Department of Animal Science, Iowa State University, Ames, IA 50011, USA.
Department of Physiology, University of Arizona, Tucson, AZ 85724, USA.
Toxicol Appl Pharmacol. 2014 May 1;276(3):179-87. doi: 10.1016/j.taap.2014.02.011. Epub 2014 Feb 24.
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 (75 nM) and has not (12.5 nM) 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 (12 nM; low-concentration or 75 nM; 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 4 days of exposure, but induced large primary follicle loss at both concentrations after 8 days; 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 4 days after exposure. With the exception of Atg7 and cKit, DMBA increased (P < 0.05) expression of all genes investigated. Also, BECN1 and pAKT(Thr308) 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.
慢性暴露于多环芳烃 7,12-二甲基苯并[a]蒽(DMBA)会耗尽小鼠和大鼠所有类型的卵泡,这种效应在体外模型中得到了模拟,而 DMBA 是在有机物燃烧(包括香烟烟雾)过程中产生的。为了研究在急性 DMBA 暴露期间卵泡耗竭涉及的机制,研究了两种浓度的 DMBA,其中一种浓度(75 nM)观察到卵泡耗竭,另一种浓度(12.5 nM)未观察到卵泡耗竭。在对新生 4 天的 F344 大鼠卵巢进行为期 4 天的培养后,用 vehicle control(1% DMSO;CT)或 DMBA(12 nM;低浓度或 75 nM;高浓度)进行单次处理。在培养 4 或 8 天后,通过卵泡计数评估 DMBA 诱导的卵泡耗竭。与对照相比,DMBA 在暴露 4 天后不影响卵泡数量,但在 8 天后两种浓度均导致大的初级卵泡丢失;而低浓度的 DMBA 也导致次级卵泡耗竭。两种浓度均不影响原始卵泡或小初级卵泡数量。在卵泡丢失之前分离 RNA 并进行定量 RT-PCR,以测量参与外源性代谢(Cyp2e1、Gstmu、Gstpi、Ephx1)、自噬(Atg7、Becn1)、氧化应激反应(Sod1、Sod2)和磷脂酰肌醇 3-激酶(PI3K)途径(Kitlg、cKit、Akt1)的基因的 mRNA 水平,暴露后 1、2 和 4 天进行测量。除了 Atg7 和 cKit 之外,DMBA 增加了(P < 0.05)所有研究基因的表达。此外,DMBA 暴露增加了 BECN1 和 pAKT(Thr308)蛋白水平,同时降低了 cKIT 水平。综上所述,这些结果表明 DMBA 的生物活化增加,有助于深入了解 DMBA 诱导的卵毒性,并引起对女性低浓度 DMBA 暴露的关注。