Rescue effects of prenatal melatonin administration against bisphenol A- induced perturbations of reproductive and thyroid activities in male rat offsprings

Kamel M A Hassanin, S. Ibrahim, A. Abdel-Wahab, Dina M M H El-Kossi, A. H. Abdel-Razik
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Abstract

The current study aimed to investigate the effects of prenatal melatonin “MLT” administration against bisphenol A “BPA”- induced infertility and thyroid dysfunction in male rat offsprings (First generation “F1”). For that purpose, fifty adult albino rats (40 females and 10 males) were used and classified equally into five groups (8 females and 2 males in each group). First group (control group) in which, pregnant rats were injected with 0.3 ml of vehicle /day. The second group (low dose BPA) where rats received a daily dose of 25 µg / kg B.W. The third group (high dose BPA) where rats received a daily dose of 250 µg / kg B.W. Fourth group (low dose BPA + MLT) where rats received a daily dose of 25 µg BPA /kg B.W. plus 10 mg MLT / Kg B.W. The fifth group (high dose BPA + MLT) where the rats received a daily dose of 250 µg BPA / kg B.W. plus 10 mg /Kg B.W. All rats within each group received their specific treatment daily with subcutaneous injection starting from the fourth day of pregnancy till full term. Then, the male offsprings of each group were selected and reared until the 60th day after birth. Serum and tissue samples were collected for analyses and microscopical examination. Although prenatal administration of both BPA doses didn’t affect the body weight gain and testicular weights of male offsprings, they reduced significantly the serum levels of testosterone and triodotyrosine when compared to the control group. Also, both BPA doses disturb significantly the oxidant/antioxidant ratio. Moreover, prenatal administration of both BPA doses affected negatively semen quality of the produced offsprings and induced marked histological alterations in their testes and prostate. Remarkably, all serological and histological alterations observed after BPA exposure were ameliorated significantly with MLT co-administration. Thus, prenatal MLT administration could be considered an optimal treatment to relieve many reproductive disorders, degenerative changes of testes and prostate and thyroid malfunction induced in male offsprings after gestational exposure of their dams to BPA.
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产前给药褪黑素对双酚A诱导的雄性大鼠后代生殖和甲状腺活动紊乱的拯救作用
本研究旨在探讨产前给药褪黑激素(MLT)对双酚A (BPA)诱导的雄性大鼠后代(第一代“F1”)不育和甲状腺功能障碍的影响。为此,50只成年白化大鼠(雌性40只,雄性10只)被分为5组(每组8只雌性和2只雄性)。第一组(对照组)妊娠大鼠每天注射0.3 ml载药;第二组(低剂量双酚a)老鼠收到了25日剂量µg / kg B.W.第三组(高剂量双酚a)老鼠收到每日剂量的250µg / kg B.W.第四组(低剂量双酚a + MLT)在大鼠收到了25日剂量µg BPA MLT B.W. + 10毫克/公斤/公斤B.W.五组(高剂量双酚a + MLT)的老鼠每天收到250µg BPA B.W. + 10毫克/公斤/公斤B.W.每组内的所有老鼠收到具体的日常与皮下注射治疗从怀孕第四天开始直到足月。然后选取各组雄性后代,饲养至出生后第60天。收集血清和组织样本进行分析和显微镜检查。尽管产前注射两种双酚a剂量对雄性后代的体重增加和睾丸重量没有影响,但与对照组相比,它们显著降低了血清中睾酮和三碘酪氨酸的水平。此外,两种双酚a剂量都会显著扰乱氧化剂/抗氧化剂的比例。此外,两种BPA剂量的产前处理均对后代的精液质量产生负面影响,并诱导其睾丸和前列腺的组织学改变。值得注意的是,在双酚a暴露后观察到的所有血清学和组织学改变在MLT联合给药后显著改善。因此,产前给药可以被认为是一种最佳的治疗方法,以减轻许多生殖疾病,睾丸退行性改变,前列腺和甲状腺功能障碍的男性后代在妊娠期暴露于BPA。
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