• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

环境砷暴露与雌雄生殖系统毒性及缓解策略:综述。

Environmental arsenic exposure and reproductive system toxicity in male and female and mitigatory strategies: a review.

机构信息

Occupational Environment Research Center, Rafsanjan University of Medical Sciences, Rafsanjan, Iran.

Department of Environmental Health Engineering, School of Health, Occupational Safety and Health Research Center, NICICO, World Safety Organization and Rafsanjan University of Medical Sciences, Rafsanjan, Iran.

出版信息

Environ Geochem Health. 2024 Sep 13;46(10):420. doi: 10.1007/s10653-024-02197-8.

DOI:10.1007/s10653-024-02197-8
PMID:39269655
Abstract

Environmental Arsenic (As) exposure is one of the main health challenges in different area of the world. As is a significant factor responsible to the reproductive system toxicity in both male and female. In this study, the most important effects mechanisms and biomarkers related to environmental exposure to As and the reproductive system toxicity, and infertility risk are reviewed in male and female. The results showed that the most important As-induced reproductive system toxicity in the male were alteration in the quantity and quality of semen, testicular toxicity, oxidative stress, testosterone reduction, and sperm apoptosis. For female were oxidative stress, spontaneous miscarriage, reproductive cycle disruption, decrease in the estradiol, progesterone, and testosterone levels and impair fecundity. The main mechanisms of reproductive system toxicity caused by As exposure in male were, genotoxic effects, reduction of glutathione, disruption of sex hormones, sperm flagellum formation impairment, inhibition of spermatogenesis, disruption of cell signaling pathways, and metabolites disruption. For female were abnormal signaling in gene expression, hormonal homeostasis, As-accumulation in placental tissue and creation of reactive oxygen, disruption in the neurotransmitters balance, and sex hormones disruption. The suitable biomarkers for As-induced reproductive toxicity in male were changes in testosterone, one-carbon and lipid metabolism, noncoding RNAs, and steroid hormone homeostasis, and for female was human chorionic gonadotropin (hCG) changes. Finaly, taking selenium, zinc, silymarin, vitamins (C and E) and phytonutrients can be effective in reducing the As-induced reproductive system toxicity and infertility risk.

摘要

环境砷(As)暴露是世界不同地区的主要健康挑战之一。As 是导致男性和女性生殖系统毒性和不孕风险的重要因素。在这项研究中,综述了与环境暴露于 As 相关的生殖系统毒性和不孕风险的最重要的作用机制和生物标志物。结果表明,As 对男性生殖系统毒性的最重要影响是精液数量和质量的改变、睾丸毒性、氧化应激、睾酮减少和精子凋亡。对女性而言,是氧化应激、自然流产、生殖周期紊乱、雌二醇、孕酮和睾酮水平下降以及生育能力受损。As 暴露引起男性生殖系统毒性的主要机制是遗传毒性作用、谷胱甘肽减少、性激素破坏、精子鞭毛形成受损、精子发生抑制、细胞信号通路破坏和代谢物破坏。对于女性,是基因表达异常信号、激素平衡、胎盘组织中 As 积累和活性氧的产生、神经递质平衡的破坏以及性激素的破坏。男性中适合 As 诱导的生殖毒性的生物标志物是睾酮、一碳和脂质代谢、非编码 RNA 和类固醇激素动态平衡的变化,而女性则是人绒毛膜促性腺激素(hCG)的变化。最后,服用硒、锌、水飞蓟素、维生素(C 和 E)和植物营养素可以有效降低 As 引起的生殖系统毒性和不孕风险。

相似文献

1
Environmental arsenic exposure and reproductive system toxicity in male and female and mitigatory strategies: a review.环境砷暴露与雌雄生殖系统毒性及缓解策略:综述。
Environ Geochem Health. 2024 Sep 13;46(10):420. doi: 10.1007/s10653-024-02197-8.
2
Current mechanistic perspectives on male reproductive toxicity induced by heavy metals.当前重金属诱导男性生殖毒性的机制观点。
J Environ Sci Health C Toxicol Carcinog. 2020;38(3):204-244. doi: 10.1080/26896583.2020.1782116. Epub 2020 Jul 10.
3
Review on molecular and biochemical insights of arsenic-mediated male reproductive toxicity.砷介导的雄性生殖毒性的分子和生化研究进展综述。
Life Sci. 2018 Nov 1;212:37-58. doi: 10.1016/j.lfs.2018.09.045. Epub 2018 Sep 27.
4
Arsenic-Induced Sex Hormone Disruption: An Insight into Male Infertility.砷诱导的性激素紊乱:对男性不育症的深入洞察。
Adv Exp Med Biol. 2022;1391:83-95. doi: 10.1007/978-3-031-12966-7_6.
5
Review on arsenic-induced toxicity in male reproductive system and its amelioration.砷对男性生殖系统的毒性作用及其改善的综述。
Andrologia. 2017 Nov;49(9). doi: 10.1111/and.12791. Epub 2017 Jan 30.
6
Unraveling the anti-androgenic mechanism of tris(2,3-dibromopropyl) isocyanurate (TBC) via the non-classical testosterone pathway and steroidogenesis: Potential human reproductive health implications.揭示三(2,3-二溴丙基)异氰尿酸酯(TBC)通过非经典睾酮途径和类固醇生成的抗雄激素作用机制:对人类生殖健康的潜在影响。
Chemosphere. 2024 Sep;363:142802. doi: 10.1016/j.chemosphere.2024.142802. Epub 2024 Jul 10.
7
Reproductive toxicity of low-level lead exposure in men.男性低水平铅暴露的生殖毒性
Environ Res. 2007 Oct;105(2):256-66. doi: 10.1016/j.envres.2007.05.011. Epub 2007 Jul 16.
8
Reproductive toxicity and related mechanisms of micro(nano)plastics in terrestrial mammals: Review of current evidence.微(纳)塑料对陆地哺乳动物的生殖毒性及其相关机制:当前证据综述。
Ecotoxicol Environ Saf. 2024 Jul 1;279:116505. doi: 10.1016/j.ecoenv.2024.116505. Epub 2024 May 28.
9
Generating adverse outcome pathway (AOP) of inorganic arsenic-induced adult male reproductive impairment via integration of phenotypic analysis in comparative toxicogenomics database (CTD) and AOP wiki.通过整合表型分析比较毒理学基因组数据库(CTD)和 AOP 维基,生成无机砷诱导成年雄性生殖损伤的不良结局途径(AOP)。
Toxicol Appl Pharmacol. 2021 Jan 15;411:115370. doi: 10.1016/j.taap.2020.115370. Epub 2020 Dec 15.
10
Reproductive toxicity of PFOA, PFOS and their substitutes: A review based on epidemiological and toxicological evidence.全氟辛酸(PFOA)、全氟辛烷磺酸(PFOS)及其替代品的生殖毒性:基于流行病学和毒理学证据的综述。
Environ Res. 2024 Jun 1;250:118485. doi: 10.1016/j.envres.2024.118485. Epub 2024 Feb 17.

引用本文的文献

1
Identification of hypoxia-related diagnostic biomarkers and immune signatures in diminished ovarian reserve.卵巢储备功能减退中缺氧相关诊断生物标志物及免疫特征的鉴定
Front Genet. 2025 Aug 4;16:1626992. doi: 10.3389/fgene.2025.1626992. eCollection 2025.
2
Unveiling the nexus between environmental exposures and testicular damages: revelations from autophagy and oxidative stress imbalance.揭示环境暴露与睾丸损伤之间的联系:自噬和氧化应激失衡的启示
Cell Death Discov. 2025 May 29;11(1):258. doi: 10.1038/s41420-025-02543-4.