion during acute DMBA exposure, two concentrations of DMBA at which follicle depletion has (75nM) and has not (12.5nM) been observed were investigated. Postnatal day four F344 rat ovaries were maintained in culture for four days before a single exposure to vehicle control (1% DMSO; CT) or DMBA (12nM; low-concentration or 75nM; high-concentration). After four or eight additional days of culture, DMBA-induced follicle depletion was evaluated via follicle enumeration. Relative to control, DMBA did not affect follicle numbers after 4days of exposure, but induced large primary follicle loss at both concentrations after 8days; while, the low-concentration DMBA also caused secondary follicle depletion. Neither concentration affected primordial or small primary follicle number. RNA was isolated and quantitative RT-PCR performed prior to follicle loss to measure mRNA levels of genes involved in xenobiotic metabolism (Cyp2e1, Gstmu, Gstpi, Ephx1), autophagy (Atg7, Becn1), oxidative stress response (Sod1, Sod2) and the phosphatidylinositol 3-kinase (PI3K) pathway (Kitlg, cKit, Akt1) 1, 2 and 4days after exposure. With the exception of Atg7 and cKit, DMBA increased (P<0.05) expression of all genes investigated. Also, BECN1 and pAKTThr308 protein levels were increased while cKIT was decreased by DMBA exposure. Taken together, these results suggest an increase in DMBA bioactivation, add to the mechanistic understanding of DMBA-induced ovotoxicity and raise concern regarding female low concentration DMBA exposures.

Original languageEnglish (US)
Pages (from-to)179-187
Number of pages9
JournalToxicology and Applied Pharmacology
Volume276
Issue number3
DOIs
StatePublished - May 1 2014

Fingerprint

9,10-Dimethyl-1,2-benzanthracene
Gene expression
Rats
Ovary
Gene Expression
anthracene
Genes
Phosphatidylinositol 3-Kinase
Oxidative stress
Ovarian Follicle
Polycyclic Aromatic Hydrocarbons
Autophagy
Inbred F344 Rats
Xenobiotics
Dimethyl Sulfoxide
Metabolism
Smoke
Tobacco Products
Biological materials
Oxidative Stress

Keywords

  • DMBA
  • Follicle
  • Ovary

ASJC Scopus subject areas

  • Pharmacology
  • Toxicology

Cite this

Acute 7,12-dimethylbenz[a]anthracene exposure causes differential concentration-dependent follicle depletion and gene expression in neonatal rat ovaries. / Madden, Jill A.; Hoyer, Patricia B; Devine, Patrick J.; Keating, Aileen F.

In: Toxicology and Applied Pharmacology, Vol. 276, No. 3, 01.05.2014, p. 179-187.

Research output: Contribution to journalArticle

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