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Restoration of Dioxin-Induced Damage to Fetal Steroidogenesis and Gonadotropin Formation by Maternal Co-Treatment with α-Lipoic Acid

机译:通过母体与α-硫辛酸的共同治疗恢复二恶英对胎儿类固醇生成和促性腺激素形成的损害

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摘要

2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD), an endocrine disruptor, causes reproductive and developmental toxic effects in pups following maternal exposure in a number of animal models. Our previous studies have demonstrated that TCDD imprints sexual immaturity by suppressing the expression of fetal pituitary gonadotropins, the regulators of gonadal steroidogenesis. In the present study, we discovered that all TCDD-produced damage to fetal production of pituitary gonadotropins as well as testicular steroidogenesis can be repaired by co-treating pregnant rats with α-lipoic acid (LA), an obligate co-factor for intermediary metabolism including energy production. While LA also acts as an anti-oxidant, other anti-oxidants; i.e., ascorbic acid, butylated hydroxyanisole and edaravone, failed to exhibit any beneficial effects. Neither wasting syndrome nor CYP1A1 induction in the fetal brain caused through the activation of aryl hydrocarbon receptor (AhR) could be attenuated by LA. These lines of evidence suggest that oxidative stress makes only a minor contribution to the TCDD-induced disorder of fetal steroidogenesis, and LA has a restorative effect by targeting on mechanism(s) other than AhR activation. Following a metabolomic analysis, it was found that TCDD caused a more marked change in the hypothalamus, a pituitary regulator, than in the pituitary itself. Although the components of the tricarboxylic acid cycle and the ATP content of the fetal hypothalamus were significantly changed by TCDD, all these changes were again rectified by exogenous LA. We also provided evidence that the fetal hypothalamic content of endogenous LA is significantly reduced following maternal exposure to TCDD. Thus, the data obtained strongly suggest that TCDD reduces the expression of fetal pituitary gonadotropins to imprint sexual immaturity or disturb development by suppressing the level of LA, one of the key players serving energy production.
机译:2,3,7,8-四氯二苯并-对-二恶英(TCDD)是一种内分泌干扰物,在许多动物模型中,母体暴露后会引起幼崽的生殖和发育毒性。我们以前的研究表明,TCDD通过抑制胎儿垂体促性腺激素(性腺类固醇生成的调节剂)的表达来标记性不成熟。在本研究中,我们发现,TCDD对妊娠大鼠与α-硫辛酸(LA)的共同治疗可以修复所有TCDD对胎儿垂体促性腺激素产生的损害以及睾丸类固醇的生成。包括能源生产。洛杉矶还起着抗氧化剂的作用,其他抗氧化剂也可以。即抗坏血酸,丁基化羟基茴香醚和依达拉奉未能表现出任何有益作用。 LA不能减弱因芳基烃受体(AhR)激活而引起的胎儿大脑消耗综合征或CYP1A1诱导。这些证据表明,氧化应激仅对TCDD诱导的胎儿类固醇生成紊乱做出了很小的贡献,而LA通过靶向除AhR激活以外的其他机制而具有修复作用。经过代谢组学分析,发现TCDD引起的垂体下丘脑下丘脑变化比垂体本身更明显。尽管三羧酸循环的成分和胎儿下丘脑的ATP含量被TCDD显着改变,但所有这些改变都被外源性LA纠正。我们还提供了证据,表明孕妇暴露于TCDD后内源性LA的胎儿下丘脑含量显着降低。因此,获得的数据有力地表明,TCDD通过抑制LA的水平而降低了胎儿垂体促性腺激素的表达,从而压制了性不成熟或干扰了发育,LA是产生能量的关键因素之一。

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