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首页> 外文期刊>Environmental Pollution >First evidence of the protective role of melatonin in counteracting cadmium toxicity in the rat ovary via the mTOR pathway
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First evidence of the protective role of melatonin in counteracting cadmium toxicity in the rat ovary via the mTOR pathway

机译:褪黑素催化作用MTOR途径在大鼠卵巢中镉毒性的第一种证据

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摘要

Herein, the first evidence of the ability of melatonin (MLT) to counteract cadmium (Cd) toxic effects on the rat ovary is reported. Cd treatment, enhancing oxidative stress, provoked clear morphological, histological and biomolecular alterations, i.e. in the estrous cycle duration, in the ovarian and serum E-2 concentration other than in the steroidogenic and folliculogenic genes expression. Results demonstrated that the use of MLT, in combination with Cd, avoided the changes, strongly suggesting that it is an efficient antioxidant for preventing oxidative stress in the rat ovary. Moreover, to explore the underlying mechanism involved, at molecular level, in the effects of Cd-MLT interaction, the study focused on the mTOR and ERK1/2 pathways. Interestingly, data showed that Cd influenced the phosphorylation status of mTOR, of its downstream effectors and of ERK1/2, inducing autophagy and apoptosis, while cotreatment with MLT nullified these changes. This work highlights the beneficial role exerted by MLT in preventing Cd-induced toxicity in the rat ovary, encouraging further studies to confirm its action on human ovarian health with the aim to use this indolamine to ameliorate oocyte quality in women with fertility disorders. (C) 2020 Elsevier Ltd. All rights reserved.
机译:这里,报道了褪黑素(MLT)抵消镉(CD)对大鼠卵巢毒性作用的能力的第一种证据。 CD处理,增强氧化应激,引起明确的形态学,组织学和生物分子改变,即在卵巢和血清中血清持续时间,除了在类固化性和卵泡基因的表达中的卵巢和血清E-2浓度。结果表明,使用MLT与CD组合避免了变化,强烈表明它是预防大鼠卵巢中氧化应激的有效抗氧化剂。此外,为了探讨CD-MLT相互作用的分子水平所涉及的潜在机制,该研究集中于MTOR和ERK1 / 2途径。有趣的是,CD的数据显示CD影响其下游效应器和ERK1 / 2的MTOR的磷酸化状态,诱导自噬和细胞凋亡,而MLT的分圈无效这些变化。这项工作凸显了MLT在预防大鼠卵巢中诱导的毒性,令人鼓舞的进一步研究以确认其对人类卵巢健康的行动,以利用这种吲哚胺来改善具有生育障碍的妇女的卵母细胞质量的进一步研究。 (c)2020 elestvier有限公司保留所有权利。

著录项

  • 来源
    《Environmental Pollution》 |2021年第2期|116056.1-116056.10|共10页
  • 作者单位

    Univ Monastir Inst Super Biotechnol Monastir Lab LR11ES41 Genet Biodiversite & Valorisat Biore Monastir Tunisia;

    Univ Campania Luigi Vanvitelli Sez Fisiol Umana & Funz Biol Integrate F Bottazzi Dipartimento Med Sperimentale Via Costantinopoli 16 I-80138 Naples Italy;

    Univ Monastir Inst Super Biotechnol Monastir Lab LR11ES41 Genet Biodiversite & Valorisat Biore Monastir Tunisia;

    Wroclaw Med Univ Dept Human Morphol & Embryol Div Histol & Embryol Wroclaw Poland;

    Wroclaw Med Univ Dept Human Morphol & Embryol Div Histol & Embryol Wroclaw Poland;

    Univ Monastir Inst Super Biotechnol Monastir Lab LR11ES41 Genet Biodiversite & Valorisat Biore Monastir Tunisia;

    UT Hlth Sci Ctr Dept Cellular & Struct Biol San Antonio TX USA;

    Univ Campania Luigi Vanvitelli Sez Fisiol Umana & Funz Biol Integrate F Bottazzi Dipartimento Med Sperimentale Via Costantinopoli 16 I-80138 Naples Italy;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Melatonin; Cadmium toxicity; Oxidative stress; Autophagy; mTOR pathway; Endocrine disruptor;

    机译:褪黑素;镉毒性;氧化应激;自噬;MTOR途径;内分泌干扰器;

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